NZ204748A - Food fermentation process utilising lactic acid producing bacteria - Google Patents

Food fermentation process utilising lactic acid producing bacteria

Info

Publication number
NZ204748A
NZ204748A NZ20474883A NZ20474883A NZ204748A NZ 204748 A NZ204748 A NZ 204748A NZ 20474883 A NZ20474883 A NZ 20474883A NZ 20474883 A NZ20474883 A NZ 20474883A NZ 204748 A NZ204748 A NZ 204748A
Authority
NZ
New Zealand
Prior art keywords
lactobacillus
meat
food
culture
nrrl
Prior art date
Application number
NZ20474883A
Inventor
M Raccach
M A Matrozza
Original Assignee
Microlife Technics
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Microlife Technics filed Critical Microlife Technics
Priority to NZ20474883A priority Critical patent/NZ204748A/en
Publication of NZ204748A publication Critical patent/NZ204748A/en

Links

Landscapes

  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
  • Meat, Egg Or Seafood Products (AREA)

Description

New Zealand Paient Spedficaiion for Paient Number £04748 204748 Priority Date(s): .
Complete Specification Filed: Class: Publication Date: ... M!« P.O. Journal, No: .
NEW ZEALAND PATENTS ACT, 1953 No.: Date: COMPLETE SPECIFICATION FERMENTATION METHOD USING A SELECTED LACTOBACILLUS 3c/We, MICROLIFE TECHNICS, INC. a corporation of Delaware, United States of America, of 1833 57th Street, Sarasota, Florida 33578, United States of America hereby declare the invention for which we pray that a patent may be granted to ngft^us, and the method by which it is to be performed, to be particularly described in and by the following statement: - - 1 - (followed by page la) 204748 (q_ FERMENTATION METHOD U3ING A GELECTED LACTOBACILLUS BACKGROUND OF THE INVENTION The present invention relates to a method for fermenting foods using selected cultures of a lactobacillus having the rapid low temperature fermentation characteristics of Lactobacillus casei NRRL-B-15,438 usually "at food temperatures of between 15.6°C (60°F) and 26.7°C (80°F) in the presence of an effective amount of a stimulatory, food grade metal salt, preferably a manganese salt. Fermentation temperatures in the range between about 15.6°C (60°F) and 48.9°C (120°F) can be used; however, lower temperatures than 26.7°C (80°F) are preferred, particularly to reduce the risk of significant Staphylococcus aureus growth in fermented meats.
Prior Art The prior art has generally described meat fermentation methods using many different cultures of lactobacilli which generate lactic acid from dextrose, lactose, glycogen, sucrose and/or starch in foods. U.S. Patent Nos. 2,225,783 and 3,193,391 to Jensen et al; 3,098,744 to Von Lorch et al; 3,814,817 to Everson et al and 3,561,977 and 3,910,664 to Rothchild et al are representative of this prior art which is extensive. In this prior art, various strains of lactobacilli are described as useful for fermenting foods; however, these cultures have the characteristic of fermenting lactose, starch and glycogen which, when present in uncontrolled or unknown amounts in a meat mixture to be fermented, can result in the production of excessive amounts of lactic acid causing an undesirable low final pH in the fermented meat. fc&Wf - 2 0 4- / 4 B It is generally true of lactobacilli and specifically most strains of Lactobacillus casei that sausage fermentations proceed very slowly or not at all at temperatures less than 26.7°C (80°F). Commercially meat 5 fermentations are usually conducted above 26.7°C (80°F) for this reason.
Usually semi-dry sausage is prepared by fermenting a carbohydrate particularly dextrose and/or naturally occurring glycogen in meat in less than about 30 10 hours. Dry sausage is usually fermented over a period of at least two to three days. Both methods preferably involve a rapid initial fermentation which produces lactic acid in the meat thereby lowering the pH. Once the pH is • lowered to the desired level any further lowering of the pH 15 makes the product unacceptable. This can particularly occur during the drying period required to make dry sausage.
In general, the prior art strains of lactobacilli used for making sausage to develop a pH of 20 less than about 5.0 in about 30 hours or less, require fermentation at an elevated temperature range between about 26.6 °C to 45°C (80 °F to 113°F). These lactobacilli are too slow at lower meat temperatures between about 10°C to 26.7° (50°F to 80°F) since they take much longer to develop a pH 25 of less than about 5.0.
In U.S. patent No. 4,303,67 9 the use of manganese salts in the fermentation of meats using specific unique strains of Pediococcus pentosaceus is described. U.S patent No. .2,945,766 to Chiat generally describes the 30 use of manganese salts in meat fermentations with lactobacilli at temperatures at or above 26.7°C (80°F).
Hanna, M. 0., et al Journal of Food Protection Vol 43 pages 837-841' describe the use of Lactobacillus casei subspecies alactosus in vacuum packed meat at 1 to 35 3°c for preservation without fermentation. These cultures were not effective and detracted from the taste of the meat. 20474$ .... -3- Objects It is therefore an object of the present invention to provide a method for producing fermented foods using selected cultures of ——: Lactobacillus casei NRRL—B—15,438 with a stimulatory metal salt which cultures ferment rapidly at low temperatures. It is particularly an object of the present invention to provide a method wherein fermented meats can be produced using Lactobacillus casei — NRRL-B-15,438 and stimulatory metal salt wherein the meat mixture to be fermented contains unknown or uncontrolled amounts of certain carbohydrates. These and other objects will become increasingly apparent from the following description.
General Description The present invention relates to the improvement in a food fermentation method including the steps of providing lactic acid producing bacteria in the food with an assimilable carbohydrate and then fermenting the food with the bacteria so that lactic acid is produced from the carbohydrate over a period of time in the food which comprises: providing in admixture in a food a culture of a lactobacillus with an assimilable carbohydrate and with a stimulatory, food grade metal salt in an amount sufficient to accelerate the fermentation by the lactobacillus, wherein the culture is characterized by having low temperature fermentation characteristics in food at least as rapid as Lactobacillus casei NRRL-B-15,438; and fermenting the food admixture at temperatures between about 15.6°C and 48.9°C so that lactic acid is produced in the food product. Using Lactobacillus casei NRRL-B-15,438 at a concentration of 3.6 x 10^ cells per grams of meat, a pH of 204748 .0 usually can be achieved at 24°C in less than about 2 4 hours with an initial food pH of about 5.9 without the metal salt. With the metal salt, the fermentation time is significantly decreased under equivalent conditions.
The present invention particularly relates to the meat fermentation method including the steps of providing lactic acid producing bacteria in the meat with an assimilable sugar and then fermenting the meat with the bacteria so that lactic acid is produced from the sugar over a period of time in the fermented meat wherein the improvement comprises: providing in admixture in meat a culture of a lactobacillus having low temperature meat fermentation characteristics at least as rapid as Lactobacillus casei NRRL-B-15,438 at a concentration of between about 105 and 109 of the lactobacillus per gram of meat with an assimilable carbohydrate and with a stimulatory food grade manganese salt in an amount sufficient to stimulate the growth of the lactobacillus wherein the lactobacillus culture is characterized by an ability to rapidly ferment in the meat admixture at meat temperatures of about 24°C to produce a pH of about 5 or less; and fermenting the meat admixture at smokehouse temperatures between about 15.6°C and 48.9°C so that lactic acid is produced in the fermented meat product.
