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

2017-m2 strain containing mannanase gene

A 2017-M2, mannanase technology, which is applied in glycosylase, genetic engineering, plant genetic improvement, etc., can solve the problem that the type and quantity of mannanase strains cannot meet the needs of natural red pigment producing bacteria resources and other problems to achieve the effect of low requirements for culture conditions and fast growth

Active Publication Date: 2022-06-10
武汉设计工程学院
View PDF1 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0007] The object of the present invention is to overcome the defective of prior art, and the kind and quantity of existing mannanase bacterial classification can not satisfy industry to the demand of natural red pigment producing bacterium resource

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
  • 2017-m2 strain containing mannanase gene
  • 2017-m2 strain containing mannanase gene
  • 2017-m2 strain containing mannanase gene

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0041] Example 1 Isolation, screening and identification of Talaromyces atroroseus 2017-M2 strain

[0042] 1. Isolation of Talaromyces atroroseus 2017-M2 strain

[0043] (1) Talaromyces atroroseus 2017-M2 strain was isolated from the soil 5 cm below the ground in Tangxun Lake area, Jiangxia District, Wuhan City, Hubei Province, where Wuhan Institute of Design and Engineering, Wuhan City, Hubei Province is located. The specific steps are: take 10 g of soil, dilute it 10 times with 90 mL of sterile water, shake well, clarify, and then continue to dilute to 1,000 times; take 0.1 mL of the 1,000-fold dilution and spread it on a Martin Bengal red solid plate, cultivate for 3 days, The culture was continued at room temperature until the 7th day, and the growth of the colonies in the petri dish and the production of water-soluble red pigment in the medium were observed. Pick Penicillium-like colonies that produce red pigment. Pure cultures were streaked in Gaw's No. 1 solid plates....

Embodiment 2

[0053] Example 2 Application of Talaromyces atroroseus2017-M2 strain fermentation production and extraction of red pigment

[0054] In this example, the Talaromyces atroroseus 2017-M2 strain was inoculated into a fermentation medium (a 500mL conical flask was filled with 100mL fermentation medium), and the fermentation medium was a PDA liquid medium: peeled potatoes 200g to 30min, take 1000mL of potato juice, add Glucose 20g, packaged and sterilized, pH 7.0, cultured at 30°C, 200rpm shaker for 5d-7d. Bacterial liquid was centrifuged at 8000rpm and 10min to obtain fermentation broth, and sterilized by bacterial filter filtration, and the obtained filtrate was the crude extract of red pigment. The crude extract of red pigment was placed in a rotary evaporator at 70°C for vacuum concentration until it became a paste, and the obtained product was the crude extract of red pigment.

[0055] The obtained red pigment crude extract was dissolved in the same amount of distilled water a...

Embodiment 3

[0059] Example 3 Identification of cellulase produced by Talaromyces atroroseus 2017-M2 strain

[0060] Pick the strains and spot them on the cellulose identification medium with a toothpick, incubate at 28°C for 5-7 days, cover the medium with 1 mg / ml Congo red solution for 15 minutes, pour out the Congo red solution, and wash with 1 mol / L NaCl solution The Congo red solution was removed for 15 minutes, the NaCl solution was poured out, and a transparent circle was observed, indicating that the Talaromyces atroroseus 2017-M2 strain had the ability to produce cellulase.

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 belongs to the field of agricultural microorganism application, and relates to a 2017-M2 strain containing a mannanase gene. The strain can produce edible red pigment, mannanase and cellulase. isolated from the soil. It is Talaromyces atroroseus of the genus Talaromyces atroroseus, wherein the mannanase gene sequence is shown in SEQ ID NO:2. The similarity with the known mannan β-1,4-endonuclease gene is only 71%, which is a new functional gene and has wide application value. The strain grows well at 22°C-35°C, produces cellulase, mannanase and amylase, does not produce protease, and has no antibacterial effect. The red pigment with the maximum absorbance value at 600nm can be obtained in PDA medium. The active gene can be expressed in Escherichia coli. The optimal induction condition is 1.5μL of 1mM IPTG, induced for 3h at 37°C.

Description

technical field [0001] The invention belongs to the technical field of agricultural microorganism application, and in particular relates to a Talaromyces atroroseus 2017-M2 strain containing a mannanase gene and capable of producing edible red pigment, cellulase and mannanase. Isolated from soil, it is Talaromyces.atroroseus, which is evolved from Penicillium branch, belongs to a new strain, contains mannanase gene, the mannan expressed by this gene The enzyme is β-1,4-endomannanase. Background technique [0002] Talaromyce atroroseus is a new species of fungus discovered in 2013, which is classified as Talaromyces.atroroseus. The fungus is present in soil and fruit and was originally identified from house dust collected in South Africa. It produces large amounts of red pigment and does not contain any known mycotoxins. The genome of the strain contains a gene encoding β-1,4-mannanase, and β-mannanase (endo-1,4-β-mannanase) is an endohydrolase, which can act on the mannos...

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): C12N1/14C12N15/56C12N9/42C12P1/02C12R1/645
CPCC12N9/2491C12Y302/01025C12N9/2437C12Y302/01004C12P1/02C12R2001/645C12N1/145
Inventor 石慧翟淑红张娟莫晨阳欧炜明
Owner 武汉设计工程学院
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