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International Journal of Carbohydrate Chemistry
Volume 2013 (2013), Article ID 624967, 14 pages
Production Methods for Hyaluronan
1Wageningen UR Food & Biobased Research, P.O. Box 17, 6700 AA Wageningen, The Netherlands
2Universitatea “Aurel Vlaicu,” Str. E. Dragoi nr. 2, 310330 Arad, Romania
3Genencor International B.V., P.O. Box 218, 2300 AE Leiden, The Netherlands
Received 29 November 2012; Accepted 21 January 2013
Academic Editor: Thomas J. Heinze
Copyright © 2013 Carmen G. Boeriu et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Hyaluronan is a polysaccharide with multiple functions in the human body being involved in creating flexible and protective layers in tissues and in many signalling pathways during embryonic development, wound healing, inflammation, and cancer. Hyaluronan is an important component of active pharmaceutical ingredients for treatment of, for example, arthritis and osteoarthritis, and its commercial value far exceeds that of other microbial extracellular polysaccharides. Traditionally hyaluronan is extracted from animal waste which is a well-established process now. However, biotechnological synthesis of biopolymers provides a wealth of new possibilities. Therefore, genetic/metabolic engineering has been applied in the area of tailor-made hyaluronan synthesis. Another approach is the controlled artificial (in vitro) synthesis of hyaluronan by enzymes. Advantage of using microbial and enzymatic synthesis for hyaluronan production is the simpler downstream processing and a reduced risk of viral contamination. In this paper an overview of the different methods used to produce hyaluronan is presented. Emphasis is on the advancements made in the field of the synthesis of bioengineered hyaluronan.
Hyaluronic acid, also known as hyaluronan, is a linear polysaccharide composed of a repeating disaccharide unit of β(1,4)-glucuronic acid (GlcUA)-β(1,3)-N-acetylglucosamine (GlcNAc) (Figure 1). Both individual carbohydrate residues in hyaluronan adopt the stable chair conformation which determines the conformation of the polymer in solution that is described as an overall random coil structure that may have also highly flexible regions. Nevertheless, in terms of chemical structure, hyaluronan is a simple linear polymer with high molecular mass and exceptional rheological properties. Hyaluronan is a member of the glycosaminoglycans family that includes chondroitin/dermatan sulfate, keratan sulfate, and heparin/heparan sulfate, each with a characteristic disaccharide-repeating structure of an amino sugar, either glucosamine or galactosamine, and a hexose, either galactose, glucuronic acid, or iduronic acid, which can be carboxylated or sulfated . Hyaluronan is the only glycosaminoglycan member that is not sulfated and is not covalently bound to a proteoglycan core protein.
Research on hyaluronan expands over more than one century (Table 1). The first report that can be linked to hyaluronan dates from 1880, when the French chemist Portes observed that the mucin in the vitreous body, which he named “hyalomucine,” behaved differently from other mucoids in cornea and cartilage. Fifty-four years later Meyer and Palmer described a procedure for isolating a novel glycosaminoglycan from the vitreous of bovine eyes, which they named hyaluronic acid based on hyaloid (vitreous) and uronic acid . Since in vivo the polymer exists in an ionized form as polyanion, it is generally referred to as hyaluronan.
In living organisms, hyaluronan is produced by hyaluronan synthase enzymes, which synthesize large, linear polymers of the repeating disaccharide β(1,4)-GlcUA-β(1,3)-GlcNAc by alternate addition of GlcUA and GlcNAc to the growing chain using their activated nucleotide sugars (UDP-glucuronic acid and UDP-N-acetylglucosamine) as substrates. The number of repeat disaccharides, , in a completed hyaluronan molecule is approximately 10,000 but chains of hyaluronan with up to 25,000 disaccharide units have been reported. The size of the polymers ( from 5,000 Da to 20 million Da) in vivo varies with the type of tissue. For example, hyaluronan in the human umbilical cord has a molecular mass of 3-4 million Da, whilst the molecular mass of hyaluronan from human synovial fluid is 6 million Da. However, the reported molecular weight of isolated hyaluronan polymers may be underestimated, depending on the isolation and analysis method used. Hyaluronan is not monodisperse in molecular weight and the experimentally determined polydispersity () of the polymer depends as well on both the method of extraction and the method of analysis used. For example, the values of the polydispersity of a hyaluronan sample determined by high-performance liquid chromatography varied with the type of column, the detection method, and the flow rate used [11–13]. This results in a big variation of the values reported for the and polydispersity of hyaluronan between laboratories and shows the importance for standardization of the methodology for characterization and reporting of hyaluronan molecular properties.
Hyaluronan is present in all vertebrates. High concentrations are found in the umbilical cord, the synovial fluid between joints, skin, and the vitreous body of the eye. It was estimated that in the body of a person of 70 kg, about 15 g hyaluronan is found in different tissues, of which one third is turned over every day. The human skin contains over 50% of the hyaluronan in the body [14, 15]. Rooster combs contain the highest concentrations of hyaluronan (7.5 mg g−1) ever reported for animal tissues . Hyaluronan is also present in the capsule of a small number of microbial pathogens such as Pasteurella multocida and group A and C streptococci among which Streptococcus pyogenes (a human pathogen) and the animal pathogens Streptococcus equi and Streptococcus uberis, that quite likely pirated the enzymatic machinery from vertebrate hosts for its synthesis. These microorganisms use hyaluronan to encapsulate their cells, forming a perfect disguise against the animal defense system and facilitating the adhesion and colonization of the bacterial cells . Since the hyaluronan polymer produced in animals and the aforementioned bacteria is identical, the host immune defense is not triggered to repel the pathogenic bacteria contrary to other bacteria with a different extracellular capsule. Intriguingly, the nonimmunogenic and noninflammatory properties of bacterial hyaluronan benefit mammals currently too, since bacterial hyaluronan forms an excellent source for medical grade hyaluronan. Initially hyaluronan was believed to be an inert compound having no specific interaction with other macromolecules. However, from the discovery of the interaction of hyaluronan with cartilage proteoglycans by Hardingham and Muir  a large number of reports have been published on the role of hyaluronan in cellular activity, migration, mitosis, inflammation, cancer, angiogenesis, fertilization, and so on (see for more information [19, 20]).
In addition, hyaluronan and its derivatives have been largely studied and applied in the biomedical field (Table 2) [21–23]. Due to the high level of biocompatibility, hyaluronan is extensively used in viscosurgery, in the treatment of arthritis to supplement the lubrication of arthritic joints, as microcapsule for targeted drug delivery and in cosmetics as a hydrating and antiaging material.
The biological functions of hyaluronan are strongly depending upon its size. High molecular weight hyaluronan polymers ( Da) are space filling, antiangiogenic, and immunosuppressive; medium size hyaluronan chains ( between 2 × 104–105 Da) are involved in ovulation, embryogenesis, and wound repair; oligosaccharides with 15–50 repeating disaccharide units ( between 6 × 103–2 × 104 Da) are inflammatory, immuno-stimulatory, and angiogenic while small hyaluronan oligomers ( from 400 to 4000 Da) are anti-apoptotic and inducers of heat shock proteins . Lower molecular weight hyaluronan and small oligosaccharides are produced by controlled depolymerization of high molecular weight hyaluronan using physical treatment (thermal treatment, pressure), irradiation (electron beam, gamma ray, microwave), acid treatment, ozonolysis, metal catalyzed radical oxidation, and enzymatic hydrolysis with hyaluronidase (EC 18.104.22.168).
The commercial value of hyaluronan far exceeds that of other microbial extracellular polysaccharides. With an estimated world market value of $US 500 million, it is sold for up to $US 100,000 per kilogram . On top of this, several groups have reported effects of hyaluronan oligosaccharides on cellular behavior that could imply the use of these molecules in cancer treatment or in wound healing . It is clear that hyaluronan is much more than a space-filling inert component of the extracellular matrix and will become more and more important as a pharmaceutical component and indeed is a multifunctional megadalton stealth molecule . In this paper the different methods to produce hyaluronan will be discussed as depicted in Figure 2.
2. Biosynthetic Pathways for Hyaluronan in Living Organisms
The overall reaction of hyaluronan synthesis is as follows:
The reaction is catalyzed by a single enzyme utilizing both sugar substrates to synthesize hyaluronan . In contrast to other glycoaminoglycans which are synthesized in the Golgi network, hyaluronan is synthesized at the plasma membrane [29, 30]. Hyaluronan synthases (EC 22.214.171.124) are predicted to have multiple membrane spanning domains with a large intracellular loop on the plasma membrane’s inner face. The only known exception is the P. multocida hyaluronan synthase which has a membrane attachment domain near the carboxyl terminus. Hyaluronan molecules are extruded into the extracellular matrix in coordination with their synthesis , but they also exist intracellularly. In the extracellular matrix hyaluronan exists in a number of different forms. For example, in vertebrates it can be intercalated within a proteoglycan complex, referred to glycocalyx if it is a more delicate pericellular matrix, or it can be bound to membrane receptors of the cell surface. It can interact with binding proteins so-called hyaladherins, which is also the case for intracellular hyaluronan . The mechanisms regulating extracellular versus intracellular location of hyaluronan are not known yet. Recently, the presence of hyaluronan cables has been reported that was the result of the incorporation of the heavy chain of interalpha-trypsin inhibitor with hyaluronan . Depending on the type of tissue, different hyaluronan concentrations and molecular weight evoke different cell responses, for example, during embryonic development, healing processes, inflammation, and cancer. How the cell response is influenced by the different molecular weight of hyaluronan is still an intriguing question [15, 24].
In 1996 the first reports were published concerning the cloning of mammalian hyaluronan synthases [33, 34]. Since then in human cells three hyaluronan synthase genes have been found encoding enzymes having distinct enzymatic properties with respect to hyaluronan size and size distribution  which are differentially inducible by growth factors and cytokines [36, 37].
In 1993 the first gene encoding the enzyme responsible for hyaluronan synthesis, denoted HA synthase or HAS, was identified from group A streptococci [6, 7]. This gene is part of an operon containing the hasA gene encoding hyaluronan synthase, the hasB gene encoding UDP-Glucose dehydrogenase, and the hasC gene encoding UDP-Glucose-pyrophosphorylase [38–40]. A hydropathy plot of the hasA gene predicts three transmembrane segments which is in accordance with the early findings of Markovitz and coworkers who showed that the hyaluronan synthase activity is located in the cell membrane of streptococci . Cloning of the group A and later the group C streptococcal hyaluronan synthase genes  allowed researchers to confirm that only one gene product (the HA-synthase protein) is required for hyaluronan biosynthesis.
The first vertebrate gene identified as being HA synthase was the Xenopus laevis gene DG42 . Since then more vertebrate HA synthase genes were identified  and in addition an HA synthase from an algal virus was discovered [17, 45]. The streptococcal, vertebrate, and viral HA synthases show protein sequence similarity and appear to have a single glycosyl transferase 2 (GT2) family module  with some similarities to chitin synthase. The last extension of organisms in which a HA synthase gene was identified is Cryptococcus neoformans. The CPS1 gene from this pathogenic yeast encodes a HA synthase with high homology to the previously mentioned HA synthase proteins . An HA synthase that differs in protein sequence and in predicted topology from all other HA synthases was identified and cloned from type A P. multocida, an animal pathogen .
Unlike the other HA synthases (Table 3; grouped as Class I HA synthases) which are integral membrane proteins and elongate hyaluronan chains at the reducing end (Class I-R) or at the nonreducing end , the P. multocida HA synthase has a membrane attachment domain near the carboxyl terminus, has two GT2 modules, and elongates the HA chains at the nonreducing end. It is therefore called a Class II HA synthase . So far the P. multocida HA synthase is the only known member of the Class II HA synthases [49, 51, 52].
The regulation of hyaluronan synthesis is much more complex in vertebrates than in bacteria because hyaluronan fulfills various functions in the mammalian body depending on the tissue involved and the hyaluronan chain length required. For the three mammalian HA synthase isozymes different expression patterns are observed between adult and embryonic tissues [54, 55]. Several regulatory factors are known to be involved in controlling HA synthase transcription, such as morphogenesis, cytokines, growth factors, and antisense mRNA [56, 57]. Furthermore, hyaluronan synthesis seems to be controlled through translation regulation, since a latent pool of HA synthase exits within the cell interior, in the endoplasmic reticulum-Golgi compartments, that upon insertion in the cell membrane becomes activated . HA synthase activity can be modulated by posttranslational modification, such as phosphorylation and N-glycosylation . Intermediate and small oligosaccharides are probably provided through hyaluronan cleavage by hyaluronidases, since mammalian HA synthase isozymes synthesize hyaluronan higher than 105 Da . Due to the high complexity of the regulation of hyaluronan synthesis in vertebrates a cohesive view on the relation between the regulatory components is not available yet.
Recently, the metabolic route of hyaluronan formation in S. zooepidemicus was elucidated. The streptococcal HA synthase is found in operons also encoding one or more enzymes involved in biosynthesis of the activated sugars . The has operon in S. zooepidemicus encodes for five genes (Figure 3): hyaluronan synthase (hasA), UDP-glucose dehydrogenase (hasB), UDP-glucose pyrophosphorylase (hasC), a glmU paralog encoding for a dual function enzyme acetyltransferase and pyrophosphorylase activity (hasD), and a pgi paralog encoding for phosphoglucoisomerase (hasE) . HasB and hasC are involved in UDP-GlcUA synthesis, while hasD and hasE are involved in the synthesis of UDP-GlcNAc. The hyaluronan biosynthesis is a costly process for bacteria in terms of carbon and energy resources and competes with cell growth because of the large pathway overlap with the cell wall biosynthesis (Figure 3). Other streptococci strains have has operons that contain besides hyaluronan synthase, only the hasB and hasC genes. This suggests that the superior hyaluronan synthesis observed for S. zooepidemicus relates to the availability of UDP-sugar precursors. Understanding the metabolic routes for hyaluronan synthesis had a significant role in the optimization of the microbial production of hyaluronan, allowing the control of the polymer chain length and increasing the product yield.
3. Production of Hyaluronan
Industrial manufacturing of hyaluronan is based on two main processes, the extraction from animal tissues and microbial fermentation using bacterial strains. Both technologies produce polydisperse high molecular weight hyaluronan ( Da, polydispersity ranging from 1.2 to 2.3) for biomedical and cosmetic applications [12, 61, 62]. The first process, to be applied at industrial scale, was the extraction of hyaluronan from animal waste which is still an important technology for commercial products, but is hampered by several technical limitations. One drawback in the extraction process is the inevitable degradation of hyaluronan, caused by (a) the endogenous hyaluronidase activity in animal tissues, breaking down the polymer chain through enzymatic hydrolysis, and (b) the harsh conditions of extraction. Extraction protocols have been improved over the years, but still suffer from low yields, due to the intrinsic low concentration of hyaluronan in the tissue, and from high polydispersity of polymer products due to both the natural polydispersity of hyaluronan and to the uncontrolled degradation during extraction. As in any process for the production of therapeutic compounds from animal sources, there is a potential risk of contamination with proteins and viruses, but this can be minimized by using tissues from healthy animals and extensive purification. Nevertheless, concerns on viral (particularly avian) and protein (particularly bovine) contamination increased the interest in the biotechnological production of hyaluronan.
Production of hyaluronan by bacterial fermentation evolved to a mature technology in the last two decades of the 20th century. In the early developmental stages of bacterial fermentation using group A and C streptococci, optimization of culture media and cultivation conditions along with strain improvement were used to increase hyaluronan yield and quality. Hyaluronan yields reached 6-7 g L−1, which is the upper technical limit of the process caused by mass transfer limitation due to the high viscosity of the fermentation broth. Bacterial fermentation produces hyaluronan with high molecular weight and purity, but risk of contamination with bacterial endotoxins, proteins, nucleic acids, and heavy metals exists. The identification of the genes involved in the biosynthesis of hyaluronan and of the sugar nucleotide precursors in the 90s opened the way towards hyaluronan production using safe, nonpathogenic recombinant strains.
In the past decade a new technology emerged using isolated HA synthase to catalyze the polymerization of the UDP-sugar monomers. This novel enzymatic technology for hyaluronan synthesis is very versatile allowing producing both high molecular weight hyaluronan and hyaluronan oligosaccharides with defined chain length and low polydispersity. Production of monodisperse hyaluronan oligosaccharides on mg-scale using two single-action mutants of the P. multocida HA synthase was demonstrated by the group of DeAngelis , but large scale production was not achieved yet. A comparative analysis of established and emerging technologies for high molecular weight hyaluronan production is given in Table 4.
