Method for transforming Bacillus siamensis by electric shock
A Bacillus and electric shock transformation technology, applied in the field of microbial genetic engineering, can solve the problems of low transformation efficiency, no reports, low cell membrane permeability, etc., and achieve the effects of simple operation, stable effect and high transformation rate
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Embodiment 1
[0118] 1. Instrument or equipment:
[0119] pH meter PB-10 was purchased from Sartorius; biochemical incubator SPX-158L was purchased from Ningbo Xinzhi, China; Eppendorf centrifuge 5418 was purchased from Eppendorf; steam sterilizer YXQ50 was purchased from Xi’an Taikang; ultra-clean workbench SKJH -1109 was purchased from Shanghai Sukun; double-beam UV-visible spectrophotometer UV2310II was purchased from Hangzhou Aosheng; Nano Drop spectrophotometer ND-1000 was purchased from Nano Drop Company; electric shock conversion instrument MicroPulser was purchased from Bio-Red, USA.
[0120] 2. Strains, plasmids and primers:
[0121] Bacillus siamese JFL15 is isolated from fish intestines and has strong antibacterial activity against a variety of pathogenic bacteria and fungi. It is preserved in the Institute of Food Biotechnology, School of Food Science, South China Agricultural University, and has undergone whole genome sequencing (Genbank accession number: NZ_KQ236689 .1).
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Embodiment 2
[0156] The difference between this example and Example 1 is that the shuttle vector used is the pHT08-cody-up-down homologous recombination plasmid, and the rest are the same as Example 1.
[0157] The successfully constructed pHT08-cody-up-down plasmid was transformed into Bacillus siamese JFL15 by electroporation, and the results were as follows: Figure 7 As shown, a large number of transformants grew on the LB resistance plate containing 5 μg / mL chloramphenicol, indicating that the plasmid pHT08-cody-up-down may have successfully transformed Bacillus siamese JFL15, and the plasmid pHT08-cody-up- The transformation efficiency of down was significantly higher than that of plasmid pHT08-cas9-gRNA. Randomly pick 3 transformants in LB liquid medium containing 5 μg / mL chloramphenicol resistance, after overnight culture, extract the plasmid, the results are as follows Figure 8 As shown, the plasmid band is between 8000 and 15000 bp, which is consistent with the expected size of...
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