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9 Submitted Date: September 12, 2009 Accepted Date: October 12, 2009
Correcponding Author: Dr. J. S. Ghosh, Dept of Microbiology, Shivaji University, Kolhapur 416004.Ph: +91 9850515620 35
Adv. J. Food Sci. Technol., 1(1): 35-38: 2009 Estimation of Titrable Acidity: The titrable acidity of all samples are detected as per (IS: 11766, 1986), which is the average results of 12 sam ples of each products (Fig. 3). Microbiological analysis: The samples were homogenized in a blender using sterile physiological saline (0 .85% NaCl solution). Coliform count: The supernatant of the above mentioned suspension was diluted 1:10 and was directly plated on Violet Red Bile Agar (IS: 5404, 1995). The inoculated plates of this medium were incubated 37C for 48 h (Fig. 4). In case of suspected colonies, the sam ples were then enriched in B rilliant G reen L actose Bile Broth (BGLB) having dehydrated ox bile-2%, lactose-1%, peptone-1% and 1 .3 mL of 1.0 % solution of brilliant green in water, final pH 7.2. The tubes were incubated at 37C for 48 h . This growth in these tubes were then inoculated on Hicrome E. coli agar (Hi Media L td., Bom bay). The plates were incubated at 30C for 4 h and then at 44C for 18 h (Tab le 1). Micrococcus aureus: Since milk is very good nutrient for Micrococcus aureus, the supernatant of the homogenized samples were subjected to detection of this microorganism, which is a potent exotoxin producer (Draft ISO/DIS 6888, 1983). The isolates were checked for coagulase positive nature using defibrinated plasma (Table 2). Salmonella: Detection of Salm onella were carried out as per the prescribed metho d of (IS: 5887, 1999). Shigella : The presence or absence of Shigella spp. was carried out as per (IS: 5887, 199 9). Listeria monocytogenes : The de tection of Listeria monocy togenes was don e as per (ISO 10560, 19 99). RESULTS AND DISCUSSION It can be seen from the Fig. 1 that only in case for shrikhand and fruit shrikhan d, there is a large unjustifiable deviation from the standard, which often does more ha rm than good. It is only in case of shrikhand and amrakhand, that titrabele acidity is below standard which might pose not only a threat of spoilage by microorganisms, but allow food poisoning organisms like Micrococcus aureus to grow and make the product hazardous. (Fig. 3) It may be noted from the F ig. 2 that Mo isture contents of the products men tioned are w ell within limits. How ever, since th ere are no standards for D ahi and Lassi, these parame ters were not checked as there is no means of com parison.
Fig. 1: Fat content of the products examined. The standard values are as per PFA-1954 (2009)
Fig. 2: Moisture of the different products. The standard values shown in figure are as per PFA-1954 (2009)
Fig. 3: Titrable acidity of the different products. The standards as shown in the figure are as per PFA-1954 (2009)
Fig. 4: Coliform count of different products. The standards shown above are as per PFA-1954 (2009)
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Shigella/gm ND ND ND ND ND ND ND ND ND ND ND ND
Shigella /gm ND ND ND ND ND ND ND ND ND ND ND ND
Table 3: Microbiological analysis of Shrikhand with mango pulp samples Sr. No. En t E. co li /gm Salmonella /gm Shigella /gm 1. 2. 3. 4. 5. 6. 7. 8. 9. 10. 11. 12. ND : Not Detected ND ND ND ND ND Present ND ND ND ND ND ND ND ND ND ND ND ND ND ND ND ND ND ND ND ND ND ND ND ND ND ND ND ND ND ND
It is vivid from the results above that 3 out of 4 products shows high coliform count which is detrimental to the safe ty of the product, from public health point of view (Fig.4). It can be seen from Table 1, that enteric E. coli was present in 5 out of 12 samples and Micrococcus aureus is present in 2 out of 12 samp les. This means that chances of contracting an enteric disease through consumption of such curds is nearly 50% Shrikhand is a sweetened product made out of hung curd, but the sugar is used as a flavouring agent rather than reduc ing w ater activity. However, there are certain spices like crushed cardamom seeds, the oleoresins of which would inhibit the growth of many microorganisms
and that is why it is observed from Table 2, that 4 out of 12 samples which were really prepared in unhygienic conditions show s the presenc e of E. coli and 2 shows the presence of Micrococcus aureus. Therefore, this product has more chan ces of giving food poisoning cases as Micrococcus aureus is a potent exo toxin p roducer. This is a product like shrikhand. The only difference is that it contains actual Alphonso mango pulp. Ag ain the point that is to be noted from Table 3, is that, there is presence of Micrococcus aureus which is a potent exotoxin producer, capable of causing food poisoning. In fruit shrikhand, pineapple, grape, apple and pom egran ate was found to have been added shrikhand. Table 4 show that 2 samples were found to be safe as only one of it show ed the presence of E. coli.
