International Journal of Food Science

International Journal of Food Science / 2014 / Article

Research Article | Open Access

Volume 2014 |Article ID 408085 |

Kamal Rai Aneja, Romika Dhiman, Neeraj Kumar Aggarwal, Vikas Kumar, Manpreeet Kaur, "Microbes Associated with Freshly Prepared Juices of Citrus and Carrots", International Journal of Food Science, vol. 2014, Article ID 408085, 7 pages, 2014.

Microbes Associated with Freshly Prepared Juices of Citrus and Carrots

Academic Editor: Rosana G. Moreira
Received24 Jun 2014
Revised22 Sep 2014
Accepted06 Oct 2014
Published19 Oct 2014


Fruit juices are popular drinks as they contain antioxidants, vitamins, and minerals that are essential for human being and play important role in the prevention of heart diseases, cancer, and diabetes. They contain essential nutrients which support the growth of acid tolerant bacteria, yeasts, and moulds. In the present study, we have conducted a microbiological examination of freshly prepared juices (sweet lime, orange, and carrot) by serial dilution agar plate technique. A total of 30 juice samples were examined for their microbiological quality. Twenty-five microbial species including 9 bacterial isolates, 5 yeast isolates, and 11 mould isolates were isolated from juices. Yeasts and moulds were the main cause of spoilage of juices. Aspergillus flavus and Rhodotorula mucilaginosa were observed in the maximum number of juice samples. Among bacteria Bacillus cereus and Serratia were dominant. Escherichia coli and Staphylococcus aureus were detected in few samples. Candida sp., Curvularia, Colletotrichum, and Acetobacter were observed only in citrus juice samples. Alternaria, Aspergillus terreus, A. niger, Cladosporium, and Fusarium were also observed in tested juice samples. Some of the microorganisms detected in these juice samples can cause disease in human beings, so there is need for some guidelines that can improve the quality of fruit juices.

1. Introduction

Unpasteurized fruit juice is defined as the product produced by pressing or squeezing of the fruits [1]. Consumption of fresh juices increased dramatically due to their freshness, high vitamin content, and low caloric consumption [2]. Extracted juices from fruits contain most substances which are found in the original ripe and sound fruit from which the juice is made. The high potassium and low sodium characteristic of most juices help in maintaining a healthy blood pressure. Vitamin C is naturally present in juices which are essential for the body to form collagen, cartilage, muscle, and blood vessels. It also helps in the absorption of iron [3].

Fruit juices contain a microflora which is normally present on the surface of fruits during harvest and postharvest processing which include transport, storage, and processing [4]. Many microorganisms such as acid tolerant bacteria and fungi (moulds, yeasts) use them as a substrate for their growth. Yeasts form the main flora of fruits before processing because of acidic pH. The major genera include Candida, Dekkera, Hanseniaspora, Pichia, Saccharomyces, and Zygosaccharomyces. Penicillium, Byssochlamys, Aspergillus, Paecilomyces, Mucor, Cladosporium, Fusarium, Botrytis, Talaromyces, and Neosartorya are filamentous fungi most frequently isolated from fresh fruits and juices. Among bacteria, lactic acid bacteria and acetic acid bacteria have been isolated from fruit juices [5].

The critical factors affecting the spoilage of juices include juice pH, oxidation reduction potential, water activity, availability of nutrients, presence of antimicrobial compounds, and competing microflora. Among these factors, pH and water activity are the most influential factors affecting the spoilage of juices. The spoilage caused by microorganisms in juices includes cloud loss, development of off-flavours, CO2 production, and changes in colour, texture, and appearance resulting in degradation of product [6, 7]. The most commonly reported bacterial genera include Acetobacter, Alicyclobacillus, Bacillus, Gluconobacter, Lactobacillus, Leuconostoc, Zymomonas, and Zymobacter. Among yeasts Pichia, Candida, Saccharomyces, and Rhodotorula are commonly encountered genera responsible for spoilage of juices [8]. Certain common moulds such as Penicillium sp., Aspergillus sp., Eurotium, Alternaria, Cladosporium, Paecilomyces, and Botrytis have also been reported in spoilage of fruit juices [5, 6].

