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Ruchi Mutreja, Debasish Das, Dinesh Goyal, Arun Goyal, "Bioconversion of Agricultural Waste to Ethanol by SSF Using Recombinant Cellulase from Clostridium thermocellum", Enzyme Research, vol. 2011, Article ID 340279, 6 pages, 2011. https://doi.org/10.4061/2011/340279
Bioconversion of Agricultural Waste to Ethanol by SSF Using Recombinant Cellulase from Clostridium thermocellum
The effect of different pretreatment methods, temperature, and enzyme concentration on ethanol production from 8 lignocellulosic agrowaste by simultaneous saccharification and fermentation (SSF) using recombinant cellulase and Saccharomyces cerevisiae were studied. Recombinant cellulase was isolated from E. coli BL21 cells transformed with CtLic26A-Cel5-CBM11 full-length gene from Clostridium thermocellum and produced in both batch and fed-batch processes. The maximum cell OD and specific activity in batch mode were 1.6 and 1.91 U/mg, respectively, whereas in the fed-batch mode, maximum cell OD and specific activity were 3.8 and 3.5 U/mg, respectively, displaying a 2-fold increase. Eight substrates, Syzygium cumini (jamun), Azadirachta indica (neem), Saracens indica (asoka), bambusa dendrocalmus (bamboo), Populas nigra (poplar), Achnatherum hymenoides (wild grass), Eucalyptus marginata (eucalyptus), and Mangifera indica (mango), were subjected to SSF. Of three pretreatments, acid, alkali, and steam explosion, acid pretreatment Syzygium cumini (Jamun) at 30°C gave maximum ethanol yield of 1.42 g/L.
The depleting fossil fuel resources has forced mankind to depend on the renewable energy sources, and bioethanol is one of them. Ethanol is used as a fuel, as it offers many advantages such as it has lower thermal energy content (about 45% less per gallon than diesel), low price, and with comparatively less emissions than gasoline or diesel. Ethanol has a high octane number (99) than petrol (80–100) as a result of which preignition does not occur when ethanol is used. Hence, ethanol is used widely as a competitive fuel additive with gasoline and rarely in pure form [1, 2]. Currently, biofuels such as bioethanol, biodiesel, biohydrogen, and methane from lignocellulosic biomass are produced from agrowastes rather than from energy crops, as they compete with food crops. The agricultural wastes are abundant and have disposal problem. An alternative is to utilize the lignocellulosic biomass so that the competition between food and fuel can be minimized . Lignocellulosic biomass in the form of plant materials such as grass, wood, and crop residues offers the possibility of a renewable and relatively greenhouse-gas favoring source of sugars that can be converted to ethanol. The potential for using lignocellulosic materials in bioethanol production is well recognized. However, hydrolyzing lignocelluloses to fermentable reducing sugars is still a challenge, because it has a strong crystalline structure and is usually surrounded by lignin, which reduces accessibility to hydrolytic enzyme . The pretreatment of lignocellulosic biomass results in substantial breakdown of the lignocellulosic structure, hydrolysis of the hemicellulosic fraction, depolymerization of the lignin components, and defibration. Different types of pretreatment methods are used such as acid, alkali, steam explosion, and ozonolysis . The accessibility of cellulose components to the enzymes can be greatly enhanced by using an effective pretreatment strategy .
