Microbe starter culture for producing conjugated linoleic acid and preparation method thereof

A microbial starter, conjugated linoleic acid technology, applied in the field of bioengineering, can solve problems such as mild reaction conditions, single isomer composition, and safety doubts

Inactive Publication Date: 2011-11-02
NORTHEAST AGRICULTURAL UNIVERSITY
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the source of CLA is very limited, only in milk and meat products of ruminants, and the content of non-ruminant products is very low
[0003] At present, the industrially produced CLA product is a mixture of multiple isomers, with poor select

Method used

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  • Microbe starter culture for producing conjugated linoleic acid and preparation method thereof

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Embodiment Construction

[0025] Below in conjunction with specific embodiment the present invention is described in more detail:

[0026] Product of the present invention adopts such method to prepare:

[0027] 1. Selection of fermentation strains and preparation of medium

[0028] The present invention selects Lactobacillus plantarum CICC23138, purchased from China Industrial Microorganism Culture Collection Center.

[0029] The basic medium of Lactobacillus plantarum is: peptone 10.0g, beef extract 10.0g, yeast extract 5.0g, glucose 20.0g, anhydrous sodium acetate 5.0g, triamine citrate 2.0g, Tween-801.0mL, dihydrogen phosphate Potassium 2.0g, magnesium sulfate 0.02g, manganese sulfate 0.05g, distilled water 1.0L, pH 6.0-6.5, sterilized at 121°C for 20min.

[0030] 2. The preparation process of starter

[0031] 2.1 Activation of the starting strain

[0032] Measure 0.9% normal saline into 10ml test tubes, sterilize at 121°C for 20 minutes and cool to 30°C, then pour all the freeze-dried bacteria...

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Abstract

The invention provides a microbe starter culture for producing conjugated linoleic acid and a preparation method thereof. The preparation method comprises the following steps that: 1) lactobacillus plantarum CICC 23138 as an original strain is activated through 0.9% of normal saline and is set aside for later use; 2) linoleic acid is added into a lactobacillus plantarum basic medium and the original strain activated in the step 1 is inoculated into the lactobacillus plantarum basic medium, wherein the volume of the added linoleic acid accounts for 0.1% of the volume of the lactobacillus plantarum basic medium and the volume of the added original strain accounts for 5% of the volume of the lactobacillus plantarum basic medium; the inoculated original strain is putted into an anaerobic incubator to be cultured statically for 30 hours at a temperature of 37 DEG C to form cultured bacterial strain as a grade 1 acclimated bacterial strain; linoleic acid is added into a lactobacillus plantarum basic medium and the grade 1 acclimated bacterial strain is inoculated into the lactobacillus plantarum basic medium, wherein the volume of the added linoleic acid accounts for 0.2% of the volume of the lactobacillus plantarum basic medium and the volume of the added grade 1 acclimated bacterial strain accounts for 5% of the volume of the lactobacillus plantarum basic medium; the inoculated grade 1 acclimated bacterial strain is putted into an anaerobic incubator to be cultured statically for 30 hours at a temperature of 37 DEG C to form cultured bacterial strain as a grade 2 acclimated bacterial strain; in the same way, acclimating processes are carried out grade by grade and a grade 7 acclimated bacterial strain is obtained after a grade 7 acclimating process is finished, wherein a low grade acclimated bacterial strain is utilized as an original strain of a higher grade acclimating process and an additive volume of linoleic acid is increased by 0.1% of the volume of a lactobacillus plantarum basic medium; 3) the grade 7 acclimated bacterial strain is cultured in defatted milk and a mature fermented strain is obtained when the defatted milk contains equal to or greater than 1010 living bacteria per milliliter; and 4) the mature fermented strain is treated through the processes of freezing and drying to form culture starter powder.

Description

(1) Technical field [0001] The invention relates to a microbial starter for producing conjugated linoleic acid and a preparation method thereof, in particular to a starter for preparing conjugated linoleic acid by fermenting linoleic acid and a preparation method thereof, belonging to the field of bioengineering. (2) Background technology [0002] Conjugated linoleic acid (CLA) is a class of octadecadienoic acid containing cis- or trans-conjugated double bonds. It is one of the most important functional fatty acids discovered by humans in recent years. CLA has various physiological activities such as anti-cancer, weight loss, anti-atherosclerosis, prevention and treatment of diabetes, regulation of blood lipids, enhancement of body immunity and growth promotion. c9, t11 CLA and t10, c12 CLA are the most physiologically active. However, the source of CLA is very limited, only in milk and meat products of ruminants, and the content of non-ruminant products is very low. [00...

Claims

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Application Information

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IPC IPC(8): C12N1/20C12R1/25
Inventor 侯俊财刘艳平肖志刚于微王玉堂王芳
Owner NORTHEAST AGRICULTURAL UNIVERSITY
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