3.1. Extraction from Animal Tissues
Extraction of hyaluronan from animal tissues was initially used for laboratory investigations in order to identify and characterize the polymer and to elucidate its biological potential and biomedical application. Hyaluronan from almost all tissues of vertebrates including the vitreous body of the eye, umbilical cord, synovial fluid, pig skin, the pericardial fluid of the rabbit, and the cartilage of sharks was isolated and described . Recently, the extraction of hyaluronan from fish eyes as an alternative resource outside animal husbandry was reported . Nevertheless, the most accessible sources for large scale production high molecular weight hyaluronan are rooster combs (1.2 × 106 Da), the human umbilical cords (3.4 × 106 Da), the vitreous humor of cattle (7.7 × 104–1.7 × 106 Da), and the bovine synovial fluid (14 × 106 Da).
Despite the numerous methods for isolation and purification of hyaluronan reported in the early literature, it was only in 1979 that a method became available for the production of pharmaceutical grade hyaluronan by extraction from animal tissues. Balazs  developed an efficient procedure to isolate and purify hyaluronic acid from rooster combs and human umbilical cords that set the basis of the industrial production of hyaluronan from rooster combs for medical application.
Hyaluronan is soluble in water, but extraction of highly pure, high molecular weight hyaluronan from animal tissues is difficult, since in biological materials hyaluronan is usually present in a complex with other biopolymers including proteoglycans . Methods to release hyaluronan from these complexes comprise the use of proteolytic enzymes (i.e., papain, pepsin, pronase, and trypsin), hyaluronan ion-pair precipitation (with e.g., cetylpyridinium chloride), precipitation with organic solvents, nonsolvent precipitation, detergents, and so forth . Ultrafiltration and chromatography are used to remove the degradation products and other contaminants. Sterile filtration is used to remove all microbial cells prior to alcohol precipitation, drying, and conditioning of the end product.
Despite extensive purification, animal hyaluronan can be contaminated with proteins and nucleic acids. The quantity and nature of contaminants differ with the source, as was shown for hyaluronan isolates from human umbilical cord and bovine vitreous humor, containing elevated protein and nucleic acid levels compared to those from rooster comb and bacterial capsule isolates . Diseases as bovine spongiform encephalopathy (BSE) made us aware of the risk of cross-species viral infection. Consequently, hyaluronan from animal sources has to be extensively purified to get rid of these contaminants and extraction and purification processes are continuously improved to fulfill the high quality standards for medical applications. To date, animal waste is still the most important source for the industrial manufacturing of hyaluronan for medical application and provides up to several tones of medical-grade hyaluronan preparations per year. Pharmacia (Sweden), Pfizer (USA), Genzyme (USA), and Diosynth (The Netherlands) were among the first companies that produced hyaluronan from animal waste at industrial scale. Commercially available hyaluronan preparations from animal sources have a molecular weight ranging from several hundred thousand up to 2.5 million Da .
3.2. Bacterial Production
The development of hyaluronan production through bacterial fermentation started in the 60s, when it was acknowledged that animal derived hyaluronan sources can contain undesired proteins causing possible allergic inflammation responses . Since the hyaluronan polymer produced in animals and bacteria is identical, bacterial hyaluronan is not immunogenic and therefore is an excellent source for medical grade hyaluronan. Extracting hyaluronan from microbial fermentation broth is a relatively simple process with high yields. An additional and important advantage of microbial hyaluronan production is that microbial cells can be physiologically and/or metabolically adapted to produce more hyaluronan of high molecular weight. Therefore, microbial hyaluronan production using either pathogenic streptococci or safe recombinant hosts, containing the necessary hyaluronan synthase, is nowadays more and more preferred.
3.2.1. Production of Hyaluronan with Streptococci Strains
The first reported hyaluronic acid isolation from group A hemolytic streptococci resulted in 60–140 mg L−1 hyaluronan . Since then, many different attempts have been made to increase the amount of hyaluronan, including traditional techniques as optimizing the extraction process, adapting the culture media, and selecting strains with high hyaluronan productivity. In thirty years, the hyaluronan yields using batch fermentation increased from 300–400 mg L−1  to 6-7 g L−1 , which is the practical limit due to mass transfer limitations . Group C streptococci which are not human pathogens and have superior hyaluronan productivity are frequently used for hyaluronan synthesis instead of Group A streptococci or instead the animal pathogenic bacterium P. multocida. The most used strains are S. equi subsp. equi and S. equi subsp. zooepidemicus. From dairy food products S. thermophilus strains with high productivity of useful exopolysaccharides including hyaluronan were isolated , offering a safe hyaluronan producing organism. Recently, a recombinant S. thermophilus was constructed that was able to produce 1.2 g L−1 hyaluronan and the average molecular weight was comparable with the wild type strain .
Streptococci strains for hyaluronan production generally use glucose as carbon source. The yield of hyaluronan on glucose under aerobic fermentation conditions varies between 5 and 10% [25, 73, 74], which is significantly higher than typical yields for complex polysaccharides in lactic acid bacteria. Other carbon sources like starch , lactose, sucrose, and dextrin  can be used for hyaluronan productivity similar to glucose. The use of carbon sources like starch and lactose which are largely available at lower costs is important in view of the process economics.
Research on optimization of hyaluronan production through fermentation of streptococci strains addressed the improvement of the hyaluronan yield, the increase of the molecular weight, and the reduction of the polymer polydispersity, parameters which are essential for hyaluronan applications. The main question was if the molecular weight could be further regulated either through strain improvements, optimized process conditions, or through metabolic engineering. These topics will be discussed below.
Regulation within Bacterial Cells. Energy and Carbon Resources. Hyaluronan biosynthesis in streptococci requires a large amount of energy and competes with the bacterial cell growth for glucose as energy provider or as UDP-sugar precursor. Indeed, when unlimited glucose is available, the highest bacterial growth was observed at optimal cultivation conditions (pH 7 and 37°C) whilst the highest hyaluronan productivity and molecular weight were obtained at suboptimal growth conditions, since when cells are growing slowly, the carbon and energy resources are available for other processes . Under glucose-limiting conditions first hyaluronan productivity and then molecular weight declines . Decrease of the initial glucose concentrations from 60 to 20 g L−1 decreased the hyaluronan concentration and molecular weight from 4.20 g L−1 and 3.0 million Dalton, to 1.65 g L−1 and 2.65 million Dalton, respectively .
Aerobic culturing conditions increased the hyaluronan productivity by 50% as well as hyaluronan molecular weight whereas cell growth was unaffected [77–79]. Under aerobic fermentation conditions streptococci change their metabolism from producing lactate into producing acetate, formate, and ethanol. This generates four ATP molecules per hexose for the acetate production instead of two ATP molecules formed in lactate production . It was assumed that the increase of hyaluronan production is due to the increased levels of ATP or to increased levels of NADH oxidase which removes the excess of NADH in the presence of oxygen. However, studies designed to improve ATP formation by increased acetate production through maltose metabolism  or increasing NADH oxidase levels by metabolic engineering  revealed that hyaluronan synthesis was not limited by energy resources.
Studies have shown that only a critical level of dissolved oxygen of 5% is needed to increase the hyaluronan yield during cell growth, above this value the yield is constant . Interestingly, the expression of HA synthase in S. zooepidemicus is nine times higher under aerobic conditions than under anaerobic conditions , explaining the increase of hyaluronan synthesis. Furthermore, oxygen induces enzymes involved in the production of UDP-GlcNAc (hasD) and acetoin recycling, which offers an additional ATP molecule and acetyl-CoA that can be used in hyaluronan production .
Based on these results, we can conclude that elevated HA synthase concentrations and UDP-GlcNAc availability seem to be the main reason for the increase in hyaluronan synthesis under aerobic conditions.
Influence of Process Conditions on Hyaluronan Yield and Molecular Weight. Streptococcal fermentation to produce hyaluronan is, like other fermentations, influenced by medium composition, pH, temperature, aeration, and agitation. Especially aerobic conditions and the initial glucose concentration had a large influence on hyaluronan yield and molecular weight, as was discussed above. Both agitation and fermentation modus have a rather complex effect on hyaluronan production and are, therefore, in greater detail described, below.
The effect of agitation on the yield and the molecular weight of hyaluronan in Streptococcus fermentation is complex. Increasing agitation increases the hyaluronan yield under both anaerobic and aerobic conditions, most probably due to an enhanced mass transfer induced by the reduced viscosity of the broth [77, 79, 83, 84]. However, hyaluronan molecular weight increases at moderate impeller speed due to mass transfer enhancement, but decreases at high impeller speed most probably due to degradation by the reactive oxygen species that are formed under aerobic conditions at high impeller speed . Oxidative degradation of hyaluronan can be prevented by the addition of oxygen scavengers such as salicylic acid in the culture media resulting in an increase of the hyaluronan molecular weight [85, 86].