Fruit juices have pH in the acidic range (<4.5) serving as important barrier for microbial growth. However, food borne pathogens such as E. coli and Salmonella survive in acidic environment of fruit juices due to acid stress response. Therefore, in the last two decades a number of food borne outbreaks associated with unpasteurized fruit juices have been documented in many countries [1, 9]. The source of entry of microorganisms into fresh fruit juices from environment exposure and soil. In developing country like India, a large population of all income and age groups consume freshly squeezed fruit and vegetable juice [10], but the presence of pathogenic microorganisms in street vended fruit juices has also been reported in various parts of India such as Vishakhapatnam [11], Mumbai [12], Amravati [13], and Nagpur [10]. In view of the demand for fresh fruit juices throughout the year and threat of emerging food borne outbreaks associated with consumption of fruit juices, the aim of present study was to investigate the microbiological examination of freshly prepared juices commonly consumed in Kurukshetra.

2. Materials and Methods

2.1. Fruit Juice Preparation

Three juices commonly consumed in Kurukshetra such as orange (Citrus reticulata Blanco), sweet orange (Citrus sinensis), and carrot (Daucus carota) were selected for microbiological study. Sweet orange, carrot, and orange were purchased from the local markets of Kurukshetra from October 2011 to February 2012. Each sample was washed, peeled, and cut into pieces and juice was extracted through sterile hand blender and poured into sterile beaker.

2.2. Measurement of pH

The pH of juice samples was measured using a pH meter.

2.3. Microbiological Analysis

The microbiological study of fruit juices was done by serial dilution agar plate technique. Ten mL of juice sample was diluted with 90 mL of 0.1% sterile peptone water (1 g peptone, 1L distilled water) and plated on nutrient agar (pH 5.5) for enumeration of bacteria and PDA supplemented with antibiotic (pH 5.5) for enumeration of fungi in duplicates [4]. Uninoculated plates of PDA and NA were used as control. Mould and yeast isolates were purified on potato dextrose agar, bacteria on nutrient agar, and further subcultured for microscopic examination and identification.

2.4. Identification of Bacteria

For bacterial identification, 24-hour-old culture of bacteria was observed under microscope by gram stain method and further various biochemical tests were performed for the identification of bacteria such as catalase test, oxidase test, starch hydrolysis test, sugar fermentation test, IMViC test, and methods described in “Bergey’s Manual of Systematic Bacteriology” [14]. Further identification of bacteria was performed on the basis of methods described in “Compendium of methods for the microbiological examination of foods” [15, 16].

2.5. Identification of Yeasts

The methods adopted for identification of yeasts include morphological characteristics, fermentation of sugars, germ tube test and cycloheximide resistance test, and methods described in “Fungi and Food Spoilage” [17, 18].

2.6. Identification of Moulds

Moulds were identified on the basis of morphological and cultural characteristics such as colour of the colony, surface, appearance, presence, and absence of cross walls, and asexual and sexual reproductive structures. Further identification of moulds was carried out according to the methods described in “Fungi and Food Spoilage.” Moulds were cultured on Czapek yeast extract agar (pH 6.7), Malt extract agar (pH 5.6), and Glycerol nitrate agar (pH 7.0) at 25°C.

3. Results and Discussion

In the present study, 30 samples of freshly prepared juices (10 samples each of orange, sweet orange, and carrot) were examined for microbiological analysis. The pH range of juices is shown in Table 1. Factors which determine the colonization of juices by microorganisms include pH, redox potential, water activity, nutrients, structures, antimicrobial agents, temperature, relative humidity, and atmosphere [1]. In the present study the frequencies of occurrence of moulds and yeasts were more as compared to bacterial genera which is attributed to low pH values and high sugar content [19].