The present invention further relates to a culture of lactobacillus adapted for meat fermentations including an assimilable carbohydrate at smokehouse temperatures between about 15.6°C and 48.9°C which comprises a selected lactobacillus grown in growth medium including assimilable sources of carbon, nitrogen and inorganic substances to a concentration of at least about 1 x 10*7 of the lactobacillus per ml, having a pH between about 4 and 8 and containing a stimulatory food grade metal salt after growth in an amount sufficient to accelerate the fermentation in the meat by providing a concentration of ;? A r'pr. ;■' i % ;204748 ;-5- ;metal ion between about 0.01 ppm and 1500 ppm in the meat, wherein the selected lactobacillus culture is characterized by an ability to rapidly ferment in a meat admixture with an assimilable sugar at temperatures of about 2 4°C to produce a pH less than about 5 at least as rapidly as Lactobacillus casei NRRL-B-15,438. ;By a process which involves selective testing or genetic manipulation, lactobacillus having similar low temperature fermentation characteristics can be found or produced. Examples 1 and 2 show Lactobacillus casei subspecies alactosus NRRL-B-12,344. Examples 5, 6 and 7 show Lactobacillus casei NRRL-B-15,438. In some instances the selected lactobacillus may not be of the same strain or the same species. All of this is well known to those skilled in the art. ;The lactobacillus cells can be used as a concentrate having a pH between about 4 and 8 containing at least about 1 x 10' cells per gram up to about 10^-5 cells per gram, usually between about 1 x 109 and 10^2 cells per gram, mixed with the stimulatory metal salt, preferably a manganese salt. The concentrates are prepared by centrifugation by reverse osmosis, by ultrafiltration, or by dialysis of the cells in the growth medium, all of which are well known to those skilled in the art. The concentrates containing the stimulatory metal salt can be frozen with or without a freezing stabilizing agent such as monosodium glutamate, malt extract, non-fat dry milk, ;alkali metal glycerophosphate, glutamic acid, cystine, glycerol, or dextran or the like and then thawed for use or the concentrates can be lyophilized to a powder as is well known to those skilled in the art. The bacterial cells are used in a range between about 10^ to 10^ cells per gram of meat. ;The stimulatory metal salt is used in an amount of metal cation in the salt above about 0.01 parts per ;2 0474 ;-6- ;million to about 1500 parts per million by weight of the food to be fermented, preferably between about 0.1 and 100 ppm. The metal salt must be food grade. Such salts include for instance: manganese chloride, manganese sulfate, manganese citrate, manganese glycerophosphate, manganese oxide and manganese gluconate and various non-toxic metal salts of acids which are at least slightly soluble in water. Other metal salts include ferrous, ferric, magnesium, calcium, zinc salts; however, none are as effective as manganese. The metal salt can be incorporated into the bacterial culture in an amount between about 0.01 and 50 percent by weight of the culture in order to provide the required amount of the metal salt needed in the food when the culture is added. ;The low temperature lactobacillus, particularly Lactobacillus casei NRRL-B-12,344 or Lactobacillus casei NRRL-B-15,4 38, admixed with the stimulatory metal salt causes nitrite reduction due to the lowering of the pH of the meat in fermented meats, particularly pork including bacon and ham at a pH of between about 5 and 6 and at a concentration of bacteria between about 10^ and 10^-0 cells per ml. Usually the bacteria are included in the aqueous pickling solution and added to the meat as a spray or injected in an amount up to 