Batch versus Chemostat. In batch fermentation, the hyaluronan production is limited to 6-7 g L−1 due to high viscosity of the broth and mass transfer constraints. Further improvement of the hyaluronan yield is therefore not possible through high-cell-density fermentation or through a high-yield strain. A continuous culture is the best strategy to improve the volumetric productivity of hyaluronan synthesis for four reasons. First, cell growth of streptococci can be maintained at the exponential phase. Extension of the exponential phase could lead to an increased amount of hyaluronan, since it was shown that hyaluronan synthesis stops in the stationary phase [40, 87] and the excretion of the HA synthase and other cell wall proteins which takes place in the stationary phase is prevented . Second, suboptimal growth conditions can be imposed by nutrient limitation in order to decrease the resource competition between cell growth and hyaluronan synthesis [77, 89]. Third, a turnaround phase is avoided by using a continuous culture . Finally, the viscosity of the broth can be controlled by controlling the hyaluronan concentration, thus enhancing the mass transfer in the reactor. Chemostat cultivation of S. zooepidemicus by controlling the medium conditions has been reported [75, 90, 91] and this opens the way for further improvement of the hyaluronan production process.
Strain Improvement. Improved hyaluronan producing strains have been obtained by random mutagenesis and selection of mutant strains oriented to the reduction of the hyaluronan-depolymerising enzyme responsible for the decrease of molecular weight of hyaluronan during fermentation (hyaluronidase-negative strains) and to the reduction of streptolysin, the exotoxin responsible for the β-hemolysis (nonhemolytic strains). Fermentation of nonhemolytic and hyaluronidase-free mutants produced hyaluronan with a molecular weight varying from 3.5 to 5.9 million Da and yields around 6-7 g L−1 [70, 76, 92]. Random mutagenesis has also resulted in Streptococci strains that produce hyaluronan of extraordinary high molecular weight ranging from 6 to 9 million Da and with moderate yields of 100 to 410 mg L−1 .
Further improvement of strains requires genetic engineering of the producer microorganisms to engineer the hyaluronan metabolic pathway. Metabolic engineering in S. zooepidemicus and in recombinant hosts has demonstrated that the ratio between UDP-GlcNAc and UDP-GlcUA and the ratio between HA synthase and substrates are the most important factors to influence hyaluronan molecular weight. Chen et al. individually overexpressed each of the five genes in the has operon in S. zooepidemicus. They discovered that overexpression of hasA, involved in hyaluronan biosynthesis, and hasB and hasC, involved in UDP-GlcUA biosynthesis, decreased molecular weight, while overexpression of hasE, involved in UDP-GlcNAc biosynthesis, greatly enhanced molecular weight. Overexpression of hasD had no effect, but molecular weight was further increased when combined with hasE overexpression . Upregulation of hasD in S. zooepidemicus has been observed at aerobic conditions  but also in the presence of an empty plasmid , both accompanied by a production of higher hyaluronan. Marcellin et al.  suggested that regulation of hasD is at the translational or posttranslational level and that the plasmid burden is sufficient to remove the hasD encoded step as a limiting step. In summary, these results indicate that, with a proper balance between the synthesis pathways to UDP-GlcNAc and UDP-GlcUA, the hyaluronan molecular weight can be further increased and controlled.
In addition to the ratio between the two precursors, the importance of the ratio between precursor UDP-GlcUA and HA synthase also influences hyaluronan molecular weight. This was demonstrated for the heterologous host L. lactis, two plasmids were constructed containing either hasA or hasB from S. zooepidemicus with the inducible expression promoters NICE and lacA. Hyaluronan molecular weight increased significantly at hasA/hasB ratios below 2, indicating that higher UDP-GlcUA availability per HA synthase enhances hyaluronan molecular weight .
To conclude, production of hyaluronan by fermentation of streptococci strains is a mature technology, affording high molecular weight, highly pure polymers suitable for medical, pharmaceutical and cosmetic applications. Several tons per year of bacterial hyaluronan are currently produced for medical and cosmetic applications. Companies that produce hyaluronan through streptococcal fermentation are, for instance, Q-Med (Uppsala, Sweden), Lifecore Biomedical (Chaska, USA), and Genzyme (Cambridge, USA).
3.2.2. Hyaluronan from Recombinant Nonpathogenic Microorganisms
To avoid the risk of exotoxin contamination in hyaluronan products from pathogenic streptococci strains, safe organisms have been genetically engineered into hyaluronan producers, by introducing HA synthase enzymes from either streptococci or P. multocida. Using this approach, hyaluronan producing strains of Enterococcus faecalis , E. coli [7, 48, 96, 97], Bacillus subtilis , Agrobacterium sp. , and L. lactis [95, 100–102] were obtained and exploited for hyaluronan production. Heterologous expression of HA synthase (hasA gene in streptococci) was sufficient to induce production of hyaluronan. Since the hyaluronan biosynthesis has partially a common pathway with cell wall biosynthesis (Figure 3), production of hyaluronan by the host goes, however, on the expense of cell growth, due to the depletion of sugar precursors. Better hyaluronan producing heterologous strains with improved intracellular availability of sugar precursors were obtained by coexpression of the HA synthase hasA gene derived from S. equi or P. multocida with hasB homologue (UDP-glucose dehydrogenase) or hasB + hasC homologues (UDP-glucose dehydrogenase + UDP-glucose pyrophosphorylase) from E. coli. A recombinant E. coli strain obtained using this strategy produced 2 g L−1 hyaluronan, and the yield was increased to 3.8 g L−1 when the culture media was supplemented with glucosamine .
Using a similar strategy, namely the coexpression of the HA synthase hasA gene from P. multocida with hasB homologue (UDP-glucose dehydrogenase) from E. coli, into the food-grade microorganisms Agrobacterium sp.  and L. lactis , these strains were able to produce hyaluronan at levels up to 0.3 g L−1 for engineered Agrobacterium sp. and 0.65 g L−1 for the recombinant L. lactis. Although hyaluronan production yields were low, the hyaluronan production from these food-grade microorganisms has high potential for food and biomedical applications.
Without overexpression of hasB or an analog encoding for UDP-glucose dehydrogenase, UDP-GlcUA levels are often limiting in heterologous hosts [7, 97, 98, 101], whereas UDP-GlcNAc seems to be adequately available in the hosts since it is a main component for bacterial cell wall synthesis. Attempts to overexpress both synthetic pathways to UDP-GlcNAc and UDP-GlcUA in heterologous hosts have been so far unsuccessful, but overexpression of hasA, hasB, and hasC has led to considerable increases in hyaluronan synthesis varying between 200 and 800% depending on the host [96, 100].
A process for the production of ultrapure sodium hyaluronate by the fermentation of a novel, nonpathogenic recombinant strain of B. subtilis was developed by the biotech company Novozymes . A major advantage of using B. subtilis as host microorganism is that it is cultivable at large scale, does not produce exo- and endotoxins, and does not produce hyaluronidase. To build up the recombinant Bacillus strain that produces hyaluronan, expression constructs utilizing the hasA gene from S. equisimilis in combination with overexpression of one or more of the three native B. subtilis precursors genes—tuaD (hasB homologue, encoding UDP-glucose dehydrogenase), gtaB (hasC, encoding UDP-glucose pyrophosphorylase), and gcaD (hasD, encoding UDP-N-acetyl glucosamine pyrophosphorylase). The recombinant B. subtilis strain was able to produce up to 5 g L−1 of hyaluronan with a molecular weight of 1–1.2 million Da, when cultivated on a minimal medium based on sucrose at pH 7 and 37°C . The hyaluronan is secreted into the medium and is not cell-associated, which simplifies the downstream processing significantly, making the use of water-based solvents possible for hyaluronan recovery. The Bacillus hyaluronan shows very low levels of contaminants (i.e., proteins, nucleic acids, metal ions, and exo- and endotoxins) and thus has a high safety profile, including no risks of viral contamination or of transmission of animal spongiform encephalopathy.
As an alternative to prokaryotic HA production, hyaluronan can be produced by infecting green algae cells of the genus Chlorella with a virus [45, 104], although the reported yields were low (0.5–1 g L−1).
