CN102719386B - Bacterium and fungus strain storage culture medium - Google Patents

Bacterium and fungus strain storage culture medium Download PDF

Info

Publication number
CN102719386B
CN102719386B CN 201210242292 CN201210242292A CN102719386B CN 102719386 B CN102719386 B CN 102719386B CN 201210242292 CN201210242292 CN 201210242292 CN 201210242292 A CN201210242292 A CN 201210242292A CN 102719386 B CN102719386 B CN 102719386B
Authority
CN
China
Prior art keywords
bacterium
culture medium
agar
glycerine
strain storage
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.)
Expired - Fee Related
Application number
CN 201210242292
Other languages
Chinese (zh)
Other versions
CN102719386A (en
Inventor
苏桂华
崔海玲
王金环
王海鹏
Original Assignee
苏桂华
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 苏桂华 filed Critical 苏桂华
Priority to CN 201210242292 priority Critical patent/CN102719386B/en
Publication of CN102719386A publication Critical patent/CN102719386A/en
Application granted granted Critical
Publication of CN102719386B publication Critical patent/CN102719386B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Micro-Organisms Or Cultivation Processes Thereof (AREA)

Abstract

The invention relates to a bacterium and fungus strain storage culture medium comprising the following components: tryptone, sodium chloride, agar, yeas extract and glycerol. The tryptone is used for providing a microorganism nitrogen source; the sodium chloride is used for maintaining a uniform osmotic pressure; the agar is used as a supporting component in the culture medium; the yeas extract is rich in proteins, amino acids, peptides, nucleotides and vitamins B and can be used for replenishing various vitamins, amino acids and growth factors for the growth of microorganisms; and the glycerol is used as a carbon source and can be used for playing roles of preventing freeze and preserving moisture. The bacterium and fungus strain storage culture medium is simple and convenient in operation of strain storage, long in storage time, high in stability and capable of increasing the survival rate and the reproductive rate of the strains.

Description

A kind of bacterium, fungi strain are preserved substratum
Technical field
The present invention relates to preserve the technical field of bacterial classification, specifically a kind of bacterium, fungi strain are preserved substratum.
Background technology
At present bacterial classification store method commonly used has freeze-drying, semisolid medium method and simple glycerine preservation method etc.These methods have certain defective, and as freeze-drying, the preparation process complexity needs appointed condition preferably again; The semisolid medium preservation method can not be preserved bacterial classification for a long time; Simple its glycerine of glycerine preservation method is just preserved moisture for antifreeze, and some special bacterial strain survival rate in glycerine stoste is low, and the shelf time is short, and toxicity descends.
Summary of the invention
The present invention is directed to the prior art deficiency, provide a kind of preservation bacterial classification easy and simple to handle, the shelf time is long, and the bacterium of good stability, fungi strain are preserved substratum.
Technical scheme of the present invention is: a kind of bacterium, fungi strain preserve substratum, it is characterized in that it is made up of the following raw materials in weight proportioning: Tryptones 0.8-1.2g, sodium-chlor 0.8-1.2g, agar 0.2-0.5g, yeast extract paste 0.3-0.6g, glycerine 15ml, distilled water 85ml.
Preparation method's step is as follows: A, add Tryptones, sodium-chlor, agar, yeast extract paste, glycerine in the distilled water in proportion; B, heating for dissolving are transferred PH7.5; C, be divided in the EP pipe every pipe 0.5-1ml, D, 8 pounds of sterilizations in 20 minutes ,-20 ℃ of preservations.
Tryptones among the present invention provides the microorganism nitrogenous source; Sodium-chlor is kept balanced osmotic pressure; Agar is the support composition in the substratum; Yeast extract paste rich in proteins, amino acid, peptide class, Nucleotide, vitamin B group can replenish nitrogenous source and various VITAMIN, amino acid and somatomedin that microorganism growth is provided; Glycerine has antifreeze and moisture-keeping function as carbon source.
The present invention has the following advantages: preparation is simple, easily, and cost is low, and is easy to use, and it is easy and simple to handle to preserve bacterial classification, and the shelf time is long, and good stability improves survival rate and the breeding potential of bacterial classification greatly.
Embodiment
Embodiment 1: a kind of bacterium, fungi strain are preserved substratum, prepare according to following column data and described step: Tryptones 0.8-1.2g, sodium-chlor 0.8-1.2g, agar 0.2-0.5g, yeast extract paste 0.3-0.6g, glycerine 15ml, distilled water 85ml.
Preparation method's step is as follows: A, add Tryptones, sodium-chlor, agar, yeast extract paste, glycerine in the distilled water in proportion; B, heating for dissolving are transferred PH7.5; C, be divided in the EP pipe every pipe 0.5-1ml, D, 8 pounds of sterilizations in 20 minutes ,-20 ℃ of preservations.
Embodiment 2: a kind of bacterium, fungi strain are preserved substratum, prepare according to following column data and described step: Tryptones 1.0g, sodium-chlor 1.0g, agar 0.3g, yeast extract paste 0.5g, glycerine 15ml, distilled water 85ml.
Preparation method's step is as follows: A, remove Tryptones 1.0g, and sodium-chlor 1.0g, agar 0.3g, yeast extract paste 0.5g, glycerine 15ml add in the distilled water; B, heating for dissolving are transferred PH7.5; C, be divided in the EP pipe every pipe 0.5-1ml, D, 8 pounds of sterilizations in 20 minutes ,-20 ℃ of preservations.
Embodiment 3: a kind of bacterium, fungi strain are preserved substratum, prepare according to following column data and described step: Tryptones 0.9g, sodium-chlor 0.9g, agar 0.4g, yeast extract paste 0.6g, glycerine 15ml, distilled water 85ml.
Preparation method's step is as follows: A, get Tryptones 0.9g, and sodium-chlor 0.9g, agar 0.4g, yeast extract paste 0.6g, glycerine 15ml add in the distilled water; B, heating for dissolving are transferred PH7.5; C, be divided in the EP pipe every pipe 0.5-1ml, D, 8 pounds of sterilizations in 20 minutes ,-20 ℃ of preservations.
Embodiment 4: a kind of bacterium, fungi strain are preserved substratum, prepare according to following column data and described step: Tryptones 1.2g, sodium-chlor 1.2g, agar 0.5g, yeast extract paste 0.4g, glycerine 15ml, distilled water 85ml.
Preparation method's step is as follows: A, get Tryptones 1.2g, and sodium-chlor 1.2g, agar 0.5g, yeast extract paste 0.4g, glycerine 15ml add in the distilled water; B, heating for dissolving are transferred PH7.5; C, be divided in the EP pipe every pipe 0.5-1ml, D, 8 pounds of sterilizations in 20 minutes ,-20 ℃ of preservations.
Effect is judged:
Bacterial classification to be preserved scraped with transfering loop get 4-5 ring, place the EP pipe that above-mentioned substratum is housed ,-20 ℃ of refrigerators are preserved.The bacterial classification of preserving has bacterial classifications such as streptococcus aureus, escherichia coli, Pseudomonas aeruginosa, Salmonella typhi and Candida albicans, show through the saving result more than 5 years, the morphological structure of bacterium, dyeing property, biochemical reaction, antigenic structure etc. all conforms to reference culture.

Claims (2)

1. a bacterium, fungi strain are preserved substratum, it is characterized in that it is made up of the following raw materials in weight proportioning: Tryptones 0.8-1.2g, sodium-chlor 0.8-1.2g, agar 0.2-0.5g, yeast extract paste 0.3-0.6g, glycerine 15ml, distilled water 85ml.
2. bacterium as claimed in claim 1, fungi strain preserve the preparation method of substratum, it is characterized in that step is as follows: A, add Tryptones, sodium-chlor, yeast extract paste, agar, glycerine in the distilled water in proportion; PH7.5 is transferred in B, heating fusion; C, be divided in the EP pipe every pipe 0.5-1ml, D, 8 pounds of sterilizations in 20 minutes ,-20 ℃ of preservations.
CN 201210242292 2012-07-01 2012-07-01 Bacterium and fungus strain storage culture medium Expired - Fee Related CN102719386B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN 201210242292 CN102719386B (en) 2012-07-01 2012-07-01 Bacterium and fungus strain storage culture medium

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN 201210242292 CN102719386B (en) 2012-07-01 2012-07-01 Bacterium and fungus strain storage culture medium

Publications (2)

Publication Number Publication Date
CN102719386A CN102719386A (en) 2012-10-10
CN102719386B true CN102719386B (en) 2013-08-28

Family

ID=46945259

Family Applications (1)

Application Number Title Priority Date Filing Date
CN 201210242292 Expired - Fee Related CN102719386B (en) 2012-07-01 2012-07-01 Bacterium and fungus strain storage culture medium

Country Status (1)

