Medium-temperature beta-glucosidase BglA1, gene of same and application of same

A technology of glucosidase, ppic9-bgla1, applied in the field of genetic engineering, can solve problems such as poor thermal stability and inability to meet medium and high temperature industrial processing

Active Publication Date: 2012-02-22
WUHAN SUNHY BIOLOGICAL
View PDF5 Cites 14 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] At present, the glucosidase derived from Trichoderma is used in industry, but its thermal stability is poor, and it cannot meet the long-term medium and high temperature industrial treatment. Therefore, a new type of β-glucosidase with good heat resistance is obtained. has great significance

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
  • Medium-temperature beta-glucosidase BglA1, gene of same and application of same
  • Medium-temperature beta-glucosidase BglA1, gene of same and application of same
  • Medium-temperature beta-glucosidase BglA1, gene of same and application of same

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0082] Example 1 Separation of Phialophora sp.XH6 and Enzyme Production Characteristics

[0083] Phialophora sp.XH6 is isolated from tin ore waste liquid in Yunnan mining area, pH3.0. The isolation medium is PDA medium, pH 3.0, and single bacteria are obtained by multiple dilution and plating. In the PDA medium for 14 days at 28°C, the colonies are flat, compact, dark brown, and 1.5-2 cm in diameter. Mycelium superficial or buried, mycelia light brown, smooth, septate, branched and form a network. The conidiophores are short, some are bottle-shaped, dark, and the conidiophores are solitary or verticillate. Conidia translucent to dark. Unicellular. Spherical to oval. The bacterium belongs to the genus Phialophora and is named XH6 (Phialophora sp.). The strain was preserved on October 21, 2011 in the General Microbiology Center of the China Committee for the Collection of Microbial Cultures (No. 3, No. 1, Beichen West Road, Chaoyang District, Beijing, Institute of Microbio...

Embodiment 2

[0085] Example 2 Cloning of Phialophora XH6 (Phialophora sp.) β-glucosidase Encoding Gene BglA1

[0086] Extraction of Phialaphora XH6 (Phialophora sp.) Genomic DNA:

[0087] Centrifuge the culture of PDB liquid cultured at 30°C for 5 days to collect the bacteria, put it in a mortar and grind it with liquid nitrogen for 5 minutes, add 10mL of CTAB extract, put it in a 50mL centrifuge tube, lyse it in a water bath at 70°C for more than 3h, and mix it every 20min Once, centrifuge at 10,000 rpm for 5 min at 4°C. The supernatant was extracted in phenol / chloroform to remove impurity proteins, and then an equal volume of isopropanol was added to the supernatant. After standing at -20°C for 30 minutes, centrifuge at 10,000 rpm for 10 minutes at 4°C. The supernatant was discarded, the precipitate was washed twice with 70% ethanol, dried in vacuo, dissolved in 100ul TE, and placed at -20°C for later use.

[0088] The degenerate primers P1, P2 were designed and synthesized according t...

Embodiment 3

[0096] Example 3 Preparation of recombinant β-glucosidase

[0097] The expression vector pPIC9 is subjected to double enzyme digestion (EcoR I+Not I), and simultaneously the gene BglA1 encoding β-glucosidase is subjected to double enzyme digestion (EcoR I+Not I), and the gene fragment encoding β-glucosidase is cut out and The expression vector pPIC9 was ligated to obtain the recombinant plasmid pPIC9-BglA1 containing the XH6 (Phialophora sp.) β-glucosidase gene BglA1 and transformed into Pichia pastoris GS115 to obtain the recombinant Pichia pastoris strain GS115 / BglA1.

[0098] The GS115 strain containing the recombinant plasmid was inoculated in 300 mL of BMGY culture medium, and cultured with shaking at 250 rpm at 30°C for 48 hours, and then the bacteria were collected by centrifugation. Then resuspend in 150mL BMMY medium, shake culture at 250rpm at 30°C. After 72 hours of induction, the supernatant was collected by centrifugation. The activity of β-glucosidase was deter...

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

PropertyMeasurementUnit
molecular weightaaaaaaaaaa
Login to view more

Abstract

The invention relates to the field of genetic engineering, in particular to medium-temperature beta-glucosidase BglA1, gene of the same and application of the same. The novel medium-temperature beta-glucosidase BglA1 contains amino acid sequence shown like SEQ ID NO.1. The invention further provides the gene for encoding the medium-temperature beta-glucosidase BglA1, recombination carrier containing the gene, recombination bacterial strain containing the gene and application of the medium-temperature beta-glucosidase BglA1, wherein nucleotide sequence of the gene is shown like SEQ ID NO.2. The optimum potential of hydrogen (pH) of the medium-temperature beta-glucosidase BglA1 is 6.0 and has higher enzymatic activity when the pH is from 5.0 to 7.0. Optimum temperature of the medium-temperature beta-glucosidase BglA1 is 50 DEG C, thereby being good in heat resistance. Thus, the medium-temperature beta-glucosidase BglA1 can be applied to industrial production with requirements for heat resistance.

Description

technical field [0001] The invention relates to the field of genetic engineering, in particular, the invention relates to a mesophilic β-glucosidase BglA1 and its gene and application. Background technique [0002] The regeneration and degradation of biomass is an important link in nature. About 15% of the total carbon in nature is fixed by plants every year, and 50% of the fixed carbon forms structural polysaccharides and lignin. This part is usually called woody. cellulose. Lignocellulose is the most abundant biomass on Earth produced by plants through photosynthesis. Structurally, lignocellulose is a polymer composite composed of lignin, cellulose and hemicellulose. Cellulose accounts for about 40-45% of the dry weight of cells, and its structure is a linear structure molecule composed of glucose connected by β-1,4-glycosidic bonds (Martinez AT, Ruiz-Duenas FJ, Martinez MJ, et al. (2009) Enzymatic delignification of plant cell wall: from nature to mill. Curr Opin Biote...

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 Applications(China)
IPC IPC(8): C12N9/42C12N15/56C12N15/63C12N15/81C12N1/19C12N1/14C12R1/645C12R1/84
Inventor 詹志春张菁
Owner WUHAN SUNHY BIOLOGICAL
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