Ethanol produced from lignocellulosic biomass using separate hydrolysis and fermentation had problems as the higher concentration of reducing sugars inhibited the growth of yeast . Moreover, two fermentors were required, one for hydrolysis and the other for fermentation; therefore, the process was not cost effective . The solution to above problems was provided by simultaneous saccharification and fermentation (SSF) in which reducing sugars formed by hydrolysis are simultaneously converted into ethanol by yeast fermentation . But the problem with SSF is the optimum temperature, since for enzyme hydrolysis, optimum temperature is 50°C and for fermentation by yeast is 30°C, so compromised condition has to be taken for ethanol production by SSF. Extensive work has been done on ethanol production by SSF from lignocellulosic waste (LCW), such as forestry wastes, bagasse, corn stalk and cobs, wheat straw, grasses, and rice straw, using cellulase from natural and commercial sources [7–9], but there is no literature available on the use of recombinant cellulases for enzyme hydrolysis during saccharification. Jamun, eucalyptus, neem, mango, asoka, bamboo, wild grass, and poplar are among the most common crops found in north India. Also, no literature is available on the use of above-mentioned substrates for ethanol production. Due to their abundance, there is a great deal of interest in utilizing LCW for production and recovery of many value-added products such as ethanol [8–10]. Besides the type of pretreatment method, other parameters such as enzyme activity and enzyme concentration, temperature, and pH affect the ethanol yield from the biomass. The present study aims at increasing the enzymatic activity of recombinant cellulase by using fed-batch strategy and increasing the ethanol yield by applying best pretreatment strategy and optimizing the enzyme concentration and temperature for SSF using S. cerevisiae.
2. Materials and Methods
2.1. Chemicals and Reagents
Carboxy methyl cellulose was purchased from Sigma Aldrich, USA. Sodium acetate, acetic acid, ampicillin, components of LB and GYE medium, and other reagents were purchased from HiMedia Pvt. Ltd., India.
2.2. Microorganisms and Medium
Saccahromyces cereviseae used for the production of ethanol by SSF was procured from Microbial Type Culture Collection (MTCC), Chandigarh, India. It was maintained in agar slants by storing at 4°C and was inoculated in GYE medium which was sterilized by autoclaving at 121°C for 20 min and was then incubated at 30°C, 120 rpm. 1 mL of actively growing culture was transferred to 100 mL of culture medium. Recombinant E. coli BL21 cells transformed with plasmid containing CtLic26A-Cel5-CBM11 gene from Clostridium thermocellum inserted in an expression vector pET21a was used as a source for cellulase enzyme and was developed and maintained by the group . The cells were maintained as glycerol stock at −80°C. 200 μL of the glycerol stock was transferred to 5 mL of LB medium containing 100 μg/mL ampicillin and incubated at 37°C, 180 rpm for 16 h. 1 mL of this culture was inoculated to 100 mL of LB medium containing 100 μg/mL ampicillin and incubated at 37°C, 180 rpm for 12 h.
2.3. Processing of Agrowaste Substrates
Eight different substrates were subjected to SSF study each having different cellulosic, hemicellulosic, and lignin content, namely, Syzygium cumini (jamun), Azadirachta indica (neem), Saracens indica (asoka), Bambusa dendrocalmus (bamboo), Populas nigra (poplar), Achnatherum hymenoides (wild grass), Eucalyptus marginata (eucalyptus), and Mangifera indica (mango). Leaves of jamun, mango, neem, eucalyptus, poplar, asoka, wild grass, and bamboo were supplied by Science, and Technology Entrepreneur's Park (STEP), Thaper University, Patiala, Punjab, India. Prior to pretreatment, the dry agro biomass was washed three times with water in order to remove unwanted dust particles and then air-dried at room temperature. The dry biomass was then grinded in a grinder and sieved to a mesh size of 1 mm.
2.4. Recombinant Cellulase Production by Batch and Fed-Batch Process
For batch mode process, the E. coli BL-21 cells containing the recombinant cellulase were grown in 500 mL flask containing 250 mL of LB medium having 100 μg/mL ampicillin . The dynamic profile of enzyme activity and growth was monitored by collecting sample at every 1 h. For induction of cellulase expression, IPTG (1 mM final concentration) was added to the broth when the cell OD at 600 nm reached 0.6. In order to enhance the enzymatic activity, the cells were grown in fed-batch mode. In the fed-batch strategy, the initial step remained the same as that for batch mode, and 245 mL of medium was withdrawn when the cells reached late log phase or early stationary phase. This cell mass from 245 mL were removed by centrifugation and processed for the isolation of crude enzyme, and the same volume of fresh medium was added and further incubated till stationary phase was reached. The same procedure was followed in consecutive four batches, where induced cells were used as inoculum. Fed-batch cultivation mode was used in order to produce maximum amount of cellulase and growth of recombinant E. coli. The enzyme was isolated by sonication of cells from both batch and fed-batch strategies.