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Table 5: Microbiological analysis of Lassi samples Sr. No. En t E.co li /ml Salmonella /ml 1. 2. 3. 4. 5. 6. 7. 8. 9. 10. 11. 12. ND : Not Detected Present Present Present Present Present ND ND ND ND Present ND Present ND ND ND ND ND ND ND ND ND ND ND ND
Shigella /ml ND ND ND ND ND ND ND ND ND ND ND ND
This product is prepared from curd, which was mixed with water to get certain pulp density. There is no standard for the pulp density and due to this every manufacturer would add any amount of water they like as long as they the customers for their product. There is also presence of sugar in this product. Table 5 show that out of 12 samples the re are about 7 sam ples co ntaining enteric E. coli and 4 ou t of 12 con tained Micrococcus aureus. Production of this is mo stly in the unorganized sector and hence there is no brand that needs to be pu t nor there is any need for a definite retail outlay to sell this prod uct. All this factors make the manufacturer free to add any water they like and these contam inants are from the water. CONCLUSION Mo st of the Indigenous fermented milk products are prepared by traditional methods in the unorganized industrial sector. Such methods often bring about contamination of various microorganisms including pathogens. To overcome these problems these traditional methods are automated in different organized sectors which shou ld hav e helped to improve the microbiological quality of the products. However, due to high cost of capital investment, a sizeable portion of these products are still produced in the unorganized sectors, many of which do not even have the necessary licenses to do so and hence are not bound by any law of product safety. These are, more than often, not branded and the volume of sales are significantly high but localized regionally. This has resulted in poo r microbiolog ical quality with respe ct to presence of pathogens and spoilage organisms. Therefore, If the taste and flavors of these tradional flavors is to be maintained traditionally, the producers of these high risk
products should be educated in the minimum requirements of good hygienic and sanitary conditions, good manufacture practices and good storage conditions which will reduce the risk of poor microbiological quality and increase the safety of the products. REFERENCES Aneja, R.P., B.N. Mathur, R.C. Chandan and A.K. Banerjee, 2002. Technology of Indian Milk Products; A D airy Ind ia Pub lication, D elhi. Draft ISO/DIS 6880, 1983. International Organization for S t a n d a r d i z at i o n ( I S O ) , e n u m e r a t io n o f Staphylococcus aureus. IS: 7035, 1973. Specification for ferm ented milk products. N ew Delhi. IS: 1224, 1977. Part-II, Determination of Fat by Gerber Method: Milk Prod ucts Indian Standards Institution,. Manak Bhavan New D elhi. IS: 11766, 1986/ISO: 6092, 1980. M ethod for determination of titratable acidity in milk powder and similar products (routine method ). IS: 11623, 1986. Re-1997, Method for determination of moisture content in milk powder and similar products. IS: 5404, 1995. Methods for drawing and handling of food samples for microbiological analysis. IS: 5887, 199 9. Part 3. Method s for detection of bacteria respo nsible for food poisoning. ISO 10560, 1999. Milk and milk products-Detection of Listeria monocytoge nes. Bratislava. pp: 24. PFA (Prevention of Food Adulteration Acts (India)-1954, 2009. Food Safety Laws, International Law Book Publishers, N ew Delhi.
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