15% by weight of the meat. ;Bacon is usually not reduced to a pH less than about 6 from an initial pH of 6.3 to 6.4. The lactobacillus with a stimulatory metal salt can lower the pH thus causing the nitrite reduction at lower temperatures than can be achieved in the absence of the stimulatory metal salt. Specific Description ;The Lactobacillus casei subsp. alactosus strain of the present invention has been deposited at the Northern Regional Research Laboratory of the USDA, Peoria, Illinois and was designated as NRRL-B-12,344. NRRL-B-12,344 or a lactobacillus which has substantially the same low temperature meat fermentation characteristics is used in ;20474 8 ;-7- ;the present invention. The essential identification characteristics of this strain and related strains are shown in Table I. ;2 04748 ;10 ;15 ;20 ;25 ;30 ;-8- ;Table I ;Carbohydrate Fermentation Pattern ;Substrate ;Adonitol ;Arabinose ;Cellobiose ;Dextrose ;Culcitol ;Galactose ;Glycerol ;Inositol ;Lactose ;Maltose ;Mannitol ;Mannose ;Melibiose ;Nitrate reductase ;ONPG ;Raffinose ;Rhamnose ;Salicin ;Sorbitol ;Sucrose ;Trehalose ;Xylose ;Starch ;Esculin ;Levulose ;Amygdalin ;Fructose ;Gluconate ;Glycogen ;Ribose ;Catalase ;Fermentation Reaction ;Negative ;Negative ;Negative ;Positive ;Negative ;Positive ;Negative ;Negative ;Negative ;Positive ;Negative ;Positive ;Negative ;Negative ;Negative ;Negative ;Negative ;Negative ;Weak + ;Positive ;Negative ;Negative ;Negative ;Negative ;Positive ;Weak ± ;Positive ;Positive ;Negative ;Positive ;Negative ;35 ;There is growth at 17°C, 24°C, 35°C and no growth at 45°C. NRRL-B-12,344 produces primarily L (+) ;lactic acid. Acid but no gas from glucose. Acid and gas are produced from gluconate. Lactobacillus casei subspecies alactosus has been used without a stimulatory metal salt at elevated temperatures above 26.7°C (80°F) in mixed bacterial cultures with other lactic acid producing bacteria which broadly ferment most carbohydrates. ;Example 1 ;The preparation of a bacterial concentrate is described in this Example. Lactobacillus casei subspecies alactosus NRRL-B-12,344 was grown in a growth medium such as described in U.S. Patent Nos. 3,561,977 and 3,960,664. The medium includes a carbohydrate (glucose or other assimilable sugar) a nitrogen source (yeast extract or other source of amino acids) and traces of essential minerals or inorganic substances usually including a manganese salt (manganese sulfate monohydrate). The pH of the medium was initially adjusted to between 6.5 to 6.7 and the fermenter was set to maintain a pH of 6.0 during growth by the intermittent addition of ammonia. NRRL-B-12,344 was grown at 35°C for about 15 hours. The bacteria were then concentrated using a centrifuge and, where the concentrate was not to be used immediately, were mixed with glycerin as a freezing stabilizing agent (10% by weight) and frozen for storage. The concentrates were also mixed with the manganese sulfate monohydrate as indicated in the following Examples prior to freezing. ;Example 2 ;The Lactobacillus casei subspecies alactosus NRRL-B-12,34 4 culture of Example 1 prior to centrifugation contained 8 x 10^ cells per milliliter in the growth medium. The culture was centrifuged and then resuspended at the rate of 5 milliliters of supernatant liquid per 100 ml of original culture. One milliliter ( 1 ml) of this concentrate was diluted with 20.3 milliliters of tap water and was inoculated at a rate of 4.5 milliliters of diluted culture per 0.93 kg (2.5 pounds) of sausage mix (40% pork ;2 04748 ;-10- ;and 60% beef with 3.0% salt, 1.0% dextrose, spices and 0.0156% sodium nitrite) which supplied about 3 x 10? cells per gram of the sausage mix. Lactobacillus casei subspecies alactosus NRRL-B-12,344 was tested with no metal ion, with calcium chloride and with manganese sulfate monohydrate in an amount of 13 parts per million of the metal cation based upon the weight of the sausage. ;Procedure ;1) The meat was comminuted to the selected size. ;2) The dextrose, salt, spice mix, metal salt and sodium nitrite were added to the comminuted meat and mixed. ;3) The sausage mix was divided into aliquots and inoculated with appropriate cultures and mixed thoroughly. ;4) The sausage mix was stuffed into 53 mm diameter fibrous casings using a hydraulic stuffer. ;5) The sausages were fermented at 2 4°C (75.2°F) dry bulb and 21°C (69.8°F) wet bulb (80% ;room humidity) using a controlled environment chamber. ;Determination of pH ;1) The pH of the sausage was determined at various times. ;2) Thirty grams of sausage were blended with 90 ml distilled water for 30 to 60 seconds. The pH of the slurry was determined. Prior to each pH reading, the pH meter was calibrated against two standard buffers (pH values of 7.00 and 4.01). ;Results ;Treatment ;Lactobacillus 5 casei subsp. ;alactosus ;NRRL-B-12,344 0 13 15 17 18 19 20 22 23 Control ;(no additive) 5.87 5.59 5.52 5.35 — 5.19 5.13 5.06 ;10 Ca chloride 5.81 5.56 5.44 5.29 — — 5.17 5.10 5.01 Mn sulfate monohydrate 5.86 5.51 5.29 5.15 5.06 4.97 — — — ;Thus Lactobacillus casei subsp. alactosus NRRL-B-12,344 achieved a pH of less than 5.0 in less than 15 19 hours with the manganese salt as compared to more than 23 hours for the control. At this level, it cannot be said that calcium is significantly stimulatory. ;Comparative Example 3 Example 2 was repeated at 13 ppm metal ion 20 concentration except that Lactobacillus lactis, Parr ;(NRRL-B-5628) and Lactobacillus plantarum (NRRL-B-5461) as described in U.S. Patent Nos. 3,984,575 and 3,814,817 were used at 24°C (75 2°F). The results are shown in Table III. ;' 2 0-4748 ;-11- ;Table II Fermentation Period (Hours) ;25 ;2 04748 ;-12-Table III ;Treatment Fermentation Period (Hours) ' ;Lactobacillus plantarum ;NRRL-B-5461 JO 21 24 27 29 34 38 45 48 51 ;(pH values) ;Control ;(no additive) 5.80 5.62 5.53 5.20 5.11 — — — ;CaCl2 5.19 5.65 5.51 5.24 5.13 — — — ;MnSC>4 monohydrate 5.77 5.56 5.33 5.00 — -— — — ;Lactobacillus lactis Farr NRRL-B-5628 ;Control ;(no additive) 5.86 5.79 5.72 5.73 -- 5.59 5.39 5.20 5.19 5.15 ;CaCl2 5.81 5.80 5.75 5.73 -- 5.58 5.35 5.23 5.16 5.15 MnS04 ;Monohydrate 5.88 5.80 5.80 5.77 ~ 5.48 5.24 5.03 ' — ;Comparative Example 4 Example 2 was repeated with Lactobacillus casei NRRL-B-12428, which has higher temperature fermentation characteristics, at the level of 3 x 10*7 cells per gram of sausage and at 24°C (75.2°F). The result was that the fermentation was very long (40 hours) and there appeared to be only a slight improved result over the control. The results are shown in Table IV where pH is shown as a function of time. 2 047 4 8 Table IV Treatment Fermentation Period (Hours) Initial 16 19 , 23 25 40 44 Control (no additive) 5.76 5.67 5.69 5.52 5.56 5.16 4.98 CaCl2 5.76 5.65 5.65 5.64 5.61 5.16 4.99 MnSC>4 monohydrate 5.75 5.71 5.67 5.63 5.59 4.84 — Final Viable Counts Control 36 x 107 MnS04 monohydrate 40 x 107 CaCl2 34 x 107 Comparative Example 4 shows the metal salts are only selectively stimulatory at low temperatures even with certain strains of Lactobacillus casei.
The preferred selected Lactobacillus casei strain of the present invention has been deposited at the Northern Regional Research Laboratory of the USDA, Peoria, Illinois and was designated as NRRL-B-15,438. The essential identification characteristics of this strain are shown in Table V. 204748 -14-TABLE V Carbohydrate Fermentation Pattern Substrate Fermentation Reacl Adonitol Negative Arabinose Negative Cellobiose Negative Dextrose Positive Dulcitol Negative Galactose Slow Positive Glycerol Negative Inositol Negative Lactose Positive Maltose Negative Mannitol Negative Mannose Positive Melibiose Negative Nitrate reductase Negative ONPG Negative Raffinose Negative Rhamnose Negative Salicin Negative Sorbitol Negative Sucrose Positive Trehalose Positive Xylose Negative Starch Negative Esculin Negative Levulose Negative Axnygdalin Weak ± Ribose Positive Catalase Negative Growth at 17°C, 24 °C, 35°C and no 45°C. 2 04748 -15-Example 5 The preparation of a frozen concentrate of NRRL-B-15,438 was described in a laboratory fermentor as described in Example 1. The sausage mixture and procedure were as described in Exanple 2, except that only pork was used for the sausage meat mixture.