Juices pH rangeMean

Orange 4.19–4.504.34
Sweet lime 4.70–5.475.08
Carrot 5.76–6.035.89

A total of 34 bacterial, 12 yeast, and 25 mould isolates were isolated from juices classified by grouping them into 9 bacterial species, 5 yeast species, and 11 mould species on the basis of phenotypic characteristics. Morphological and biochemical properties of bacteria were explained in Tables 2 and 3. Details of morphology and physiology of yeasts were described in Tables 4 and 5. Colonial and microscopic characteristics of various moulds were summarized in Tables 6 and 7.

Bacterial isolates Colour on nutrient agar Configuration Margin Elevation Gram reaction Shape of isolate Endospore staining

Bacillus subtilis WhiteCircular lobate Irregular Flat Positive Rods in chainsCentral spore
B. cereus Off-white Circular Entire Convex PositiveRods in chainsCentral spore
Escherichia coli Mucoid Circular Entire Slightly raised Negative Rods
Serratia Mucoid Circular Entire Umbonate NegativeRods
Leuconostoc Light yellowCircular Entire Convex PositiveCocci
Micrococcus Bright Yellow Circular Entire Convex PositiveCocci shape in tetrad
Staphylococcus aureus Golden yellow colourCircular pin head colonies Entire ConvexPositiveCocci in grapes like bunches
Lactobacillus White Circular Entire Raised PositiveRods
Acetobacter Pale Circular Entire Flat NegativeRods

—: absent.

Bacterial isolates Catalase Oxidase Starch hydrolysisIMViC testSugar fermentation
Indole Methyl red Voges-ProskauerCitrate Glucose Lactose Mannitol Sucrose

Bacillus subtilis ++++AAA
B. cereus ++++AA
Escherichia coli +++A + GA + G
Serratia ++A+
Leuconostoc ++AA
Micrococcus ++++AA
Staphylococcus aureus +++AAAA
Lactobacillus A + GA
Acetobacter ++A

+: positive; −: negative; A: acid; A + G: acid + gas.

Yeast isolates Colour on PDAConfiguration Margin Microscopic features

Pichia Off-white Hemispherical Irregular Ellipsoidal to cylindrical; reproducing by irregular budding
Saccharomyces Off-whiteCircular Irregular Spherical to subspheroidal; reproducing by irregular budding
Candida krusei White Circular Irregular Ellipsoidal to long cylindrical; reproducing by irregular budding
Rhodotorula Pink Circular or spreading Regular Ellipsoidal shape; reproducing by irregular budding
Candida parapsilosis White to cream Circular Regular Globose to ovoid budding

Yeast isolate Germ tube testCycloheximide resistance Sugar fermentation*
Glucose Sucrose Lactose Maltose

Pichia +++
Saccharomyces ++
Candida krusei +
Candida parapsilosis +

+: positive; −: negative; *fermentation means production of gas independent of pH changes.

Mould isolate Colony colour on PDA on front side Colony colour on PDA on reverse sideMicroscopic features

Aspergillus flavus Yellow green Colourless Conidiophores arise separately from foot cell, phialides uniseriate and sometimes biseriate; conidia globose to subglobose

A. terreus BrownColorlessConidiophore borne from surface hyphae, stripes long, and smooth walled; vesicles with densely packed, short, narrow metulae and phialides; conidia unicellular, spherical, and very small

A. niger Black Creamy Hyphae septate and hyaline, smooth walled conidiophores arising from foot cell; vesicles globose, whole vesicle fertile bearing two series of sterigmata; catenate conidia arranged in basipetal manner, unicellular, and globose

Penicillium islandicum Ivy green CreamyShort conidiophores bearing a compact verticil of metulae, phialides closely packed in clusters bearing catenate conidia arranged in basipetal manner, conidia elliptical, smooth, and hyaline

P. digitatum Green Colourless Conidiophores borne from surface and aerial hyphae with thin smooth walls; bearing terminal penicilli; terverticillate but frequently biverticillate or irregular

