CN106190926A - A kind of enterococcus faecalis fermentation medium - Google Patents
A kind of enterococcus faecalis fermentation medium Download PDFInfo
- Publication number
- CN106190926A CN106190926A CN201610760483.4A CN201610760483A CN106190926A CN 106190926 A CN106190926 A CN 106190926A CN 201610760483 A CN201610760483 A CN 201610760483A CN 106190926 A CN106190926 A CN 106190926A
- Authority
- CN
- China
- Prior art keywords
- enterococcus faecalis
- fermentation medium
- nitrogen source
- peptone
- sucrose
- Prior art date
- Legal status (The legal status 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 status listed.)
- Pending
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N1/00—Microorganisms, e.g. protozoa; Compositions thereof; Processes of propagating, maintaining or preserving microorganisms or compositions thereof; Processes of preparing or isolating a composition containing a microorganism; Culture media therefor
- C12N1/20—Bacteria; Culture media therefor
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Genetics & Genomics (AREA)
- Organic Chemistry (AREA)
- Zoology (AREA)
- Biotechnology (AREA)
- Wood Science & Technology (AREA)
- Microbiology (AREA)
- Medicinal Chemistry (AREA)
- Biomedical Technology (AREA)
- Virology (AREA)
- Biochemistry (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Tropical Medicine & Parasitology (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
Abstract
The present invention relates to a kind of enterococcus faecalis fermentation medium, it is made up of the component of following mass percent: sucrose 1% 5%, peptone 0.5% 2%, biological nitrogen source 1% 5%, potassium dihydrogen phosphate 0.01% 0.1%, dipotassium hydrogen phosphate 0.1% 1%, magnesium sulfate 0.1% 1%, manganese sulfate 0.001% 0.005%, surplus is water.This culture medium achieves the low cost as microbial ecological agent enterococcus faecalis, high efficiency production.
Description
Technical field
The invention belongs to technical field of bioengineering, be specifically related to a kind of enterococcus faecalis fermentation medium.
Background technology
Enterococcus faecalis (Enterococcus Faecium) belongs to the normal flora in people and animal intestinal, after entering intestinal
Can the most surely grow.Enterococcus faecalis fermentation produces lactic acid, advantageously reduces intestinal environment pH, the growth of suppression harmful bacteria.Dung intestinal ball
Bacterium metabolic process also can produce the materials such as hydrogen peroxide, bacteriocin, pathogenic bacterium are had certain killing action, and does not occurs
Medicine is residual.In view of the above characteristic of enterococcus faecalis, increasing producer selects it to carry out the fermenting and producing of microbial ecological agent.
Traditional lactic acid bacteria fermentation many selections MRS culture medium, expensive, the viable count after fermentation is less than 1 × 10 9
CFU/mL, in the case of the effective using dosage of probiotic bacteria is fixing, low fermentation level adds cost equal to covert.Low cost
Culture medium, the fermentation technology that can amplify efficiently for advance probiotics fermention industrialization have great guidance and practice meaning
Justice.
Summary of the invention
It is an object of the invention to provide a kind of enterococcus faecalis fermentation medium, this culture medium achieves as Tiny ecosystem system
The low cost of agent enterococcus faecalis, high efficiency production.
For achieving the above object, the technical solution used in the present invention is as follows:
The invention provides a kind of enterococcus faecalis fermentation medium, it is made up of the component of following mass percent: sucrose 1%-
5%, peptone 0.5%-2%, biological nitrogen source 1%-5%, potassium dihydrogen phosphate 0.01%-0.1%, dipotassium hydrogen phosphate 0.1%-1%, magnesium sulfate
0.1%-1%, manganese sulfate 0.001%-0.005%, surplus is water.
According to above-mentioned enterococcus faecalis fermentation medium, it is made up of the component of following mass percent: sucrose 1%-
3%, peptone 1.5%-2%, biological nitrogen source 1%-3%, potassium dihydrogen phosphate 0.01%-0.04%, dipotassium hydrogen phosphate 0.6%-1%, magnesium sulfate
0.4%-1%, manganese sulfate 0.004%-0.005%, surplus is water.
Enterococcus faecalis fermentation medium according to claim 1, it is made up of the component of following mass percent:
Sucrose 3.1%-5%, peptone 0.5%-1.4%, biological nitrogen source 3.1%-5%, potassium dihydrogen phosphate 0.05%-0.1%, dipotassium hydrogen phosphate
0.1%-0.55%, magnesium sulfate 0.1%-0.35%, manganese sulfate 0.001%-0.003%, surplus is water.
