Chlorpyrifos degrading bacteria and application thereof
A technology for degrading bacteria and colonies of chlorpyrifos, which can be applied to bacteria, microorganisms, biochemical equipment and methods, etc., and can solve problems such as limited means, low efficiency, and secondary pollution.
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Embodiment 1
[0021] Embodiment one: Erwinia xishuaiensis SCU-B244 T screening and separation
[0022] The cricket samples used in the experiment are adults of Gryllus chinensis, which are mostly distributed in farmland. They were captured in batches in August 2012 from the wasteland of Jiang’an Campus, Sichuan University, Shuangliu County, Chengdu, Sichuan (30°33’ 38.04”North 104°00 '20.17” East, 481 meters above sea level). After the microorganisms were eluted from the crickets with sterile water, they were spread on TSB, Chase, Gao’s No. 1, PDA, beef extract peptone and parasite inorganic salt medium by the dilution plate method, and cultivated at 37°C until visible Colonies appeared, and were identified after purification.
[0023] Description of strains:
[0024] Gram-negative bacteria, facultative aerobic, cream-colored colonies. Oxidase negative, catalase positive. The pH growth range is 6 to 9, and the optimum growth salt concentration is 1% to 2%. The bacteria has alkaline ...
Embodiment 2
[0025] Embodiment two: Erwinia xishuaiensis SCU-B244 T multiphase taxonomic identification of
[0026] the strain Erwinia xishuaiensis SCU-B244 T Biolog automatic bacterial identification system was used for carbon source utilization, fatty acid composition was determined by GC-MS analysis, enzymatic properties were identified by API ZYM reagent strips, acid production was identified by API50CHE reagent strips, and the reference strain was Erwinia oleae DSM 23398 T . Carbon source utilization was determined by Biolog automatic bacterial identification system. The result is as follows:
[0027] Available carbon sources: dextrin, N-acetyl-D-glucosamine, L-arabinose, D-fructose, D-galactose, α-D-glucose, maltose, D-mannitol, D-mannose, D-melibiose, β-methyl-D-glucoside, allulose L-raffinose, D-trehalose, turanose, methylpyruvate, citric acid, formic acid, D-lactobionic acid Esters, D-galacturonic acid, D-gluconic acid, p-hydroxyphenylacetic acid, α-ketoglutaric acid, ...
Embodiment 3
[0035] Example 3: 16S rDNA sequencing and evolutionary tree construction
[0036] The total bacterial DNA was extracted by SDS method, the 16S rRNA gene sequence of the strain was amplified by PCR method, and the DNA sequencing was completed by Shanghai Sangon Bioengineering Technology Service Co., Ltd. Go to the GenBank (http: / / www.ncbi.nlm.nih.gov / ) database to submit the partial sequence of the 16S rRNA gene measured by each strain for registration to obtain the sequence number. Then perform BLAST comparison on NCBI (National Center for Biotechnology Information) to find the strain with the closest relationship. The sequences of the corresponding strains with the closest relatives were compared by BioEdit, and then the phylogenetic tree was constructed using the Neighbor-Joinin (N-J) method on the software MEGA 5.0. The corresponding primers, reaction system and conditions for PCR are as follows:
[0037] Primer PA8: 5'-CCGTCGACGAGCTCAGAGTTTGATCCTGGCTCAG-3' and PB1: 5'-CC...
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