Alternaria Black Colourless Small to large sized conidia with beak; arising in chains in acropetal manner with both transverse and longitudinal septa

Cladosporium BlackColourlessConidiophore tall, dark upright, and branched variously near the apex, conidia 1-2-celled ovoid to cylindrical shape

Colletotrichum Cottony white to pale gray mycelium Colourless Acervuli disc shaped, typically with dark spines or setae at the edge of conidiophores; conidiophores simple, elongate conidia single celled, hyaline or brightly coloured, cylindrical or pointed, straight or curved

Curvularia Green to black BlackSimple conidiophores bearing spores apically; Conidia dark, end cells, 3–5-celled; more or less fusiform, typically bent

Fusarium Wooly white Colourless Conidiophores slender and simple, short or branched irregularly or bearing a whorl of phialides; conidia hyaline, variable, principally of two kinds, macroconidia several celled slightly curved or bent at the point ends, microconidia 1-celled, ovoid or oblong, borne singly or in chains

Geotrichum White ColourlessConidia borne solely by the breakup of hyphae to form arthroconidia

Mould isolateColony colour on CYAColony colour on MEAColony colour on G25N
Front side Reverse side Front side Reverse sideFront side Reverse side

Aspergillus flavus Yellow green Colourless Yellow green Colourless Yellow green Colourless

A. terreus Brown Dull brown Brown Dull brown Brown Dull brown

A. niger Black Pale to bright yellow Black Pale to bright yellow Black Pale to bright yellow

Penicillium islandicum Greyish greenOrange to rust brown central areaGreyish greenOrange to rust brown central areaGreyish greenOrange to rust brown central area

P. digitatum Greyish green to olive Pale or brown Dull yellow green Pale or brownGreen olive Pale

Alternaria Grey to blackBlack Grey to blackBlack Grey to blackBlack

Cladosporium Olive to dark olive Grey Olive Grey Olive Black

Colletotrichum Grey Pale grey Grey Pale grey Black Grey

Curvularia Off-white to grey Grey Off-white to grey Grey Grey to blackGrey

Fusarium White to grayish rose Pale White Pale White Pale

Geotrichum White Pale White Pale No growth

Yeasts and moulds are capable of growth at pH values of 1.5 and at water activity values below 0.89. The minimum pH values allowing the growth of lactic acid bacteria (pH 2.9–3.5), acetic acid bacteria (pH 3.0–4.5), and enteric bacteria (pH 3.6–4.5) are higher than those for growth of yeasts and moulds [6].

The frequency of occurrence of bacteria, yeasts, and moulds are summarized in Tables 8, 9, and 10, respectively. The occurrence of bacterial genera ranged from 10% to 56% (Table 8). Bacillus cereus and Serratia sp. were detected in a greater number of samples. Bacillus cereus was also observed in 64.91% of samples of unpasteurized street vended fruit juices [20]. Leuconostoc and Lactobacillus were also reported as important group of spoilage microorganisms in acidic products [21]. The presence of lactic acid bacteria more frequently occurs in unpasteurized juices [22]. These microorganisms produce acetic and formic acids along with ethanol and carbon dioxide which can alter the flavor of juice [23]. Leuconostoc, Lactobacillus, and Acetobacter were detected in tested juice samples (Table 8).

Bacterial isolatesOrange juice
Sweet orange juice
Carrot juice
Total number of samplesPercentage frequency

Bacillus subtilis 5341240%
B. cereus 8451756.7%
Escherichia coli 231620.0%
Serratia 5541446.7%
Leuconostoc 45930.0%
Micrococcus 3310.0%
Staphylococcus aureus 212516.7%
Lactobacillus 232723.3%
Acetobacter 35826.7%

—: absent.

Yeast isolates Orange juice
Sweet orange juice
Carrot juice
Total number of samples Percentage frequency

Pichia 8741963.3%
Saccharomyces 6841756.67%
Candida krusei 381136.7%
Rhodotorula 9692480%
Candida parapsilosis 8826.7%

—: absent.

