Method for efficiently identifying/screening clostridium butyricum and application thereof

A technology for identifying Clostridium and Ding, which is applied in the field of microorganisms, can solve the problems of difficult screening, low ratio, and difficulty in obtaining, etc., and achieve the effects of improving screening efficiency, speeding up the experiment process, and long screening cycle

Active Publication Date: 2019-12-20
JIANGNAN UNIV
View PDF3 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the specificity of the RCM agar medium is poor, and Clostridium butyricum is not the dominant strain in the intestinal tract and soil, and its relative abundance is low, which makes the final screening more difficult
The specificity of TSN agar medium is higher than that of RCM agar medium, but due to the uneven distribution of Clostridium butyricum in samples, especi...

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
  • Method for efficiently identifying/screening clostridium butyricum and application thereof
  • Method for efficiently identifying/screening clostridium butyricum and application thereof
  • Method for efficiently identifying/screening clostridium butyricum and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0042] Embodiment 1 identifies the method for Clostridium butyricum

[0043] Design the following primers:

[0044] (1) The sequences of primers CBU21F / CBU1023R are:

[0045] Forward primer: 5'-TCAATTAGAAGGCAGAGTACC-3' (SEQ ID NO: 1)

[0046] Reverse primer: 5'-CTAAAACTGACTGTGGCATT-3' (SEQ ID NO: 2)

[0047] The size of the amplified target gene fragment is 1022bp;

[0048] (2) The sequences of primers CBU80F / CBU551R are:

[0049] Forward primer: 5'-CAAAGTCATCATCTAGTCGT-3' (SEQ ID NO: 3)

[0050] Reverse primer: 5'-TCCATTATAAGCTGGTGCAT-3' (SEQ ID NO: 4)

[0051] The size of the amplified target gene fragment is 491bp;

[0052] (3) The sequences of primers CBU64F / CBU488R are:

[0053] Forward primer: 5'-TACACTCCTATCATCACCCTTTAT-3' (SEQ ID NO:5)

[0054] Reverse primer: 5'-CACCTAAATCGGCAGCAGCAT-3'SEQ ID NO:6

[0055] The size of the amplified target gene fragment is 445bp.

[0056] Template DNA extraction: Genomic DNA was extracted from 20 Clostridium butyricum and 12 ...

Embodiment 2

[0062] Embodiment 2 screens the method for Clostridium butyricum

[0063] Based on the TSN selective medium, the screening of Clostridium butyricum in the fecal samples with the target band amplified was completed. Dilute the samples in a gradient manner, spread 100 μL of each dilution on the TSN selective medium plate, culture anaerobically at 37°C for 48 hours, select a single colony that grows normally under anaerobic conditions, and streak on the TSN selective medium plate After isolation and incubation at 37°C for 48 hours, a single colony similar in colony morphology to Clostridium butyricum was selected. Carry out PCR amplification according to the method of Example 1, and obtain the corresponding specific target band as the target strain.

Embodiment 3

[0064] Example 3 High-efficiency identification / screening of the accuracy detection of Clostridium butyricum PCR amplification primers

[0065] CBU21F / CBU1023R, CBU80F / CBU551R and CBU64F / CBU488R were used as primers to detect the accuracy of PCR amplification primers.

[0066] Extract the genomic DNA of 20 strains of Clostridium butyricum from different samples, use the optimized primers CBU21F / CBU1023R and the reaction system and reaction program in Example 1 to carry out PCR amplification, and detect the specificity of the PCR amplification primers of the present invention. sex. The results of agarose gel electrophoresis figure 1 shown, from figure 1 It can be seen that the specific primer CBU21F / CBU1023R used to amplify Clostridium butyricum in this embodiment can accurately amplify the target sequence fragments of 20 strains of Clostridium butyricum, which is a positive result, and the water control reaction No amplification band was detected, which was a negative resul...

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 method for efficiently identifying/screening clostridium butyricum and application thereof, and belongs to the technical field of microorganisms. Specific primers are designed according to the core gene of the clostridium butyricum, and the specific primers are used for screening and identifying the clostridium butyricum. Compared with traditional screening methods basedon a TSN selective medium, the PCR method for efficiently screening clostridium butyricum provided by the invention is high in accuracy up tp 100%, high in specificity and high in sensitivity, and thedetection limit is 7.95x10<-3> ng/[mu]L. The method can reduce the range of screened samples, improve the probability of screening out target strains, effectively shorten the screening period, reducethe workload and improve the screening efficiency.

Description

technical field [0001] The invention relates to a method for efficiently identifying / screening Clostridium butyricum and its application, belonging to the technical field of microorganisms. Background technique [0002] Clostridium butyricum, also known as Clostridium butyricum, is a Gram-positive anaerobic bacterium belonging to the Bacillus family and the genus Clostridium. Widely present in cheese, natural yogurt, human and animal manure and soil. Clostridium butyricum produces gas during the fermentation process, and the fermentation products include acetic acid, butyric acid, butanol, amylase, lipase, vitamins, etc. The study of Clostridium butyricum as a microecological agent was first discovered and reported by a Ph.D. from Chiba Medical College in Japan in 1933. Since then, Clostridium butyricum has been widely used as a enteritis treatment drug, food additive, veterinary drug and feed additive because it can regulate the microecological balance of the human intest...

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
IPC IPC(8): C12Q1/689C12Q1/04C12R1/145
CPCC12Q1/689
Inventor 陈卫陆文伟易至翟齐啸崔树茂赵建新张灏
Owner JIANGNAN UNIV
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products

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

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap