Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Legionnella selective separation medium

A separation medium and selective technology, applied in the field of medium, can solve the problems of unfavorable popularization and application, high detection cost, high price, etc., and achieve the effects of easy popularization and application, increase positive rate and reduce detection cost

Active Publication Date: 2011-08-03
贵州金域医学检验中心有限公司
View PDF0 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0002] At present, the legionella isolation medium recognized at home and abroad are BCYEα-CCVC, BCYEα-GVPC and BCYEα-GPVA produced by bioMérieux in France, OXOID in the United Kingdom, BD in the United States, DIFCO, etc. [1] Most of these mediums are expensive (18-25 yuan / plate), and when they are widely used in hospital clinics and health and epidemic prevention departments, the detection cost is high, and the positive rate of Legionella isolation and culture is generally 35.1%-65.0% [2-3] , the positive rate is relatively low
Therefore existing legionella isolation culture medium is unfavorable for clinical and sanitation and epidemic prevention department popularization and application

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Legionnella selective separation medium
  • Legionnella selective separation medium
  • Legionnella selective separation medium

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0030] Legionella selective isolation culture medium, the component parts by weight that it comprises are as follows:

[0031] Base fluid:

[0032]

[0033] protein solution:

[0034] Glycine 2.8~3.2

[0035] L-cysteine ​​0.4~0.6

[0036] Albumin 0.08~0.12

[0037] Dye solution:

[0038] Bromocresol purple 0.008~0.012

[0039] Bromophenol blue 0.008~0.012

[0040] Antibiotic solution:

[0041] Vancomycin 0.0008~0.0012

[0042] Polymyxin B 0.0070.009

[0043] Cycloheximide 0.007~0.009

[0044] The preparation steps are as follows:

[0045] (1) Yeast powder, agar, carbon powder, ACES and a-ketoglutaric acid in the base liquid are weighed according to the above parts by weight and placed in a container, add 930-980 parts of water, and adjust the pH value to 6.85 with KOH; boil 1 minute, then high temperature sterilization at 121°C for 15 minutes; dissolving ferric pyrophosphate in 9 to 11 parts of water, filter sterilization; yeast powder, agar, carbon powder, ACES ...

Embodiment 2

[0051] Legionella selective isolation culture medium (BCYEα+DGVPC), the component parts by weight that comprise are as follows:

[0052] Base fluid:

[0053]

[0054] protein solution:

[0055] Glycine 3.0

[0056] L-cysteine ​​0.5

[0057] Albumin 0.1

[0058] Dye solution:

[0059] Bromocresol Violet 0.01

[0060] Bromophenol blue 0.01

[0061] Antibiotic solution:

[0062] Vancomycin 0.001

[0063] Polymyxin B 0.008

[0064] Cycloheximide 0.008

[0065] The preparation steps are as follows:

[0066] (1) Yeast powder, agar, carbon powder, ACES and α-ketoglutaric acid in the base liquid are weighed and placed in a container according to the above parts by weight, add 950 parts of water, and adjust the pH value to 6.85 with KOH; boil 1 minute, then autoclave (15 lbs) at 121°C for 15 minutes; dissolve ferric pyrophosphate in 10 parts water and filter sterilize; autoclave yeast powder, agar, carbon powder, ACES and a-ketone Glutaric acid, after cooling to 55°C, ad...

Embodiment 3

[0072] Legionella selective isolation culture medium, the component parts by weight that it comprises are as follows:

[0073] Base fluid:

[0074]

[0075]

[0076] protein solution:

[0077] Glycine 2.5

[0078] L-cysteine ​​0.3

[0079] Albumin 0.05

[0080] Dye solution:

[0081] Bromocresol Violet 0.005

[0082] Bromophenol blue 0.005

[0083] Antibiotic solution:

[0084] Vancomycin 0.0005

[0085] Polymyxin B 0.006

[0086] Cycloheximide 0.006

[0087] The preparation steps are as follows:

[0088] (1) Yeast powder, agar, carbon powder, ACES and a-ketoglutaric acid in the base liquid are weighed according to the above parts by weight and placed in a container, add 900 parts of water, adjust the pH value to 6.85 with KOH; boil for 1 minute , and then sterilized at 121°C for 15 minutes; dissolved ferric pyrophosphate in 8 parts of water, and sterilized by filtration; cooled yeast powder, agar, carbon powder, ACES and a-ketoglutaric acid after high temperatu...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention discloses a legionnella selective separation medium. Dyes such as bromothymol blue and bromocresol purple are added to the basic formulation of the basic medium of legionnella BCYE alpha and legionnella selective antibiotics of glycin, vancocin, polymyxin B and actinone are also added. The added dyes produce pigment in the growth process of legionnella; the shape and the color of a colony are beneficial to identifying and distinguishing a target bacterium of the legionnella; the concentrations of the selective antibiotics are added and regulated, the inhibiting capability to non-legionnella and microbial class is enhanced and the inhibiting performance for the legionnella is reduced, thereby enhancing the positive rate for the separation culture of the legionnella; the detection cost is reduced and the legionnella selective separation medium is economic and practical and is convenient for popularization and application for clinical and health and epidemic prevention departments.

Description

technical field [0001] The invention relates to a culture medium, in particular to a selective separation culture medium for Legionella which is suitable for the isolation and cultivation of Legionella in environmental and clinical specimens, can reduce the pollution of miscellaneous bacteria, and improve the positive rate of Legionella isolation and culture. Background technique [0002] At present, the legionella isolation medium recognized at home and abroad are BCYEα-CCVC, BCYEα-GVPC and BCYEα-GPVA produced by bioMérieux in France, OXOID in the United Kingdom, BD in the United States, DIFCO, etc. [1] Most of these mediums are expensive (18-25 yuan / plate), and when they are widely used in hospital clinics and health and epidemic prevention departments, the detection cost is high, and the positive rate of Legionella isolation and culture is generally 35.1%-65.0% [2-3] , the positive rate is relatively low. Therefore existing legionella isolation culture medium is unfavora...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Patents(China)
IPC IPC(8): C12N1/20C12Q1/04C12R1/01
Inventor 朱庆义胡朝晖詹晓勇王娟张远志
Owner 贵州金域医学检验中心有限公司
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com