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A strain of Bacillus licheniformis utm104 producing pyrethroid hydrolase and its application

A technology of Bacillus licheniformis and UTM104, applied in the field of fermentation, can solve problems such as pesticide residues and health threats, and achieve the effects of excellent strain performance, food safety, and social and economic benefits.

Active Publication Date: 2017-05-24
大地绿源环保科技(北京)有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

On the other hand, while the use of pesticides increases the yield of crops, it also causes pesticide residues in food and soil, causing various food safety problems and posing a huge threat to people's health.

Method used

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  • A strain of Bacillus licheniformis utm104 producing pyrethroid hydrolase and its application
  • A strain of Bacillus licheniformis utm104 producing pyrethroid hydrolase and its application
  • A strain of Bacillus licheniformis utm104 producing pyrethroid hydrolase and its application

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0032] The isolation and identification of embodiment 1 Bacillus licheniformis UTM104

[0033] Take about 1 gram of Tengchong hot spring bottom mud sample and place it in a 250ml Erlenmeyer flask filled with multiple small glass beads and 100ml sterile water, and incubate with shaking at 40°C for 1 hour at a speed of 160 rpm, then let it stand for 30 minutes. Draw 1ml of the supernatant under sterile conditions and insert it into 100ml of sterilized enrichment medium (15.0g colloidal chitin, 5.0g yeast powder, (NH 4 ) 2 SO 4 1.0g, MgSO 4 ·5H 2 O 0.3g, KH 2 PO 4 1.36 g, 1000 ml of water, pH 4.5), shake culture at 40° C. for 3 days, and rotate at 160 rpm. Take 1ml of the bacterial solution cultured for 3 days, add it to a test tube filled with 9ml sterile water, and prepare 10% by 10-fold dilution method. -1 , 10 -2 , 10 -3 , 10 -4 , 10 -5 , 10 -6 , 10 -7 the dilution. Take 0.1ml and spread on three solid medium plates containing colloidal chitin (15.0g colloidal c...

Embodiment 2

[0037] Example 2 Detection of Chitinase Activity of Bacterial Strain UTM104 and its Gene Sequence

[0038] The UTM104 strain was inoculated on the colloidal chitin solid medium plate of Example 1, and cultured at 37° C. for 3 days. It was observed to have a transparent chitinase hydrolysis circle. Primers chitinase-f: 5'-TCATCG GCT ACT ATC C-3' and chitinase-r: 5'-TCA CCG GAT TGA TCA G-3' designed according to the chitinase gene, and use the strain UTM104DNA of the present invention as a template , PCR amplification reaction, PCR reaction program: 95 ° C pre-denaturation for 5 minutes, 95 ° C denaturation for 30 seconds, 56 ° C annealing for 45 seconds, 72 ° C extension for 90 seconds, 35 cycles, 72 ° C extension for 10 minutes, detected by electrophoresis A nucleotide fragment with a size of about 1.7 kb was obtained, sequenced and sequenced in the NCBI GenBank database using the Blast program to obtain the sequence fragment encoding a chitinase gene, and its gene sequence i...

Embodiment 3

[0039] Example 3 Detection of cellulase activity of bacterial strain UTM104 and related gene sequences

[0040] The UTM104 strain was planted in sodium carboxymethyl cellulose medium (sodium carboxymethyl cellulose 5g, KH 2 PO 4 lg, agar 17g, NaNO 3 3g, KCL 0.5g, MgSO 4 0.5g, FeSO 4 0.01g, 1000ml of distilled water, pH 5.5~6.0), cultured at 40°C for 48 hours, stained with 0.2% Congo red for 30 minutes, washed the dye solution with distilled water, soaked in NaCl with a concentration of 1mol / L for 1 hour, and finally used 5% acetic acid fixes the color. The formation of a colorless transparent circle around the colony indicates that the bacterium secretes cellulase. Cellulase is a multi-enzyme mixture consisting of cellobiase, endo-β-glucanase and the like.

[0041] Primer betaglu-f: 5'-AAC GGT CCG CAT CAT C-3' and betaglu-r: 5'-CGA GGA AGA TGC CGA T-3' were designed according to the endo-β-glucanase gene, with the strain of the present invention UTM104DNA was used as a ...

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Abstract

The invention provides a Bacillus licheniformis UTM104 strain producing pyrethroid hydrolase and application thereof. The biological deposit number of the bacterium is CGMCC No.9509. UTM104 strain can carry out aerobic composting fermentation in organic solid waste such as sewage sludge, domestic garbage, animal carcasses, livestock and poultry manure, crop straw, etc., and form a stable colony ecosystem in organic materials, multiply rapidly in large numbers, and effectively degrade organic matter. The organic matter in the solid waste can be quickly reduced and made harmless; at the same time, the organic solid waste can be converted into biological fertilizer by using the microbial agent prepared by the invention. The UTM104 strain can also degrade pyrethroid pesticide residues on soil and plants, thereby ensuring food safety. The strain of the invention has excellent performance and has good social and economic benefits.

Description

technical field [0001] The invention relates to the field of fermentation, in particular to a Bacillus licheniformis UTM104 strain carrying a pyrethroid hydrolase gene and its application in degrading urban and rural organic solid waste and preparing biological fertilizers. Background technique [0002] At present, the organic solid waste produced by agricultural and animal husbandry production has become an important source of urban and rural environmental pollution. The annual large-scale production of crop straw and livestock manure and other waste not only causes farmland occupation, soil and groundwater pollution, but also produces odor pollution. Air. On the other hand, while the use of pesticides increases the yield of crops, it also causes pesticide residues in food and soil, causing various food safety problems and posing a huge threat to people's health. How to effectively remove agricultural products and pesticide residues in soil has become a widely concerned is...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C12N1/20C05F17/00C12R1/10
CPCC05F11/08C05F17/00C12N1/20C12N1/205C12R2001/10Y02W30/40
Inventor 刘永跃何璧梅许宜北汪涌
Owner 大地绿源环保科技(北京)有限公司