According to above-mentioned enterococcus faecalis fermentation medium, it is made up of the component of following mass percent: sucrose 3%, egg
White peptone 1%, biological nitrogen source 2%, potassium dihydrogen phosphate 0.05%, dipotassium hydrogen phosphate 0.5%, magnesium sulfate 0.5%, manganese sulfate 0.002%, surplus
For water.
According to above-mentioned enterococcus faecalis fermentation medium, described biological nitrogen source is mainly by aminoacid, vitamin and mineral
Composition.
According to above-mentioned enterococcus faecalis fermentation medium, in the composition in described biological nitrogen source, dry is more than 70%, and total nitrogen is big
In 8%, amino-acid nitrogen is more than 2%, and ash is less than 15%, pH value 5.0-6.5.
Compared with prior art, beneficial effects of the present invention:
Culture medium of the present invention contains biological nitrogen source, it is possible to accelerates enterococcus faecalis and rapidly enters exponential phase, fermentation liquid viable count
Averagely can improve more than 30%.Fermentation period can be made to shorten 2-3 hour, thus reduce production cost.
Detailed description of the invention
Following example are intended to further illustrate present disclosure, but are not intended to protection scope of the present invention.
Following raw material sucrose, peptone, biological nitrogen source, potassium dihydrogen phosphate, dipotassium hydrogen phosphate, magnesium sulfate and manganese sulfate are
Commercially available;The producer in biological nitrogen source be Xuzhou City be a day Science and Technology Ltd..
Embodiment 1
A kind of enterococcus faecalis fermentation medium, it is made up of the component of following mass percent: sucrose 1%-5%, peptone
0.5%-2%, biological nitrogen source 1%-5%, potassium dihydrogen phosphate 0.01%-0.1%, dipotassium hydrogen phosphate 0.1%-1%, magnesium sulfate 0.1%-1%, sulfur
Acid manganese 0.001%-0.005%, surplus is water.
Enterococcus faecalis is inoculated in the culture medium of inventive formulation the process conditions carrying out fermenting: fermentation temperature 36-37
DEG C, micro-ventilation maintains tank pressure 0.03-0.04MPa, speed of agitator 80-100 rev/min, PH5.0-6.5, fermentation period 12 hours, can
Obtain more than enterococcus faecalis fermentation liquid viable bacteria 15,000,000,000/milliliter.
Use conventional fermentation technology in the fermentation cylinder for fermentation of 500L, be up to 100 with plate dilution assay method viable count
Hundred million cfu/ml, ferment 14-16 hour.
Embodiment 2
A kind of enterococcus faecalis fermentation medium, it is made up of the component of following mass percent: sucrose 3%, peptone 1%, raw
Thing nitrogen source 2%, potassium dihydrogen phosphate 0.05%, dipotassium hydrogen phosphate 0.5%, magnesium sulfate 0.5%, manganese sulfate 0.002%, surplus is water.
The technological condition for fermentation of the present embodiment is same as in Example 1.
Embodiment 3
A kind of enterococcus faecalis fermentation medium, it is made up of the component of following mass percent: sucrose 1%, peptone 2%, raw
Thing nitrogen source 1%, potassium dihydrogen phosphate 0.1%, dipotassium hydrogen phosphate 0.1%, magnesium sulfate 1%, manganese sulfate 0.001%, surplus is water.
The technological condition for fermentation of the present embodiment is same as in Example 1.
Embodiment 4
A kind of enterococcus faecalis fermentation medium, it is made up of the component of following mass percent: sucrose 2%, peptone 1.8%,
Biological nitrogen source 2%, potassium dihydrogen phosphate 0.08%, dipotassium hydrogen phosphate 0.2%, magnesium sulfate 0.9%, manganese sulfate 0.003%, surplus is water.
The technological condition for fermentation of the present embodiment is same as in Example 1.
Embodiment 5
A kind of enterococcus faecalis fermentation medium, it is made up of the component of following mass percent: sucrose 4%, peptone 1.6%,
Biological nitrogen source 2.5%, potassium dihydrogen phosphate 0.07%, dipotassium hydrogen phosphate 0.3%, magnesium sulfate 0.8%, manganese sulfate 0.004%, surplus is water.
The technological condition for fermentation of the present embodiment is same as in Example 1.