2.5. Pretreatment of Substrates
The physically pretreated substrates were further subjected to pretreatment by steam explosion, alkali pretreatment, and acid pretreatment.
2.5.1. Steam Explosion
Steam explosion of raw material was carried out at flask level. 1 g of raw material was taken in the 100 mL flask, and then, each of the powdered substrate was subjected to sudden steam depressurization in an autoclave (15 psi, 15 min, and 121°C) by fully opening the steam exhaust valve with the objective of obtaining the maximum quantity of fermentable sugars using least pretreatment time .
2.5.2. Alkali Pretreatment
Each of the powdered substrates was assessed using the combined treatment with dilute alkali and autoclaving technique. 1 g of each substrate in 20 mL of 0.5 M NaOH solution was autoclaved at 115°C for 10 min . After cooling, the residues were washed with sodium acetate buffer (0.02 M, pH 4.3) and distilled water, subsequently, followed by centrifugation (10,000 g, 10 min) till the pH became neutral. The residues are dried in an oven at 70°C for 24 h.
2.5.3. Acid Pretreatment
Each of the powdered substrates was assessed using the combined treatment of acid, alkali and, autoclaving techniques. 1 g of each substrate in 10 mL of 1% H2SO4  was autoclaved at 121°C for 15 min After cooling, the supernatant was decanted, and the residues were washed with 1% NaOH and then with distilled water, alternatively, by first vortexing and then centrifugation at 10,000 g for 10 min till the pH become neutral, then the residues were dried in an oven at 70°C for 24 h.
2.6. Simultaneous Saccharification and Fermentation (SSF)
SSF experiments were carried out in 250 mL Erlenmeyer flasks, each containing 100 mL of fermentation medium in 0.02 M sodium acetate buffer (pH 4.3) at 30°C on a rotary incubator shaker at 120 rpm for 72 h and at 1% (w/v) pretreated material concentration. The fermentation medium contained 1 g/L yeast extract, 1 g/L peptone at 4.5 pH. The production medium was supplemented with 1.0 mL of the recombinant cellulase obtained from E.coli in order to hydrolyze the substrate. Flasks were inoculated with 1% (v/v) S. cerevisiae culture obtained by growing the organism on a rotary shaker at 120 rpm for 48 h at 30°C in GYE medium. The samples were taken every 6 h and analyzed for enzyme activity, protein concentration, cell growth, glucose, and ethanol production.
2.7. Effect of Operational Parameters on SSF
The effect of temperature on ethanol production by simultaneous saccharification and fermentation process using S. cerevisiae was carried out by varying the temperature between 30°C–40°C. The effect of enzyme with 1 mL, 2 mL, and 5 mL having concentration (0.55 mg/mL) and specific activity of 0.52 U/mg on ethanol production was also investigated.
2.8. Analytical Methods
The enzyme assay was carried out by incubating the enzyme with substrate for 10 min at 50°C. The reaction mixture (100 μL) contained 10 μL of supernatant containing enzyme and 1% final carboxymethyl cellulose (CMC) in 0.02M sodium acetate buffer, pH 4.3. The 100 μL reaction mixture was then analyzed for the release of reducing sugar using the Nelson and Somogyi, method [15, 16]. Glucose was used as standard. Protein content was determined using 10 μL of enzyme and 90 μL of distilled water. To the 100 μL of mixture 1 mL Bradford reagent was added. The reaction mixture was incubated at room temperature for 20 min and then analyzed spectrophotometrically at 595 nm . BSA was used as standard. Ethanol content was estimated by using 1 mL cell-free supernatant to which 9 mL distilled water and 1 mL dichromate was added and heated for 10 min in boiling water bath. During heating, ethanol was converted to acid on reaction with dichromate and resulted in colour change from orange to green which can be analysed spectrophotometrically at 600 nm . Ethanol was used as standard.