3.3. In Vitro Production of Hyaluronan Using Isolated HA Synthase
Synthesis of hyaluronan using isolated HA synthase becomes relevant when hyaluronan polymers of defined molecular weight and narrow polydispersity are needed. Isolated HA synthase is able to catalyze in vitro at well-defined conditions the same reaction as it catalyzes in vivo, namely, the synthesis of hyaluronan from the nucleotide sugars UDP-GlcNAc and UDP-GlcUA. Preparative enzymatic synthesis of hyaluronan using the crude membrane-bound HA synthase from S. pyogenes was demonstrated, although the yield was low, around 20% . The hyaluronan yield was increased to 90% when the enzymatic hyaluronan synthesis was coupled with in situ enzymatic regeneration of the sugar nucleotides using UDP and relatively inexpensive substrates, Glc-1-P and GlcNAc-1-P in a one-pot reaction. The average molecular weight of the synthetic hyaluronan was around 5.5 × 105 Da, corresponding to a degree of polymerization of 1500.
High molecular weight monodisperse hyaluronan polymers with up to 2.500 kDa (~12,000 sugar units) and polydispersity () of 1.01–1.20 were obtained by enzymatic polymerization using the recombinant P. multocida HA synthase, PmHAS, overexpressed in E. coli . PmHAS uses two separate glycosyl transferase sites to add GlcNAc and GlcUA monosaccharides to the nascent polysaccharide chain. Hyaluronan synthesis with PmHAS was achieved either by de novo synthesis from the two UDP-sugars precursors (1) and by elongation of an hyaluronan-like acceptor oligosaccharide chain by alternating, repetitive addition of the UDP-sugars as follows:
The control of the chain length and polydispersity of the hyaluronan polymer is determined by the intrinsic enzymological properties of the recombinant PmHAS, (i) the rate limiting step of the in vitro polymerization appears to be the chain initiation, and (ii) in vitro enzymatic polymerization is a fast nonprocessive reaction. Therefore, the concentration of the hyaluronan acceptor controls the size and the polydispersity of the hyaluronan polymer in the presence of a finite amount of UDP-sugar monomers . Using this synchronized, stoichiometrically-controlled enzymatic polymerization reaction, low molecular weight hyaluronan (~8 kDa) with narrow size distribution was synthesized. One important feature of the PmHAS is that chain elongation occurs at the nonreducing end of the growing chain and this makes the use of modified acceptors as substrates possible and consequently the synthesis of hyaluronan polymers with various end-moieties. The elongation of a hyaluronan tetrasaccharide labeled at the reducing end with the fluorophore 2-aminobenzoic acid using PmHAS and the quantitative formation of fluorescent hyaluronan oligomers and polymers was demonstrated [10, 107].
These studies have shown the high potential of the in vitro enzymatic synthesis of hyaluronan polymers and oligomers with low polydispersity, but for the large scale application further developments are needed. Technological bottlenecks that must be resolved are (a) production of robust enzymes for hyaluronan synthesis, (b) selective separation of the UDP byproduct from the reaction mixture, to prevent enzyme inactivation and to allow UDP recycling for the synthesis of UDP-sugar substrates, (c) development of efficient processes for the production of the hyaluronan-like template for elongation, and (d) the development of simple, low cost technologies for the synthesis of sugar nucleotide substrates starting from bulk carbohydrates. Since sugar nucleotides are expensive substrates their regeneration is a crucial step for the development of an economic process for the production of hyaluronan.
For in vitro production of hyaluronan the Class I HA synthases are less suitable due to the fact that they are integral membrane proteins. Research with these HA synthases is mostly performed on membrane fractions but this system is less suitable for larger scale production. An alternative could be the immobilization of the enzyme in the cell wall of for instance yeast. Production of various human oligosaccharides has shown to be feasible with yeast cells in which glycosyl transferases are expressed and anchored in the cell wall glucan .
A far more promising enzyme for in vitro production of hyaluronan is the P. multocida Class II HA synthase. This enzyme is not an integral membrane protein and the analysis of the subcellular location and enzyme activity has shown that a recombinant truncated version of the protein lacking a 216 carboxy terminal amino acids retained HA synthase activity but was located in the cytoplasm when expressed in E. coli . Furthermore, it was shown that two distinct transferase activities are located on the P. multocida HA synthase each of which can be inactivated by mutations in the DXD amino acid motif present in the active site while retaining the other transferase activity .
UDP-Recycling and Sugar Nucleotide Synthesis (Enzymatic Cascade, Bacterial Production). The general metabolic routes for incorporation of sugar units into glycosaminoglycans are their prior conversion into sugar nucleotides such as UDP-GlcA and UDP-GlcNAc for hyaluronan synthesis. The biosynthetic reactions are known as LeLoir pathways and these pathways can be different in microorganisms . For example, the pathways for the synthesis of UDP-GlcNAc in eukaryotes and prokaryotes are different. Production of sugar nucleotides needs also cofactor regeneration for preparative applications, because the cofactors are too expensive to be used as stoichiometric agents. Nowadays, several cofactors can be effectively regenerated using enzymes, for example, NAD+ by glutamate dehydrogenase with -ketoglutarate, or whole cell based methods, for example, Corynebacterium ammoniagenes that converts orotic acid into UTP [112–115].
4. Future Perspectives
Hyaluronan, with its exceptional properties and multiple and diverse applications, has proved to be an exceptional material for medical, pharmaceutical, and cosmetic applications. Tremendous developments have been achieved in the past decades in all hyaluronan-related fields, covering the whole chain from the production of hyaluronan polymers and oligomers, to the development of advanced materials for clinical applications. Latest accomplishments in hyaluronan production and in particular the elucidation of the biosynthetic pathways in hyaluronan producing microorganisms opens new premises for the further optimization of biotechnological process for hyaluronan production with safe hosts. Further understanding of the in vivo regulation of hyaluronan molecular weight will benefit the biotechnological production of defined hyaluronan products with narrow polydispersity. We believe that bacterial fermentation using nonpathogenic, safe heterologous hosts will become the main source of high molecular weight hyaluronan, and metabolic engineering will be used to improve and control molecular weight. Stimulated by the developments of production techniques and the growing knowledge on the biological function of hyaluronan, research to enhancing existing medical products and to validating new concepts in medical therapies will be set forth.
|BSE:||Bovine spongiform encephalopathy|
|HA synthase or HAS:||Hyaluronan synthase|
|:||Weight average molecular mass|
|:||Number average molecular mass|
|GMO:||Genetically modified organism.|
- P. L. DeAngelis, “Glycosaminoglycan polysaccharide biosynthesis and production: today and tomorrow,” Applied Microbiology and Biotechnology, vol. 94, no. 2, pp. 295–305, 2012.
- H. G. Garg and C. A. Hales, Chemistry and Biology of Hyaluronan, Elsevier, 2004.
- K. Meyer and J. W. Palmer, “The polysaccharde of the vitreous humor,” The Journal of Biological Chemistry, vol. 107, no. 3, pp. 629–634, 1934.
- B. Weissmann and K. Meyer, “The structure of hyalobiuronic acid and of hyaluronic acid from umbilical cord,” Journal of the American Chemical Society, vol. 76, no. 7, pp. 1753–1757, 1954.
- E. A. Balazs, “Ultrapure hyaluronic acid and the use thereof,” U.S. Patent, US4141973, 1979.
- P. L. DeAngelis, J. Papaconstantinou, and P. H. Weigel, “Molecular cloning, identification, and sequence of the hyaluronan synthase gene from group A Streptococcus pyogenes,” The Journal of Biological Chemistry, vol. 268, no. 26, pp. 19181–19184, 1993.
- P. L. DeAngelis, J. Papaconstantinou, and P. H. Weigel, “Isolation of a Streptococcus pyogenes gene locus that directs hyaluronan biosynthesis in acapsular mutants and in heterologous bacteria,” The Journal of Biological Chemistry, vol. 268, no. 20, pp. 14568–14571, 1993.
- G. Blatter and J. C. Jacquinet, “The use of 2-deoxy-2-trichloroacetamido-D-glucopyranose derivatives in syntheses of hyaluronic acid-related tetra-, hexa-, and octa-saccharides having a methyl β-D-glucopyranosiduronic acid at the reducing end,” Carbohydrate Research, vol. 288, pp. 109–125, 1996.
- P. L. DeAngelis, L. C. Oatman, and D. F. Gay, “Rapid chemoenzymatic synthesis of monodisperse hyaluronan oligosaccharides with immobilized enzyme reactors,” The Journal of Biological Chemistry, vol. 278, no. 37, pp. 35199–35203, 2003.
- F. K. Kooy, Enzymatic Production of Hyaluronan Oligo- and Polysaccharides, Wageningen University, Wageningen, The Netherlands, 2010.
- B. Porsch, R. Laga, and C. Konak, “Batch and size-exclusion chromatographic characterization of ultra-high molar mass sodium hyaluronate containing low amounts of strongly scattering impurities by dual low angle light scattering/refractometric detection,” Journal of Liquid Chromatography and Related Technologies, vol. 31, no. 20, pp. 3077–3093, 2008.
