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picture1_Total Plate Count Method Pdf 85524 | Mesophilic Aerobic Bacteria Standard Plate Count Or Total Plate Count


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File: Total Plate Count Method Pdf 85524 | Mesophilic Aerobic Bacteria Standard Plate Count Or Total Plate Count
1 microbiological methods i a mesophilic aerobic bacteria standard plate count or total plate count principle viable bacteria are quantitated by the fractional gram pour plate technique scope the method ...

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                                                                                       1
            Microbiological Methods                                                                                          I-A-  
                                                   
                                                   
                                  MESOPHILIC AEROBIC BACTERIA 
                        (STANDARD PLATE COUNT OR TOTAL PLATE COUNT) 
             
             
            PRINCIPLE 
             
                  Viable bacteria are quantitated by the fractional gram pour plate technique. 
             
            SCOPE 
             
                  The method is applicable to starches, syrups and sugars and most coproducts of 
                  the corn wet milling industry. 
                   
            MEDIA AND REAGENTS 
             
                  1.    Plate Count Agar (PCA).  Prepare according to the manufacturer's 
                        directions. 
             
                  2.    Butterfield's Phosphate Diluent 
             
                        Stock Solution:  Dissolve 34 g of potassium dihydrogen phosphate 
                        (KH2PO4) in 500 mL of purified water, adjust to pH 7.2 with about 175 mL 
                        of 1N NaOH solution and dilute to 1 L volume.  Store under refrigeration. 
             
                        Diluent:  Dilute 1.25 mL of stock solution to 1 L volume with purified 
                        water.  Prepare dilution blanks using this solution. 
                   
                  3.    Water Dilution Blanks.  Fill water dilution bottles to 80, 90, or 99 mL with 
                        Butterfield's Phosphate Diluent.  Cap bottles and sterilize at 121°C, at 15 
                        pounds pressure for 15 mins. in a steam autoclave (Note 1). 
             
                  4.    Sodium Hydroxide Solution, 1N. 
             
                            Microbiological Methods of the Member Companies of the 
                                        Corn Refiners Association 
                                            Accepted 03-20-91 
                                             Revised 02-01-07 
                                                                                      2
            Microbiological Methods                                                                                          I-A-  
                                                  
                                                  
                                  MESOPHILIC AEROBIC BACTERIA 
                  (STANDARD PLATE COUNT OR TOTAL PLATE COUNT) ⎯ continued 
                                                  
                                                  
            PROCEDURE 
             
                  Two common fractional gram sample dilution techniques may be used for any 
                  given sample.  The number of dilutions depends on the individual sample and may 
                  be determined by past experience. 
                   
                  A.    Factor Five Dilution Series (FFS):  Aseptically weigh 20 g of the sample 
                        into a sterile 80 mL water blank and homogenize.  This is the primary 1:5 
                        dilution blank (PDB).  Twenty mL of the PDB can be aseptically 
                        transferred to another sterile 80 mL water blank, and the sample is diluted 
                        by a factor of 25. 
                   
                  B.    Factor Ten Dilution Series (FTS): The same as FFS only 10 g of sample 
                        and 90 mL sterile water blanks are used.  The sample is diluted by a factor 
                        of 10, 100, 1000, etc. 
             
                        Aseptically dilute the sample by either FFS or FTS (Note 3).  Pipet 
                        aseptically 1 mL of each dilution to appropriately marked duplicate Petri 
                        dishes.  Pour 15-20 mL of the PCA agar which has been cooled to 45°C 
                        into each dish.  Swirl plates and allow to solidify. 
             
                        Invert the plates and incubate at 35-37 °C for 48 ± 3 hrs.  Count the number 
                        of colonies on those plates showing 25-250 colonies (Note 4).  Average the 
                        count of the duplicate plates, multiply by the dilution factor and record as 
                        the number of bacteria per gram or as Standard Plate Count per gram.  If 
                        the lowest dilution shows less than 25 colonies, then these colonies must be 
                        counted and reported (Note 5). 
             
            CALCULATION 
             
                  Number of bacteria per gram = Average number of bacteria x Dilution factor. 
             
            NOTES AND PRECAUTIONS 
             
                  1.    When sterilizing dilution blanks, a portion of the diluent may be lost.  
                        When this occurs, the sterilized blanks are brought to the proper volume 
                                                                                     3
            Microbiological Methods                                                                                          I-A-  
                                                  
                                                  
                                 MESOPHILIC AEROBIC BACTERIA 
                  (STANDARD PLATE COUNT OR TOTAL PLATE COUNT) ⎯ continued 
                                                  
                                                  
                       with the sterile diluent.  This instruction applies to all methods employing 
                       dilution bottles. 
             
                  2.   The amount of sample to be tested and the extent of dilution is best 
                       determined by each individual laboratory. 
             
                  3.   When running counts on pregelatinized starches, no more than 5 g of 
                       sample per 95 mL of diluent may be used. 
             
                  4.   Plates containing granular samples should be examined with a stereoscopic 
                       microscope to aid in counting small colonies. 
                   
                  5.   The membrane filter technique (I-B) may be used for sugars and syrups if 
                       low counts are anticipated. 
             
            REFERENCES 
             
                  AOAC 2002.07. 
                   
                  Compendium of Methods for the Microbiological Examination of Foods, Third 
                  Edition, 1992, Chapter 4, (http://www.apha.org/media/science.htm). 
             
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...Microbiological methods i a mesophilic aerobic bacteria standard plate count or total principle viable are quantitated by the fractional gram pour technique scope method is applicable to starches syrups and sugars most coproducts of corn wet milling industry media reagents agar pca prepare according manufacturer s directions butterfield phosphate diluent stock solution dissolve g potassium dihydrogen khpo in ml purified water adjust ph with about n naoh dilute l volume store under refrigeration dilution blanks using this fill bottles cap sterilize at c pounds pressure for mins steam autoclave note sodium hydroxide member companies refiners association accepted revised continued procedure two common sample techniques may be used any given number dilutions depends on individual determined past experience factor five series ffs aseptically weigh into sterile blank homogenize primary pdb twenty can transferred another diluted b ten fts same as only etc either pipet each appropriately marke...

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