3. Results and Discussion
3.1. Production and Enhancement of Recombinant Cellulase from E. Coli
The maximum OD, enzyme activity, and specific activity obtained in batch mode were 1.62, 0.136 U/mL, and 1.91 U/mg, respectively, as shown in Figure 1(a). In the fed-batch mode, maximum OD, enzyme activity, and specific activity obtained was 3.78, 0.301 U/mL, and 3.52 U/mg, respectively, as shown in Figure 1(b). Thus, the fed-batch cultivation of E. coli containing recombinant enzyme displayed two-fold increase in biomass productivity, the enzyme activity, and specific activity in comparison to a batch cultivation process. During fed-batch mode, already induced cells were used as inoculum for the consecutive batches due to which more protein expression was observed and due to further induction by the addition of IPTG more recombinant enzyme was produced.
3.2. Ethanol Production by SSF from Substrates Using Different Pretreatment
The solid residues of various substrates were subjected to SSF process by S. cerevisiae at a temperature of 30°C and 1.0% substrate concentration after pretreatment. The pretreated substrates were hydrolyzed enzymatically by recombinant cellulase isolated from recombinant E. coli cells. All pretreatments were efficient for delignification of the lignocellulosic biomass. The effect of different pretreatments on ethanol production is shown in Table 1. In all cases of substrates, low-reducing sugar contents were obtained with good yeast fermentation performance. Depending on the amount of ethanol produced, acid pretreatment was found to be the best of all pretreatment methods carried out. Recent studies have shown that when acids are combined with alkali, they play more effective role in LCW pretreatment than acids or alkalis alone . Using steam explosion as pretreatment, maximum ethanol was produced in case of eucalyptus (0.53 g/L) with a yield coefficient of 0.053 followed by jamun (0.46 g/L ethanol) and yield coefficient of 0.046 (Table 1). Using alkali pretreatment method maximum ethanol was obtained in case of bamboo (0.83 g/L) with a yield coefficient of 0.083 followed by wild grass (0.77 g/L ethanol) and yield coefficient of 0.077 (Table 1). Using acid method as a pretreatment strategy, maximum ethanol was obtained in case of jamun (1.22 g/L) with a yield coefficient of 0.122 followed by wild Grass (0.78 g/L) with a yield coefficient of 0.078 as shown in Table 1. Hence, acid pretreatment gave best results of the three different pretreatments carried out, as in case of acid pretreatment both acid and alkali are used, which resulted in higher delignification of the substrates. By acid pre-treatment, the structure of substrate becomes less complex, and it becomes more accessible to the enzyme, and hence, more reducing sugars are released. These sugars are then converted to ethanol by yeast, the fermenting organism. The ethanol concentration of 21 g/L was obtained using commercial cellulolytic enzyme and 10% (w/v) substrate (sunflower stalks), that is, 2.1 g/L ethanol concentration with 1% substrate . Kinnow waste and banana peels were used as substrates in the ratio of 6: 4, and total 25 g biomass was obtained 26.84 g/L ethanol, that is, 1.074 g/L ethanol by using 1 g of biomass . Using baggase as substrate the ethanol yield of 0.13–0.18  and 0.116  were obtained which are comparable to our findings. The ethanol concentration of 22 g/L was obtained using coculture of Clostridium thermosaccharolyticum HG8 and Thermoanaerobacter ethanolicus ATCC 31937 with 100 g/L banana waste as substrate, that is, 2.2 g/L of ethanol from 1% of substrate . All these results are comparable with our findings though we are using recombinant enzyme which is cost effective as compared to above mentioned methods.