- A. Shiedlin, R. Bigelow, W. Christopher et al., “Evaluation of hyaluronan from different sources: streptococcus zooepidemicus, rooster comb, bovine vitreous, and human umbilical cord,” Biomacromolecules, vol. 5, no. 6, pp. 2122–2127, 2004.
- R. Mendichi and L. Soltes, “Hyaluronan molecular weight and polydispersity in some commercial intra-articular injectable preparations and in synovial fluid,” Inflammation Research, vol. 51, no. 3, pp. 115–116, 2002.
- R. Stern, “Devising a pathway for hyaluronan catabolism: are we there yet?” Glycobiology, vol. 13, no. 12, pp. 105R–115R, 2003.
- M. Erickson and R. Stern, “Chain gangs: new aspects of hyaluronan metabolism,” Biochemistry Research International, vol. 2012, Article ID 893947, 9 pages, 2012.
- T. C. Laurent and J. R. E. Fraser, “Hyaluronan,” The FASEB Journal, vol. 6, no. 7, pp. 2397–2404, 1992.
- P. L. DeAngelis, “Hyaluronan synthases: Fascinating glycosyltransferases from vertebrates, bacterial pathogens, and algal viruses,” Cellular and Molecular Life Sciences, vol. 56, no. 7-8, pp. 670–682, 1999.
- T. E. Hardingham and H. Muir, “The specific interaction of hyaluronic acid with cartilage proteoglycans,” Biochimica et Biophysica Acta, vol. 279, no. 2, pp. 401–405, 1972.
- V. C. Hascall, “Hyaluronan, a common thread,” Glycoconjugate Journal, vol. 17, no. 7–9, pp. 607–616, 2000.
- N. Afratis, C. Gialeli, D. Nikitovic, et al., “Glycosaminoglycans: key players in cancer cell biology and treatment,” FEBS Journal, vol. 279, no. 7, pp. 1177–1197, 2012.
- C. Schiraldi, A. La Gatta, and M. De Rosa, “Biotechnological production and application of hyaluronan,” in Biopolymers, M. Elnashar, Ed., pp. 387–412, InTech, Rijeka, Croatia, 2010.
- F. Freitas, V. D. Alves, and M. A. M. Reis, “Advances in bacterial exopolysaccharides: from production to biotechnological applications,” Trends in Biotechnology, vol. 29, no. 8, pp. 388–398, 2011.
- B. D. Ulery, L. S. Nair, and C. T. Laurencin, “Biomedical applications of biodegradable polymers,” Journal of Polymer Science B, vol. 49, no. 12, pp. 832–864, 2011.
- R. Stern, A. A. Asari, and K. N. Sugahara, “Hyaluronan fragments: an information-rich system,” European Journal of Cell Biology, vol. 85, no. 8, pp. 699–715, 2006.
- B. F. Chong, L. M. Blank, R. Mclaughlin, and L. K. Nielsen, “Microbial hyaluronic acid production,” Applied Microbiology and Biotechnology, vol. 66, no. 4, pp. 341–351, 2005.
- S. Ghatak, S. Misra, and B. P. Toole, “Hyaluronan oligosaccharides inhibit anchorage-independent growth of tumor cells by suppressing the phosphoinositide 3-kinase/Akt cell survival pathway,” The Journal of Biological Chemistry, vol. 277, no. 41, pp. 38013–38020, 2002.
- J. Y. Lee and A. P. Spicer, “Hyaluronan: a multifunctional, megaDalton, stealth molecule,” Current Opinion in Cell Biology, vol. 12, no. 5, pp. 581–586, 2000.
- P. L. DeAngelis and P. H. Weigel, “Immunochemical confirmation of the primary structure of streptococcal hyaluronan synthase and synthesis of high molecular weight product by the recombinant enzyme,” Biochemistry, vol. 33, no. 31, pp. 9033–9039, 1994.
- P. Prehm, “Hyaluronate is synthesized at plasma membranes,” Biochemical Journal, vol. 220, no. 2, pp. 597–600, 1984.
- A. A. E. Chavaroche, L. A. M. van den Broek, and G. Eggink, “Production methods for heparosan, a precursor of heparin and heparan sulfate,” Carbohydrate Polymers, vol. 93, no. 1, pp. 38–47, 2013.
- N. Itano, “Hyaluronan biosynthesis: a multifaceted process,” Connective Tissue, vol. 33, no. 3, pp. 221–226, 2001.
- C. A. de la Motte and J. A. Drazba, “Viewing hyaluronan: imaging contributes to imagining new roles for this amazing matrix polymer,” Journal of Histochemistry and Cytochemistry, vol. 59, no. 3, pp. 252–257, 2011.
- N. Itano and K. Kimata, “Molecular cloning of human hyaluronan synthase,” Biochemical and Biophysical Research Communications, vol. 222, no. 3, pp. 816–820, 1996.
- A. P. Spicer, M. L. Augustine, and J. A. McDonald, “Molecular cloning and characterization of a putative mouse hyaluronan synthase,” The Journal of Biological Chemistry, vol. 271, no. 38, pp. 23400–23406, 1996.
- N. Itano, T. Sawai, M. Yoshida et al., “Three isoforms of mammalian hyaluronan synthases have distinct enzymatic properties,” The Journal of Biological Chemistry, vol. 274, no. 35, pp. 25085–25092, 1999.
- P. Heldin, “Molecular mechanisms that regulate hyaluronan synthesis,” Gene Therapy and Molecular Biology, vol. 3, pp. 465–474, 1999.
- A. Jacobson, J. Brinck, M. J. Briskin, A. P. Spicer, and P. Heldin, “Expression of human hyaluronan syntheses in response to external stimuli,” Biochemical Journal, vol. 348, no. 1, pp. 29–35, 2000.
- B. A. Dougherty and I. Van de Rijn, “Molecular characterization of hasB from an operon required for hyaluronic acid synthesis in group A streptococci. Demonstration of UDP-glucose dehydrogenase activity,” The Journal of Biological Chemistry, vol. 268, no. 10, pp. 7118–7124, 1993.
- B. A. Dougherty and I. Van de Rijn, “Molecular characterization of hasA from an operon required for hyaluronic acid synthesis in group A streptococci,” The Journal of Biological Chemistry, vol. 269, no. 1, pp. 169–175, 1994.
- D. L. Crater, B. A. Dougherty, and I. Van de Rijn, “Molecular characterization of hasC from an operon required for hyaluronic acid synthesis in group A streptococci. Demonstration of UDP-glucose pyrophosphorylase activity,” The Journal of Biological Chemistry, vol. 270, no. 48, pp. 28676–28680, 1995.
- A. Markovitz, J. A. Cifonelli, and A. Dorfman, “The biosynthesis of hyaluronic acid by group A Streptococcus. VI. Biosynthesis from uridine nucleotides in cell-free extracts,” The Journal of Biological Chemistry, vol. 234, pp. 2343–2350, 1959.
- K. Kumari and P. H. Weigel, “Molecular cloning, expression, and characterization of the authentic hyaluronan synthase from Group C Streptococcus equisimilis,” The Journal of Biological Chemistry, vol. 272, no. 51, pp. 32539–32546, 1997.
- P. L. DeAngelis and A. M. Achyuthan, “Yeast-derived recombinant DG42 protein of Xenopus can synthesize hyaluronan in vitro,” The Journal of Biological Chemistry, vol. 271, no. 39, pp. 23657–23660, 1996.
- P. H. Weigel, V. C. Hascall, and M. Tammi, “Hyaluronan synthases,” The Journal of Biological Chemistry, vol. 272, no. 22, pp. 13997–14000, 1997.
- P. L. DeAngelis, W. Jing, M. V. Graves, D. E. Burbank, and J. L. Van Etten, “Hyaluronan synthase of chlorella virus PBCV-1,” Science, vol. 278, no. 5344, pp. 1800–1803, 1997.
- P. M. Coutinho, E. Deleury, G. J. Davies, and B. Henrissat, “An evolving hierarchical family classification for glycosyltransferases,” Journal of Molecular Biology, vol. 328, no. 2, pp. 307–317, 2003.
- A. Jong, C. H. Wu, H. M. Chen et al., “Identification and characterization of CPS1 as a hyaluronic acid synthase contributing to the pathogenesis of Cryptococcus neoformans infection,” Eukaryotic Cell, vol. 6, no. 8, pp. 1486–1496, 2007.
