Use of green fluorescent protein gene to label Bacillus subtilis strains.
Weifeng Shen, Baolong Niu, Weng Hongbiao, Yan Liu, Lihua He, Zhiqi Meng
Abstract
Weifeng Shen, Baolong Niu, Weng Hongbiao, Yan Liu, Lihua He, Zhiqi Meng
Abstract
The xylR promoter from B.subtilis 168 chromosomal DNA was ligated with GFP gene from plasmid GFPuv.The expression fragment xylR-GFP was inserted into the shuttle-vector pIM.The recombinant vector pIM-GFP was successfully obtained.The pIM-GFP was transformed into BS523 strain.Transformants were identified by green fluorescence observation with microscope.The results showed that pIM-GFP was successfully integrated into the strain BS523.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
The xylR promoter from B.subtilis 168 chromosomal DNA was ligated with GFP gene from plasmid GFPuv.The expression fragment xylR-GFP was inserted into the shuttle-vector pIM.The recombinant vector pIM-GFP was successfully obtained.The pIM-GFP was transformed into BS523 strain.Transformants were identified by green fluorescence observation with microscope.The results showed that pIM-GFP was successfully integrated into the strain BS523.
Key concepts: Green fluorescent protein, Bacillus subtilis, Shuttle vector, Plasmid, Gene, Fluorescence microscope, Recombinant DNA, Molecular biology