3.3. Effect of Temperature and Enzyme Concentration on Ethanol Production by SSF
Since acid pretreatment gave the best results out of three pretreatments, so for temperature optimization using acid pretreatment was done for SSF. Four substrates, jamun, bamboo, eucalyptus, and wild grass, were selected for optimization, since these gave better results over as compared to other substrates. The effect of temperature on ethanol production by simultaneous saccharification and fermentation using S. cerevisiae was studied at temperatures 30°C, 35°C and 40°C. Maximum ethanol was obtained with Syzygium cumini (Jamun) as a substrate at 30°C (Figure 2). Using jamun as a substrate ethanol obtained at 30°C, 35°C, and 40°C was 1.2 g/L, 0.46 g/L and 0.41 g/L, respectively. However, at temperatures higher than 30°C showed a fall in ethanol production which is consistent with the findings of El-Refai et al.  who reported maximum ethanol productivity from beet molasses by S. cerevisiae Y-7. The temperature, 30°C has been also reported as optimum for maximum ethanol production using starch employing coculture of amylolytic yeast and S. cerevisiae . These observations are consistent with findings of other authors [25, 26]. The future experiments were conducted at incubation temperature of 30°C. The effect of crude cellulase 1 mL, 2 mL, and 5 mL (0.53 U/mg, 0.55 mg protein/mL) on ethanol production was investigated. Using jamun, ethanol obtained at 1 mL, 2 mL, and 5 mL enzyme concentration was 1.26 g/L, 1.27 g/L, and 1.43 g/L, respectively, showing no significant effect of enzyme concentration on ethanol production (Figure 3). The enzymatic hydrolysis of the solid fraction has large control over total rate of ethanol production in SSF [27, 28]. Studies in which the enzyme loading has been varied showed strong positive correlation between enzyme loading and the overall ethanol yield [29, 30].
3.4. Effect of Cell Growth on Ethanol Production
S. cerevisiae stays in the lag phase during the initial 12 to 16 h from inoculation due to the unavailability of utilizable sugars in the medium. Hydrolysis of the complex cellulose takes place during the initial 18 h in which the organism lies in the lag phase of growth. Cellobiose is the direct product of the cellulose activity which is an inhibitor of the enzyme. Kovacs et al.  report the need to supplement commercial cellulases used in SSF process with β-glucosidase and also observed the accumulation of cellobiose nearly to 10 g L−1 during the first 10 h of fermentation, when using the bakery S. cerevisiae strain for bioethanol production in SSF process with sugarcane bagasse, and had to add additional β-glucosidase in their experiments to reduce the cellobiose concentration. For next 24 h, S.cerevisiae enters the log phase utilizing the consumable sugars derived from cellulose, which, in turn, increased the percentage of ethanol produced during fermentation. Ethanol production reaches the maximum during the stationary phase of the organism. Maximum amount of reducing sugar was obtained in the lag phase and then in the stationary phase which was utilized for the growth and maintenance of the microorganism, respectively. SSF profile of jamun using acid pretreatment at 30°C is shown in Figure 3.
The use of recombinant cellulase for bioethanol production is a strategy to reduce the enzyme cost. The in vitro cellulase production and activity can be enhanced using the fed-batch mode. This study could establish that the agricultural wastes which have considerable disposal problem can be used for ethanol production through the process of simultaneous saccharification and fermentation. Thus, the present study opens new possibilities of exploiting leafy litter commercially for industrial applications. There is certainly the scope of enhancing the ethanol yield by process optimization. The process with optimized fermentation conditions can then be used for scaling up to the pilot scale.
The research work was supported by a joint project grant from Department of Biotechnology, Ministry of Science and Technology, New Delhi, India, to A. Goyal and D. Goyal.
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