The meat mixture was inoculated at a rate to deliver 1-8 x 107 NRRL-B-15,438 cells per gram of the sausage mix. Lactobacillus casei NRRL-B-15,438 was tested with no metal ion and with manganese sulfate monohydrate in an amount of 4 parts per million of the metal cation based upon the weight of the sausage.
The sausage mix was stuffed into 44 mm diameter fibrous casings using a hydraulic stuffer.
The sausage were fermented at 24°C (75.2°F) wet bulb and 25°C (77°F) dry bulb (92% relative humidity) using a controlled environment chamber.
Results The results are shown in Table VI.
Table vi'(l> (pH) Treatment Fermentation Period (Hours) Lactobacillus casei NRRL-B-15,438 _0 13 16 19 21 Control (no additive) 5.98 5.88 5.68 5.50 5.35 Mn sulfate monohydrate 5.98 5.80 5.52 5.25 5.12 (l^The initial concentration of cells was half the usual inoculum as shown in Example 2. Thus, usually 3.6 x 107 cells per gram of meat is the inoculation rate. The data in Table VI is with an inoculation rate of 1.8 x 107 cells per gram of meat. It is still relatively fast at lower temperatures. 204748 Example 6 Sausages were prepared as in Example 5 and were inoculated with production fermenter produced Lactobacillus casei NRRL-B-15,438 or with a commercial preparation of . Pediococcus pentosaceus NRRL-B-11,465 to compare fermentation speed and color development at 24°C (75.2°F) wet bulb temperature. Both sausages contained manganese sulfate monohydrate in an amount of 4 parts per million of the metal cation based on the weight of the sausage.
Pediococcus NRRL-B-11,465 was added at a rate to deliver 3.6 x 107 cells per gram of meat and Lactobacillus casei NRRL-B-15,438 was added at a rate to deliver 1.8 x 107 cells per gram of meat.
Sausages were incubated at temperatures as described in Example 5.
Results The results are shown in Table VII.
Table VII (Fermentation Period in Hours) 0 15.75 17 19.5 21.25 24.25 Treatment pH Color pH Color pH Color pH Color pH Color pH Color Pediococcus NRRL-B-11465 5.86 0 5.69 0 5.61 0 5.59 0 5.45-3+ 5.24 4+ .
Lactobacillus casei NRRL-B-15438 5.86 0 5.04 5+ 4.98 5+ - - - - Color 0 = No color development + = Full red color development 204748 The results indicate that Lactobacillus casei NRRL-B-15,438 is superior in producing cured meat color and is much faster than Pediococccus NRRL-B-11,465 in acid production in sausage fermented at 24°C even though half as 5 many cells were used.
Example 7 A concentrate of Lactobacillus casei NRRL-B-15,438 was prepared as described in Example 5 and was lyophilized using procedures well known to those skilled in the art. Sausages were made as described in Example 5 except lyophilized cells of Lactobacillus casei NRRL-B-15,438 were added at a rate to deliver 1 x 107 viable Lactobacillus casei NRRL-B-15,438 cells per gram of meat.
The sausages were incubated as described in Example 5.
Results The results are shown in Table VIII.
Table VIII.
Treatment Fermentation Period (Hours) Lyophilized Lactobacillus casei NRRL-B-15,438 0 21 24 26.25 28.5 30.5 Control (No MnS04 monohydrate) 5.9 5.76 5.58 5.46 5.37 5.32 MnS04 monohydrate 5.9 5.67 5.42 5.24 5.07 4.95 The results in Table VIII show that lyophilized cells of Lactobacillus casei NRRL-B-15,438 also are stimulated by manganese ion at 24°C.
Lactobacillus species having low temperature fermentation characteristics at as rapid as Lactobacillus 35 casei subspecies alactosus NRRL-B-12,344 with a stimulatory metal salt provides a significantly improved method for fermenting foods, vegetables and meats. Lactobacillus