Mould isolates Orange juice
Sweet lime juice
Carrot juice
Total number of samples Percentage frequency = occurrence in observed samples/total no of samples

Aspergillus flavus 9972583.3%
A. terreus 5741653.3%
A. niger 321620%
Penicillium islandicum 9772376.7%
P. digitatum751240%
Alternaria 6531446.7%
Cladosporium 342930%
Colletotrichum 53826.7%
Curvularia 32516.7%
Fusarium 4631343.3%
Geotrichum 43723.3%

—: absent.

The presence of E. coli, Salmonella, and S. aureus in fruit juices is primarily concern because these pathogens were implicated in a number of outbreaks associated with fruit juices [1]. In our study, the presence of E. coli and S. aureus was detected in a smaller number of samples. The survival of pathogens in acidic environment of juices is attributed to their ability to regulate their internal pH and maintained at neutral pH by combination of passive and active homeostasis mechanisms [24]. The acid survival mechanisms of enteric bacteria are due to induction of enzymes that are involved in raising the internal pH and activation of enzymes devoted to the protection and repair of proteins and DNA [25].

Yeasts genera responsible for spoilage of fruit juices include Candida, Pichia, Rhodotorula, Torulopsis, Saccharomyces, Zygosaccharomyces, Hansenula, and Trichosporon [26]. In our study, the dominant yeasts isolated from juices were Rhodotorula, Pichia, and Saccharomyces (Table 9). Rhodotorula was found in maximum number of juice samples tested followed by Pichia and Saccharomyces. Candida parapsilosis and C. krusei were only detected in orange and sweet orange juices, not detected in carrot juice. Ghenghesh et al. [9] also reported the presence of Candida sp. in 58% of orange juice samples. Rhodotorula, Pichia, Candida, and Saccharomyces have also been reported as spoilage causing organisms in pasteurized fruit juices [4, 27]. Yeast spoilage in fruit juices is characterized by formation of CO2 and alcohol. Yeasts may also produce turbidity, flocculation, pellicles, and clumping. Yeasts also produced pectin esterases which degrade pectin causing spoilage; organic acids and acetaldehyde, which contribute to a “fermented flavor,” may also be formed [5, 6].

The dominant moulds recorded in fruit juices belong to Penicillium sp., Cladosporium sp., Aspergillus niger, A. fumigatus, Botrytis sp., and Aureobasidium pullulans. They produce mycelial mats and musty, stale off-flavours in juices [6]. Rhizopus and Mucor are also associated with spoilage of fresh fruits and vegetables [28]. In the present study, the most frequently encountered moulds were Aspergillus flavus, A. terreus, and Penicillium islandicum (Table 5). P. digitatum, Colletotrichum, and Curvularia were isolated from orange and sweet orange juices. Geotrichum was detected in orange and carrot juice. Spoilage by moulds in fruit juices is characterized by loss of juice cloud [6]. Among these, some moulds produce mycotoxins which are of great threat to human health. Major mycotoxins associated with fruit juices are byssochlamic acid (Byssochlamys fulva, B. nivea), patulin (B. fulva, B. nivea, and P. expansum), ochratoxin (Aspergillus carbonarius), and citrinin (Penicillium expansum, P. citrinum) [29, 30].

4. Conclusion

Juices squeezed from fresh fruits and vegetables contain microorganisms which are potentially hazardous to public health. Juices were spoiled with high level of moulds and yeasts which is attributable to low pH of juices. The presence of pathogenic microorganisms in juices is clearly indication of food borne outbreaks. The selling and consumption of juices are never stopped on nutritional grounds as well as livelihood of street vendors. It is alarming situation for suitable agency to take some necessary action, make guidelines to prevent potential food poisoning from juices that contain pathogenic bacteria, and find natural antimicrobials from plants that control spoilage and pathogenic microorganisms in juices.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.


The authors are thankful to Kurukshetra University, Kurukshetra, for the financial assistance.


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Copyright © 2014 Kamal Rai Aneja 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.

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