A biological method for controlling excessive lipid oxidation in salted and dried fish processing
A process and lipid oxidation technology, applied in multi-step food processing, bacteria used in food preparation, food drying, etc., can solve the problems of difficult to control product quality and safety, single product flavor, shortened production cycle, etc. Effects of excessive lipid oxidation, improved nutritional value, and low production cost
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0031] The biological method provided by the present embodiment controls the method for excessive lipid oxidation in the processing process of salted and dried fish, comprising the following steps:
[0032] (1) Raw material processing: select fresh fish, remove the head and viscera, rinse with running water and remove individuals with large differences, and drain;
[0033] (2) Preparation of biological starter: Lactobacillus casei (No. NBRC15883), Leuconostocmesenteroides (No. GIM1.357) and Staphylococcus xylosus were used as fermentation strains. Three generations of activation in the medium (MRS medium composition is: 10.0 grams of casein peptone, 10.0 grams of beef extract, 5.0 grams of yeast extract, 5.0 grams of glucose, 5.0 grams of sodium acetate, 2.0 grams of diamine citrate, 1.0 grams of Tween 80 , 2.0 grams of dipotassium hydrogen phosphate, 0.2 grams of magnesium sulfate heptahydrate, 0.05 grams of manganese sulfate heptahydrate, 20.0 grams of calcium carbonate, and...
Embodiment 2
[0043] The biological method provided by the present embodiment controls the method for excessive lipid oxidation in the processing process of salted and dried fish, comprising the following steps:
[0044] (1) Raw material processing: after natural thawing of frozen fish, remove the head and viscera, rinse with running water and remove the individuals with large differences, and drain;
[0045](2) Preparation of biological starter: Lactobacillus casei, Leuconostocmesenteroides and Staphylococcus xylosus were used as fermentation strains. The strains were respectively activated in MSA medium for three generations, expanded and collected by centrifugation Bacteria were resuspended with sterile saline to prepare 10 8 ~10 9 The fermentation agent of cfu / mL, strain source and specific activation culture process are the same as embodiment 1;
[0046] (3) Inoculation: Inoculate and ferment the fish body with a 6% inoculum amount (V / W) mixed starter, the ratio of the mixed starter ...
Embodiment 3
[0053] (1) Raw material processing: select fresh fish, remove the head and viscera, rinse with running water and remove individuals with large differences, drain and cut into pieces;
[0054] (2) Preparation of biological starter: Lactobacillus casei, Leuconostocmesenteroides, and Staphylococcus xylosus were used as fermentation strains, and the strains were activated in MRS medium for three generations, expanded and collected by centrifugation Bacteria were resuspended with sterile saline to prepare 10 8 ~10 9 cfu / mL starter;
[0055] (3) Inoculation: Inoculate and ferment the fish body with a 7% inoculum (V / W) mixed starter, the ratio of the mixed starter is: Lactobacillus casei: Leuconostoc enterococci: Glucoccus xylosus = 1.5 :1:1, the block fish is inoculated by soaking method, and the soaking time is 40~60min;
[0056] (4) Fermentation and pickling: Put the fish body inoculated with the starter criss-cross into the pickling tank, add 7% salt water until the fish body ...
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More