Embodiment 6
A kind of enterococcus faecalis fermentation medium, it is made up of the component of following mass percent: sucrose 5%, peptone 0.5%,
Biological nitrogen source 5%, potassium dihydrogen phosphate 0.01%, dipotassium hydrogen phosphate 1%, magnesium sulfate 0.1%, manganese sulfate 0.005%, surplus is water.
The technological condition for fermentation of the present embodiment is same as in Example 1.
Embodiment 7
A kind of enterococcus faecalis fermentation medium, it is made up of the component of following mass percent: sucrose 4.5%, peptone
1.2%, biological nitrogen source 4.5%, potassium dihydrogen phosphate 0.04%, dipotassium hydrogen phosphate 0.6%, magnesium sulfate 0.3%, manganese sulfate 0.004%, surplus
For water.
The technological condition for fermentation of the present embodiment is same as in Example 1.
Embodiment 8
A kind of enterococcus faecalis fermentation medium, it is made up of the component of following mass percent: sucrose 4%, peptone 0.8%,
Biological nitrogen source 3%, potassium dihydrogen phosphate 0.08%, dipotassium hydrogen phosphate 0.3%, magnesium sulfate 0.7%, manganese sulfate 0.003%, surplus is water.
The technological condition for fermentation of the present embodiment is same as in Example 1.
Embodiment 9
A kind of enterococcus faecalis fermentation medium, it is made up of the component of following mass percent: sucrose 2%, peptone 0.6%,
Biological nitrogen source 4%, potassium dihydrogen phosphate 0.06%, dipotassium hydrogen phosphate 0.4%, magnesium sulfate 0.1%, manganese sulfate 0.002%, surplus is water.
The technological condition for fermentation of the present embodiment is same as in Example 1.
Embodiment 10
A kind of enterococcus faecalis fermentation medium, it is made up of the component of following mass percent: sucrose 5%, peptone 1.5%,
Biological nitrogen source 2%, potassium dihydrogen phosphate 0.08%, dipotassium hydrogen phosphate 0.4%, magnesium sulfate 0.9%, manganese sulfate 0.001%, surplus is water.
The technological condition for fermentation of the present embodiment is same as in Example 1.
Embodiment 11
A kind of enterococcus faecalis fermentation medium, it is made up of the component of following mass percent: sucrose 3%, peptone 0.6%,
Biological nitrogen source 4%, potassium dihydrogen phosphate 0.08%, dipotassium hydrogen phosphate 0.2%, magnesium sulfate 0.2%, manganese sulfate 0.004%, surplus is water.
The technological condition for fermentation of the present embodiment is same as in Example 1.
Embodiment 12
A kind of enterococcus faecalis fermentation medium, it is made up of the component of following mass percent: sucrose 2%, peptone 2%, raw
Thing nitrogen source 4%, potassium dihydrogen phosphate 0.04%, dipotassium hydrogen phosphate 0.2%, magnesium sulfate 0.8%, manganese sulfate 0.003%, surplus is water.
The technological condition for fermentation of the present embodiment is same as in Example 1.
Embodiment 13
A kind of enterococcus faecalis fermentation medium, it is made up of the component of following mass percent: sucrose 3%, peptone 1.5%,
Biological nitrogen source 2%, potassium dihydrogen phosphate 0.03%, dipotassium hydrogen phosphate 0.6%, magnesium sulfate 0.7%, manganese sulfate 0.002%, surplus is water.
The technological condition for fermentation of the present embodiment is same as in Example 1.
Embodiment 14
A kind of enterococcus faecalis fermentation medium, it is made up of the component of following mass percent: sucrose 2%, peptone 0.5%,
Biological nitrogen source 4%, potassium dihydrogen phosphate 0.06%, dipotassium hydrogen phosphate 0.4%, magnesium sulfate 0.8%, manganese sulfate 0.003%, surplus is water.
The technological condition for fermentation of the present embodiment is same as in Example 1.
Embodiment 15
A kind of enterococcus faecalis fermentation medium, it is made up of the component of following mass percent: sucrose 5%, peptone 1.5%,
Biological nitrogen source 3%, potassium dihydrogen phosphate 0.09%, dipotassium hydrogen phosphate 0.6%, magnesium sulfate 0.3%, manganese sulfate 0.001%, surplus is water.
The technological condition for fermentation of the present embodiment is same as in Example 1.