- P. L. DeAngelis, W. Jing, R. R. Drake, and A. M. Achyuthan, “Identification and molecular cloning of a unique hyaluronan synthase from Pasteurella multocida,” The Journal of Biological Chemistry, vol. 273, no. 14, pp. 8454–8458, 1998.
- P. H. Weigel and P. L. DeAngelis, “Hyaluronan synthases: a decade-plus of novel glycosyltransferases,” The Journal of Biological Chemistry, vol. 282, no. 51, pp. 36777–36781, 2007.
- S. Bodevin-Authelet, M. Kusche-Gullberg, P. E. Pummill, P. L. DeAngelis, and U. Lindahl, “Biosynthesis of hyaluronan: direction of chain elongation,” The Journal of Biological Chemistry, vol. 280, no. 10, pp. 8813–8818, 2005.
- P. E. Pummill, T. A. Kane, E. S. Kempner, and P. L. DeAngelis, “The functional molecular mass of the Pasteurella hyaluronan synthase is a monomer,” Biochimica et Biophysica Acta, vol. 1770, no. 2, pp. 286–290, 2007.
- P. L. DeAngelis, “Microbial glycosaminoglycan glycosyltransferases,” Glycobiology, vol. 12, no. 1, pp. 9R–16R, 2002.
- K. Rilla, H. Siiskonen, A. P. Spicer, J. M. T. Hyttinen, M. I. Tammi, and R. H. Tammi, “Plasma membrane residence of hyaluronan synthase is coupled to its enzymatic activity,” The Journal of Biological Chemistry, vol. 280, no. 36, pp. 31890–31897, 2005.
- M. Nardini, M. Ori, D. Vigetti, R. Gornati, I. Nardi, and R. Perris, “Regulated gene expression of hyaluronan synthases during Xenopus laevis development,” Gene Expression Patterns, vol. 4, no. 3, pp. 303–308, 2004.
- J. Y. L. Tien and A. P. Spicer, “Three vertebrate hyaluronan synthases are expressed during mouse development in distinct spatial and temporal patterns,” Developmental Dynamics, vol. 233, no. 1, pp. 130–141, 2005.
- M. Suzuki, T. Asplund, H. Yamashita, C. H. Heldin, and P. Heldin, “Stimulation of hyaluronan biosynthesis by platelet-derived growth factor-BB and transforming growth factor-β1 involves activation of protein kinase C,” Biochemical Journal, vol. 307, no. 3, pp. 817–821, 1995.
- H. Chao and A. P. Spicer, “Natural antisense mRNAs to hyaluronan synthase 2 inhibit hyaluronan biosynthesis and cell proliferation,” The Journal of Biological Chemistry, vol. 280, no. 30, pp. 27513–27522, 2005.
- D. Vigetti, A. Genasetti, E. Karousou et al., “Modulation of hyaluronan synthase activity in cellular membrane fractions,” The Journal of Biological Chemistry, vol. 284, no. 44, pp. 30684–30694, 2009.
- L. M. Blank, P. Hugenholtz, and L. K. Nielsen, “Evolution of the hyaluronic acid synthesis (has) operon in Streptococcus zooepidemicus and other pathogenic streptococci,” Journal of Molecular Evolution, vol. 67, no. 1, pp. 13–22, 2008.
- W. Y. Chen, E. Marcellin, J. Hung, and L. K. Nielsen, “Hyaluronan molecular weight is controlled by UDP-N-acetylglucosamine concentration in Streptococcus zooepidemicus,” The Journal of Biological Chemistry, vol. 284, no. 27, pp. 18007–18014, 2009.
- L. Soltes, R. Mendichi, D. Lath, M. Mach, and D. Bakoš, “Molecular characteristics of some commercial high-molecular-weight hyaluronans,” Biomedical Chromatography, vol. 16, no. 7, pp. 459–462, 2002.
- P. S. Harmon, E. P. Maziarz, and X. M. Liu, “Detailed characterization of hyaluronan using aqueous size exclusion chromatography with triple detection and multiangle light scattering detection,” Journal of Biomedical Materials Research B, vol. 100, no. 7, pp. 1955–1960, 2012.
- E. U. Ignatova and A. N. Gurov, “Principles of extraction and purification of hyaluronic acid,” Khimiko-Farmatsevticheskii Zhurnal, vol. 24, no. 3, pp. 42–46, 1990.
- I. Amagai, Y. Tashiro, and H. Ogawa, “Improvement of the extraction procedure for hyaluronan from fish eyeball and the molecular characterization,” Fisheries Science, vol. 75, no. 3, pp. 805–810, 2009.
- M. O'Regan, I. Martini, F. Crescenzi, C. De Luca, and M. Lansing, “Molecular mechanisms and genetics of hyaluronan biosynthesis,” International Journal of Biological Macromolecules, vol. 16, no. 6, pp. 283–286, 1994.
- G. Kogan, L. Šoltés, R. Stern, and P. Gemeiner, “Hyaluronic acid: a natural biopolymer with a broad range of biomedical and industrial applications,” Biotechnology Letters, vol. 29, no. 1, pp. 17–25, 2007.
- J. C. Thonard, S. A. Migliore, and R. Blustein, “Isolation of hyaluronic acid from broth cultures of Streptococci,” The Journal of Biological Chemistry, vol. 239, pp. 726–728, 1964.
- F. E. Kendall, M. Heidelberger, and M. H. Dawson, “A serologically inactive polysaccharide elaborated by mocoid strains of group A hemolytic Streptococcus,” The Journal of Biological Chemistry, vol. 118, no. 1, pp. 61–69, 1937.
- B. Holmstrom and J. Ricica, “Production of hyaluronic acid by a Streptococcal strain in batch culture,” Applied Environmental Microbiology, vol. 15, no. 6, pp. 1409–1413, 1967.
- J. H. Kim, S. J. Yoo, D. K. Oh et al., “Selection of a Streptococcus equi mutant and optimization of culture conditions for the production of high molecular weight hyaluronic acid,” Enzyme and Microbial Technology, vol. 19, no. 6, pp. 440–445, 1996.
- N. Izawa, T. Hanamizu, R. Iizuka et al., “Streptococcus thermophilus produces exopolysaccharides including hyaluronic acid,” Journal of Bioscience and Bioengineering, vol. 107, no. 2, pp. 119–123, 2009.
- N. Izawa, M. Serata, T. Sone, T. Omasa, and H. Ohtake, “Hyaluronic acid production by recombinant Streptococcus thermophilus,” Journal of Bioscience and Bioengineering, vol. 111, no. 6, pp. 665–670, 2011.
- H. J. Gao, G. C. Du, and J. Chen, “Analysis of metabolic fluxes for hyaluronic acid (HA) production by Streptococcus zooepidemicus,” World Journal of Microbiology and Biotechnology, vol. 22, no. 4, pp. 399–408, 2006.
- X. J. Duan, H. X. Niu, W. S. Tan, and X. Zhang, “Mechanism analysis of effect of oxygen on molecular weight of hyaluronic acid produced by Streptococcus zooepidemicus,” Journal of Microbiology and Biotechnology, vol. 19, no. 3, pp. 299–306, 2009.
- J. Zhang, X. Ding, L. Yang, and Z. Kong, “A serum-free medium for colony growth and hyaluronic acid production by Streptococcus zooepidemicus NJUST01,” Applied Microbiology and Biotechnology, vol. 72, no. 1, pp. 168–172, 2006.
- J. H. Im, J. M. Song, J. H. Kang, and D. J. Kang, “Optimization of medium components for high-molecular-weight hyaluronic acid production by Streptococcus sp. ID9102 via a statistical approach,” Journal of Industrial Microbiology and Biotechnology, vol. 36, no. 11, pp. 1337–1344, 2009.
- D. C. Armstrong, M. J. Cooney, and M. R. Johns, “Growth and amino acid requirements of hyaluronic-acid producing Streptococcus zooepidemicus,” Applied Microbiology and Biotechnology, vol. 47, no. 3, pp. 309–312, 1997.
- M. J. Cooney, L. T. Goh, P. L. Lee, and M. R. Johns, “Structured model-based analysis and control of the hyaluronic acid fermentation by Streptococcus zooepidemicus: physiological implications of glucose and complex-nitrogen-limited growth,” Biotechnology Progress, vol. 15, no. 5, pp. 898–910, 1999.
- W. C. Huang, S. J. Chen, and T. L. Chen, “The role of dissolved oxygen and function of agitation in hyaluronic acid fermentation,” Biochemical Engineering Journal, vol. 32, no. 3, pp. 239–243, 2006.