Country Link
CN (1) CN102719386B (en)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103642886A (en) * 2013-11-18 2014-03-19 宁夏泰瑞制药股份有限公司 Medium for producing demethylchlortetracycline by fermenting streptomyces aureus and culturing method
CN103718830B (en) * 2013-12-27 2015-08-19 湖南农业大学 A kind of factorial praluction pleurotus eryngii quel strains cryopreservation method
CN104498380A (en) * 2014-08-04 2015-04-08 湖北文理学院 Staphylococcus ATCC25923 proliferation promoter and application method thereof
CN105602849A (en) * 2014-09-05 2016-05-25 杭州致远医学检验所有限公司 Special sample tissue storage and transportation culture medium for Helicobacter pylori separation culture
CN104673685B (en) * 2015-03-16 2018-11-16 广西中医药大学 A kind of isolation medium of Radix zanthoxyli endogenetic fungus
CN108949572A (en) * 2018-08-21 2018-12-07 卓源健康科技有限公司 A kind of caprophyl freezen protective liquid and its store method
CN112159786B (en) * 2020-11-04 2022-03-01 河北科技大学 Cr (VI) reducing strain C6, and culture condition and application thereof

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1096819A (en) * 1993-06-23 1994-12-28 铜陵市卫生防疫站 A kind of long-acting preservative jejunum campylobacter colony culture medium and preparation method
CN102465097A (en) * 2010-11-10 2012-05-23 中国科学院生态环境研究中心 Method for long-term preservation and rapid recovery of luminous bacterium strain
CN102174435A (en) * 2011-01-21 2011-09-07 贵州大学 Bacillus subtilis strain and application thereof
CN102433373B (en) * 2011-12-14 2013-10-09 浙江省农业科学院 Salmonella characteristic chromogenic liquid nutrient medium, preparation method thereof and rapid detection method of salmonella

Also Published As

Publication number Publication date
CN102719386A (en) 2012-10-10

Similar Documents

Publication Publication Date Title
CN102719386B (en) Bacterium and fungus strain storage culture medium
Sui et al. Responses of yeast biocontrol agents to environmental stress
Adamec Respiration and photosynthesis of bladders and leaves of aquatic Utricularia species
EP3642323B1 (en) Method for preserving a sample of bacteria
Manzanera et al. High survival and stability rates of Escherichia coli dried in hydroxyectoine
CN102524518B (en) Method for producing antibacterial peptide by using brevibacillus laterosporu
CN102311919B (en) Microalgae species preserving method
Turk et al. Glycerol metabolism genes in Aureobasidium pullulans and Aureobasidium subglaciale
Li et al. The potential productivity of the microalga, Nannochloropsis oceanica SCS-1981, in a solar powered outdoor open pond as an aquaculture feed
JP2017123816A (en) Foods, heat treatment method of foods, manufacturing method of phycocyanin, manufacturing method of organic acid and manufacturing method of hydrogen
CN102643749B (en) Microorganism low-temperature preservation protective agent and microorganism low-temperature preservation method
Navarta et al. Postharvest control of gray mold in apples with lyophilized formulations of Cryptococcus laurentii: the effect of cold stress in the survival and effectiveness of the yeast
Di Martino et al. Effect of exogenous proline on the ethanolic tolerance and malolactic performance of Oenococcus oeni
CN101606552B (en) Bifidobacterium deep freezing direct vat starter culture and composite cryoprotectant thereof
CN102994388B (en) Strain preservation liquid and strain preservation method
CN110804553B (en) Culture medium for improving preservation survival rate of lactic acid bacteria and application thereof
Indah et al. Preliminary studies of halophilic yeasts antimicrobial activities isolated from cocoa bean pulp towards E. coli and Salmonella spp
Babich et al. Structure and properties of antimicrobial peptides produced by antagonist microorganisms isolated from Siberian natural objects.
JP2008530995A (en) Method for modifying the viability of freeze-dried microorganisms by gassing growth medium
CN1358838A (en) Preservation method for live bacterial preparation
Marco et al. Influence of addition of yeast autolysate on the formation of amines in wine
de Arruda Moura Pietrowski et al. Viability of Hanseniaspora uvarum yeast preserved by lyophilization and cryopreservation
JP2017512477A5 (en)
Liu et al. iTRAQ‐based quantitative proteomic analysis of the effect of heat shock on freeze‐drying of Lactobacillus acidophilus ATCC4356
Savkina et al. Cryopreservation to be a progressive method for keeping up valuable strains of lactic acid bacteria and yeasts.

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20130828

Termination date: 20140701

EXPY Termination of patent right or utility model