Embodiment 16
A kind of enterococcus faecalis fermentation medium, it is made up of the component of following mass percent: sucrose 3.5%, peptone 2%,
Biological nitrogen source 2%, potassium dihydrogen phosphate 0.04%, dipotassium hydrogen phosphate 0.5%, magnesium sulfate 0.5%, manganese sulfate 0.002%, surplus is water.
The technological condition for fermentation of the present embodiment is same as in Example 1.
Embodiment 17
A kind of enterococcus faecalis fermentation medium, it is made up of the component of following mass percent: sucrose 2.5%, peptone 2%,
Biological nitrogen source 4.5%, potassium dihydrogen phosphate 0.07%, dipotassium hydrogen phosphate 0.8%, magnesium sulfate 0.3%, manganese sulfate 0.004%, surplus is water.
The technological condition for fermentation of the present embodiment is same as in Example 1.
Embodiment 18
A kind of enterococcus faecalis fermentation medium, it is made up of the component of following mass percent: sucrose 4%, peptone 1%, raw
Thing nitrogen source 1%, potassium dihydrogen phosphate 0.1%, dipotassium hydrogen phosphate 0.2%, magnesium sulfate 0.7%, manganese sulfate 0.003%, surplus is water.
The technological condition for fermentation of the present embodiment is same as in Example 1.
Embodiment 19
A kind of enterococcus faecalis fermentation medium, it is made up of the component of following mass percent: sucrose 5%, peptone 0.5%,
Biological nitrogen source 1%, potassium dihydrogen phosphate 0.1%, dipotassium hydrogen phosphate 1%, magnesium sulfate 0.1%, manganese sulfate 0.003%, surplus is water.
The technological condition for fermentation of the present embodiment is same as in Example 1.
The product that embodiment 2 ~ 19 cultivation obtains is for detecting, and testing result is as follows:
Claims (6)
1. an enterococcus faecalis fermentation medium, it is characterised in that it is made up of the component of following mass percent: sucrose 1%-
5%, peptone 0.5%-2%, biological nitrogen source 1%-5%, potassium dihydrogen phosphate 0.01%-0.1%, dipotassium hydrogen phosphate 0.1%-1%, magnesium sulfate
0.1%-1%, manganese sulfate 0.001%-0.005%, surplus is water.
Enterococcus faecalis fermentation medium the most according to claim 1, it is characterised in that it is by following mass percent
Component forms: sucrose 1%-3%, peptone 1.5%-2%, biological nitrogen source 1%-3%, potassium dihydrogen phosphate 0.01%-0.04%, phosphoric acid hydrogen two
Potassium 0.6%-1%, magnesium sulfate 0.4%-1%, manganese sulfate 0.004%-0.005%, surplus is water.
Enterococcus faecalis fermentation medium the most according to claim 1, it is characterised in that it is by following mass percent
Component forms: sucrose 3.1%-5%, peptone 0.5%-1.4%, biological nitrogen source 3.1%-5%, potassium dihydrogen phosphate 0.05%-0.1%, phosphorus
Acid hydrogen dipotassium 0.1%-0.55%, magnesium sulfate 0.1%-0.35%, manganese sulfate 0.001%-0.003%, surplus is water.
Enterococcus faecalis fermentation medium the most according to claim 1, it is characterised in that it is by following mass percent
Component forms: sucrose 3%, peptone 1%, biological nitrogen source 2%, potassium dihydrogen phosphate 0.05%, dipotassium hydrogen phosphate 0.5%, magnesium sulfate
0.5%, manganese sulfate 0.002%, surplus is water.
Enterococcus faecalis fermentation medium the most according to claim 1, it is characterised in that: described biological nitrogen source is mainly by amino
Acid, vitamin and mineral composition.