- B. F. Chong and L. K. Nielsen, “Aerobic cultivation of Streptococcus zooepidemicus and the role of NADH oxidase,” Biochemical Engineering Journal, vol. 16, no. 2, pp. 153–162, 2003.
- B. F. Chong and L. K. Nielsen, “Amplifying the cellular reduction potential of Streptococcus zooepidemicus,” Journal of Biotechnology, vol. 100, no. 1, pp. 33–41, 2003.
- T. F. Wu, W. C. Huang, Y. C. Chen, Y. G. Tsay, and C. S. Chang, “Proteomic investigation of the impact of oxygen on the protein profiles of hyaluronic acid-producing Streptococcus zooepidemicus,” Proteomics, vol. 9, no. 19, pp. 4507–4518, 2009.
- M. R. Johns, L. T. Goh, and A. Oeggerli, “Effect of pH, agitation and aeration on hyaluronic acid production by Streptococcus zooepidemicus,” Biotechnology Letters, vol. 16, no. 5, pp. 507–512, 1994.
- S. Hasegawa, M. Nagatsuru, M. Shibutani, S. Yamamoto, and S. Hasebe, “Productivity of concentrated hyaluronic acid using a Maxblend (R) fermentor,” Journal of Bioscience and Bioengineering, vol. 88, no. 1, pp. 68–71, 1999.
- X. Zhang, X. J. Duan, and W. S. Tan, “Mechanism for the effect of agitation on the molecular weight of hyaluronic acid produced by Streptococcus zooepidemicus,” Food Chemistry, vol. 119, no. 4, pp. 1643–1646, 2010.
- M. Cazzola, F. O'regan, and V. Corsa, “Culture medium and process for the preparation of high molecular weight hyaluronic acid,” Fidia Advanced Biopolymers S.R.L., 2003.
- I. Van De Rijn, “Streptococcal hyaluronic acid: Proposed mechanisms of degradation and loss of synthesis during stationary phase,” Journal of Bacteriology, vol. 156, no. 3, pp. 1059–1065, 1983.
- A. Mausolf, J. Jungmann, H. Robenek, and P. Prehm, “Shedding of hyaluronate synthase from streptococci,” Biochemical Journal, vol. 267, no. 1, pp. 191–196, 1990.
- D. C. Ellwood, C. G. T. Evans, G. M. Dunn, et al., “Production of hyaluronic acid,” Fermentech Medical Limited, 1996.
- W. C. Huang, S. J. Chen, and T. L. Chen, “Production of hyaluronic acid by repeated batch fermentation,” Biochemical Engineering Journal, vol. 40, no. 3, pp. 460–464, 2008.
- L. M. Blank, R. L. McLaughlin, and L. K. Nielsen, “Stable production of hyaluronic acid in streptococcus zooepidemicus chemostats operated at high dilution rate,” Biotechnology and Bioengineering, vol. 90, no. 6, pp. 685–693, 2005.
- H. Y. Han, S. H. Jang, E. C. Kim, et al., “Microorganism producing hyaluronic acid and purification method of hyaluronic acid,” p. 26, 2004.
- S. Stahl, “Methods and means for the production of hyaluronic acid,” US6090596, 2000.
- E. Marcellin, W. Y. Chen, and L. K. Nielsen, “Understanding plasmid effect on hyaluronic acid molecular weight produced by Streptococcus equi subsp. zooepidemicus,” Metabolic Engineering, vol. 12, no. 1, pp. 62–69, 2010.
- J. Z. Sheng, P. X. Ling, X. Q. Zhu et al., “Use of induction promoters to regulate hyaluronan synthase and UDP-glucose-6-dehydrogenase of Streptococcus zooepidemicus expression in Lactococcus lactis: a case study of the regulation mechanism of hyaluronic acid polymer,” Journal of Applied Microbiology, vol. 107, no. 1, pp. 136–144, 2009.
- H. Yu and G. Stephanopoulos, “Metabolic engineering of Escherichia coli for biosynthesis of hyaluronic acid,” Metabolic Engineering, vol. 10, no. 1, pp. 24–32, 2008.
- Z. Mao, H. D. Shin, and R. Chen, “A recombinant E. coli bioprocess for hyaluronan synthesis,” Applied Microbiology and Biotechnology, vol. 84, no. 1, pp. 63–69, 2009.
- B. Widner, R. Behr, S. Von Dollen et al., “Hyaluronic acid production in Bacillus subtilis,” Applied and Environmental Microbiology, vol. 71, no. 7, pp. 3747–3752, 2005.
- Z. Mao and R. R. Chen, “Recombinant synthesis of hyaluronan by Agrobacterium sp,” Biotechnology Progress, vol. 23, no. 5, pp. 1038–1042, 2007.
- S. B. Prasad, G. Jayaraman, and K. B. Ramachandran, “Hyaluronic acid production is enhanced by the additional co-expression of UDP-glucose pyrophosphorylase in Lactococcus lactis,” Applied Microbiology and Biotechnology, vol. 86, no. 1, pp. 273–283, 2010.
- L. J. Chien and C. K. Lee, “Hyaluronic acid production by recombinant Lactococcus lactis,” Applied Microbiology and Biotechnology, vol. 77, no. 2, pp. 339–346, 2007.
- S. B. Prasad, K. B. Ramachandran, and G. Jayaraman, “Transcription analysis of hyaluronan biosynthesis genes in Streptococcus zooepidemicus and metabolically engineered Lactococcus lactis,” Applied Microbiology and Biotechnology, vol. 94, no. 6, pp. 1593–1607, 2012.
- A. Sloma, et al., “Recombinant expression of bacterial hyaluronan synthase operon genes in Bacillus and hyaluronic acid production,” p. 218, 2003.
- M. V. Graves, D. E. Burbank, R. Roth, J. Heuser, P. L. Deangelis, and J. L. Van Etten, “Hyaluronan synthesis in virus PBCV-1-infected chlorella-like green algae,” Virology, vol. 257, no. 1, pp. 15–23, 1999.
- C. De Luca, M. Lansing, I. Martini et al., “Enzymatic synthesis of hyaluronic acid with regeneration of sugar nucleotides,” Journal of the American Chemical Society, vol. 117, no. 21, pp. 5869–5870, 1995.
- P. L. DeAngelis, “Monodisperse hyaluronan polymers: synthesis and potential applications,” Current Pharmaceutical Biotechnology, vol. 9, no. 4, pp. 246–248, 2008.
- F. K. Kooy, M. Ma, H. H. Beeftink, G. Eggink, J. Tramper, and C. G. Boeriu, “Quantification and characterization of enzymatically produced hyaluronan with fluorophore-assisted carbohydrate electrophoresis,” Analytical Biochemistry, vol. 384, no. 2, pp. 329–336, 2009.
- Y. I. Shimma, F. Saito, F. Oosawa, and Y. Jigami, “Construction of a library of human glycosyltransferases immobilized in the cell wall of Saccharomyces cerevisiae,” Applied and Environmental Microbiology, vol. 72, no. 11, pp. 7003–7012, 2006.
- W. Jing and P. L. De Angelis, “Dissection of the two transferase activities of the Pasteurella multocida hyaluronan synthase: two active sites exist in one polypeptide,” Glycobiology, vol. 10, no. 9, pp. 883–889, 2000.
- W. Jing and P. L. DeAngelis, “Analysis of the two active sites of the hyaluronan synthase and the chondroitin synthase of Pasteurella multocida,” Glycobiology, vol. 13, no. 10, pp. 661–671, 2003.
- S. Milewski, I. Gabriel, and J. Olchowy, “Enzymes of UDP-GlcNAc biosynthesis in yeast,” Yeast, vol. 23, no. 1, pp. 1–14, 2006.
- H. Zhao and W. A. Van Der Donk, “Regeneration of cofactors for use in biocatalysis,” Current Opinion in Biotechnology, vol. 14, no. 6, pp. 583–589, 2003.
- A. Ruffing and R. R. Chen, “Metabolic engineering of microbes for oligosaccharide and polysaccharide synthesis,” Microbial Cell Factories, vol. 5, p. 25, 2006.
- W. Liu and P. Wang, “Cofactor regeneration for sustainable enzymatic biosynthesis,” Biotechnology Advances, vol. 25, no. 4, pp. 369–384, 2007.
- C. A. G. M. Weijers, M. C. R. Franssen, and G. M. Visser, “Glycosyltransferase-catalyzed synthesis of bioactive oligosaccharides,” Biotechnology Advances, vol. 26, no. 5, pp. 436–456, 2008.