Claims (7)

    204748 -19- casei NRRL-B-15,438 is particularly preferred because of the rapid red color development. 204748 -20- WHAT J^'WH CLAIM IS: -
  1. l- The improvement in a food fermentation method including the steps of providing lactic acid producing bacteria in the food with an assimilable carbohydrate and then fermenting the food with the bacteria so that lactic acid is produced from the carbohydrate over a period of time in the food which comprises: (a) providing in admixture in a food a culture of a lactobacillus with an assimilable carbohydrate and with a stimulatory, food grade metal salt in an amount sufficient to accelerate the fermentation by the lactobacillus, wherein the culture is characterized by having low temperature fermentation characteristics in food at least as rapid as Lactobacillus casei NRRL-B-15,438; and (b) fermenting the food admixture at temperatures between 15.6°C and 4 8.9°C so that lactic acid is produced in the food product. -2- In a meat fermentation method including the steps of providing lactic acid producing bacteria in the meat with an assimilable sugar and then fermenting the meat with the bacteria so that lactic acid is produced from the sugar over a period of time in the fermented meat the improvement which comprises: (a) providing in admixture in meat a culture of a selected lactobacillus having low temperature meat fermentation characteristics at least as rapid as Latobacillus casei NRRL-B-15,438 at a concentration of between 105 and 109 of the selected lactobacillus per gram of meat with an assimilable carbohydrate and with a stimulatory, food grade manganese salt in an amount -■ sufficient to stimulate the growth of the lactobacillus, wherein the lactobacillus culture is characterized by an ability to rapidly ferment in the meat admixture at^meat temperatures of about 24°C to produce a pH of 5 .or v A' e4 V. ' ,A V less; and ^ c % / y £ o ^ ' 204748 (b) fermenting the meat admixture at smokehouse temperatures between 15.6°C and 49.9°C so that lactic acid is produced in the fermented meat product. -3- The method of Claim 2 wherein the meat admixture contains a food grade nitrite as a preservative which is partially reduced due to the lactic acid produced by the lactobacillus. -4- The method of Claim 2 wherein the lactobacillus, sugar, preservatives and metal salt are added to the meat as an aqueous pickling solution containing between 10$ to 10^0 of the lactobacillus per ml in an amount of the pickling solution up to 15 percent by weight based upon the meat weight and wherein the meat is held at 21.1°C to 38 °C until a pH between 5 and 6 is achieved. -5- The method of Claim 1 or 2 wherein the metal salt is manganese sulfate and wherein the food is fermented at temperatures of 26.7°C or less to produce a pH of less-than 5. -6- The method of Claim 1 or 2 wherein the lactobacillus has essentially the same meat fermentation characteristics as Lactobacillus casei NRRL-B-15,438. -7- The method of Claim 1 or 2 wherein the lactobacillus is Lactobacillus casei NRRL-B-15,438.
  2. 2-04748 -22- -8- The method of Claim 1 or 2 wherein the lactobacillus has been grown in the presence of a manganese salt and further manganese salt is added to the culture as the metal salt after growth .and wherein the lactobacillus is admixed with the food as a liquid concentrate containing at least 107 cells per gram. -9- The method of Claim 8 wherein the bacterial concentrate is frozen with the manganese salt prior to use and thawed to provide a liquid concentrate for admixture with the food. -10- The method of Claim 1 or 2 wherein the lactobacillus is in a lyophilized, powdered form containing the metal salt which is provided in the food as a powder. \ -11- The method of Claim 1 wherein portions of fermented food are utilized as a source of lactobacillus for a subsequent food fermentation with the metal salt. -2
  3. 3- % 04748 -12- A culture of a lactobacillus adapted for meat fermentations including an assimilable carbohydrate at smokehouse temperatures between 15.6°C and 48.9°C which comprises.a selected lactobacillus grown in growth medium including assimilable sources of carbon, nitrogen and .inorganic substances to a concentration of at least 1 x 107 of the lactobacillus per ml, having a pH between 4 and 8 and containing a stimulatory food grade metal salt after growth in an amount sufficient to accelerate the fermentation in the meat by providing a concentration of metal ion between 0.01 ppm and 1500 ppm in the meat, wherein the selected lactobacillus culture is characterized'by an ability to rapidly ferment in a meat admixture with an assimilable sugar at temperatures of about 24°C to produce a pH less than .5,.at least as rapidly as Lactobacillus casei NRRL-B-15,438. -13- The culture of Claim 12 wherein the lactobacillus has essentially the identification characteristics of Lactobacillus casei ■ NRRL-B-15,438 and has been grown in the presence of a manganese salt as the metal salt. -1
  4. 4- - The culture of Claim 12 wherein the lactobacillus is Lactobacillus casei NRRL-B-15,438. -1
  5. 5- The culture of Claim 12 containing between 10^ and 10^2 0f the lactobacillus per gram and a manganese salt as the metal salt. 204748 -24- -1
  6. 6- The culture of Claim 12 wherein the growth medium contains a manganese salt, in an amount sufficient to facilitate the growth of the cells in the medium. -1
  7. 7- The culture of Claim 12 wherein the metal salt is a manganese salt. rp DATED THIS DAY OF P- U: A. J. PARK & SON AGENTS FOR THE APPLICANTS
NZ20474883A 1983-06-29 1983-06-29 Food fermentation process utilising lactic acid producing bacteria NZ204748A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
NZ20474883A NZ204748A (en) 1983-06-29 1983-06-29 Food fermentation process utilising lactic acid producing bacteria