Enterococcus faecalis fermentation medium the most according to claim 1, it is characterised in that: dry in the composition in described biological nitrogen source
Material is more than 70%, and total nitrogen is more than 8%, and amino-acid nitrogen is more than 2%, and ash is less than 15%, pH value 5.0-6.5.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201610760483.4A CN106190926A (en) | 2016-08-30 | 2016-08-30 | A kind of enterococcus faecalis fermentation medium |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201610760483.4A CN106190926A (en) | 2016-08-30 | 2016-08-30 | A kind of enterococcus faecalis fermentation medium |
Publications (1)
Publication Number | Publication Date |
---|---|
CN106190926A true CN106190926A (en) | 2016-12-07 |
Family
ID=58089677
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201610760483.4A Pending CN106190926A (en) | 2016-08-30 | 2016-08-30 | A kind of enterococcus faecalis fermentation medium |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN106190926A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN115745674A (en) * | 2022-11-04 | 2023-03-07 | 江西农业大学 | Microbial oligosaccharide chelated trace element water-soluble fertilizer and preparation method thereof |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103820363A (en) * | 2014-01-27 | 2014-05-28 | 福建省农业科学院生物技术研究所 | Preparation and application of enterococcus faecium powder |
CN103981116A (en) * | 2013-12-24 | 2014-08-13 | 北京伟嘉人生物技术有限公司 | Culture method and application of enterococcus faecium |
CN104560820A (en) * | 2014-12-30 | 2015-04-29 | 杭州师范大学 | Enterococcus faecium KQ2.6 and application thereof |
-
2016
- 2016-08-30 CN CN201610760483.4A patent/CN106190926A/en active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103981116A (en) * | 2013-12-24 | 2014-08-13 | 北京伟嘉人生物技术有限公司 | Culture method and application of enterococcus faecium |
CN103820363A (en) * | 2014-01-27 | 2014-05-28 | 福建省农业科学院生物技术研究所 | Preparation and application of enterococcus faecium powder |
CN104560820A (en) * | 2014-12-30 | 2015-04-29 | 杭州师范大学 | Enterococcus faecium KQ2.6 and application thereof |
Non-Patent Citations (2)
Title |
---|
徐州市为天科技有限公司: "生物氮源", 《网页证据》 * |
李振华等: "屎肠球菌扩大发酵的培养基优化", 《CHINA BREWING》 * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN115745674A (en) * | 2022-11-04 | 2023-03-07 | 江西农业大学 | Microbial oligosaccharide chelated trace element water-soluble fertilizer and preparation method thereof |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Hayek et al. | Cultivation media for lactic acid bacteria used in dairy products | |
US20210395677A1 (en) | Microorganism-Derived Protein Hydrolysates and Methods of Preparation and Use Thereof | |
JP2024028821A (en) | Microbial conversion of co2 and other c1 substrates to vegan nutrients, fertilizers, biostimulants, and systems for accelerated soil carbon sequestration | |
KR101604633B1 (en) | Medium composition for culturing lactic acid bacteria and producing method of powder of lactic acid bacteria using the same | |
CN104928208B (en) | Lactobacillus plantarum Lp90, and screening method and application thereof | |
CN103504123A (en) | Fermented soybean meal with function of complex enzymes and preparation method for fermented soybean meal | |
Tian et al. | Exploring cellular fatty acid composition and intracellular metabolites of osmotic-tolerant mutant Lactobacillus paracasei NCBIO-M2 for highly efficient lactic acid production with high initial glucose concentration | |
CN103951486A (en) | Plant nutrition regulation liquid fertilizer and its production method | |
CN104164459A (en) | Method utilizing fermentation to improve gamma-aminobutyric acid content of brown rice | |
Nunes et al. | Enhanced production of single cell protein from M. capsulatus (Bath) growing in mixed culture | |
CN103509832B (en) | Method for performing fermentation production on gamma-aminobutyric acid by using high-concentration monopotassium phosphate as buffer salt | |
CN103992165B (en) | A kind of complex micro organism fungicide | |
CN106399155A (en) | Bacillus licheniformis fermentation culture medium | |
KR20230044134A (en) | New silage additive composition | |
Lee et al. | A low-cost Lactobacillus salivarius L29 growth medium containing molasses and corn steep liquor allows the attainment of high levels of cell mass and lactic acid production | |
CN106190926A (en) | A kind of enterococcus faecalis fermentation medium | |
CN106148245A (en) | A kind of fermentation of bacillus subtilis culture medium | |
Song et al. | Optimal production of exopolysaccharide by Bacillus licheniformis KS-17 isolated from kimchi | |
CN110257306A (en) | One lactobacillus plantarum and its application | |
KR101236309B1 (en) | Medium composition for high concentration culture of Bacillus and uses thereof | |
CN105994940B (en) | Bioactive protein feed and preparation method thereof | |
US9809795B2 (en) | Extraction of nitrogen from organic materials through ammonification by mixed bacterial populations | |
US20080026441A1 (en) | Production of probiotic bacteria using maple sap | |
RU2658977C1 (en) | Method for producing protein fodder additive | |
Paliy et al. | Enhanced cultivation technology for lacto and bifidobacteria |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
RJ01 | Rejection of invention patent application after publication |
Application publication date: 20161207 |
|
RJ01 | Rejection of invention patent application after publication |