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
NZ20474883A NZ204748A (en) 1983-06-29 1983-06-29 Food fermentation process utilising lactic acid producing bacteria

Publications (1)

Publication Number Publication Date
NZ204748A true NZ204748A (en) 1986-03-14

Family

ID=19920404

Family Applications (1)

Application Number Title Priority Date Filing Date
NZ20474883A NZ204748A (en) 1983-06-29 1983-06-29 Food fermentation process utilising lactic acid producing bacteria

Country Status (1)

Country Link
NZ (1) NZ204748A (en)

Similar Documents

Publication Publication Date Title
US4013797A (en) Bacterial compositions and process for fermentation of meat therewith
Berry et al. The use of bacteriocin-producing Pediococcus acidilactici to control postprocessing Listeria monocytogenes contamination of frankfurters
Shelef et al. Growth suppression of Listeria monocytogenes by lactates in broth, chicken, and beef
Raccach Pediococci and biotechnology
US4147807A (en) Process for the treatment of meat with compositions including Micrococcus varians and a lactic acid producing bacteria
JP4243442B2 (en) Method for producing fermented seafood
Deibel et al. Microbiology of meat curing: IV. A lyophilized Pediococcus cerevisiae starter culture for fermented sausage
US4304868A (en) Process for the treatment of meat with compositions including Micrococcus varians and a lactic acid producing bacteria
EP0943247A1 (en) Method and compositions for improved flavor and aroma in fermented meat
US2225783A (en) Sausage treatment
Coventry et al. Growth characteristics of meat starter cultures
US4579740A (en) Fermentation method using a selected lactobacillus
EP0130228A1 (en) Fermentation method using a selected lactobacillus
Harmayani et al. Fate of Listeria monocytogenes in raw and cooked ground beef with meat processing additives
US3814817A (en) Process for curing dry and semi-dry sausages
US4514424A (en) Fermentation composition using a selected lactobacillus
EP0253158A2 (en) Method for developing a red color in cured meat
US4407828A (en) Fermentation method using a selected lactobacillus
Kearney et al. Meat fermentations with immobilized lactic acid bacteria
US4521434A (en) Fermentation method and compositions including a lactobacillus species strain
Deibel et al. Microbiology of meat curing: I. The occurrence and significance of a motile microorganism of the genus Lactobacillus in ham curing brines
US4917906A (en) Process for preserving raw meat with a bacteria-lysing enzyme from streptomycetes
JP2879261B2 (en) Production method of processed meat products
NZ204748A (en) Food fermentation process utilising lactic acid producing bacteria
Raccach et al. Effect of manganese ions on the fermentative activity of frozen‐thawed lactobacilli