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Transformation of Bacillus amyloliquefaciens by electroporation

A method for transformation of whole Bacillus amyloliquefaciens cells by electroporation was developed. The procedure is as efficient as the protoplast transformation method, resulting in up to 105 transformants/μg plasmid DNA, but requires less effort and time. Cells for electroporation were grown...

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Published in:FEMS microbiology letters 1989-10, Vol.61 (1‐2), p.165-170
Main Author: VEHMAANPERA, J
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Language:English
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description A method for transformation of whole Bacillus amyloliquefaciens cells by electroporation was developed. The procedure is as efficient as the protoplast transformation method, resulting in up to 105 transformants/μg plasmid DNA, but requires less effort and time. Cells for electroporation were grown to late exponential phase in a rich medium supplemented with 0.25 M sucrose, washed with and resuspended in 0.25 M sucrose, 1 mM HEPES, 1 mM MgCl2, 10% (v/v) glycerol, pH 7.0, at 3–5 × 1010 cells/ml for storage at ‐80%°C. The highest transformation frequency was obtained at 7.5 kV/cm with a 25 μF capacitor. The transformation efficiency increased linearly with DNA concentration at least over the range 10 ng‐12.5 μg/ml. Transformations with ligated DNA and of industrial strains were also successful. In addition, B. subtilis cells treated as above could be transformed by electroporation, resulting in 104 transformants/μg DNA at 12.5 kV/cm.
doi_str_mv 10.1111/j.1574-6968.1989.tb03572.x
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The procedure is as efficient as the protoplast transformation method, resulting in up to 105 transformants/μg plasmid DNA, but requires less effort and time. Cells for electroporation were grown to late exponential phase in a rich medium supplemented with 0.25 M sucrose, washed with and resuspended in 0.25 M sucrose, 1 mM HEPES, 1 mM MgCl2, 10% (v/v) glycerol, pH 7.0, at 3–5 × 1010 cells/ml for storage at ‐80%°C. The highest transformation frequency was obtained at 7.5 kV/cm with a 25 μF capacitor. The transformation efficiency increased linearly with DNA concentration at least over the range 10 ng‐12.5 μg/ml. Transformations with ligated DNA and of industrial strains were also successful. 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The procedure is as efficient as the protoplast transformation method, resulting in up to 105 transformants/μg plasmid DNA, but requires less effort and time. Cells for electroporation were grown to late exponential phase in a rich medium supplemented with 0.25 M sucrose, washed with and resuspended in 0.25 M sucrose, 1 mM HEPES, 1 mM MgCl2, 10% (v/v) glycerol, pH 7.0, at 3–5 × 1010 cells/ml for storage at ‐80%°C. The highest transformation frequency was obtained at 7.5 kV/cm with a 25 μF capacitor. The transformation efficiency increased linearly with DNA concentration at least over the range 10 ng‐12.5 μg/ml. Transformations with ligated DNA and of industrial strains were also successful. 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Psychology</topic><topic>Microbiology</topic><topic>pC194</topic><topic>pE194</topic><topic>Plasmids</topic><topic>pUB110</topic><topic>transformation</topic><topic>Transformation, Bacterial</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>VEHMAANPERA, J</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>FEMS microbiology letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>VEHMAANPERA, J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Transformation of Bacillus amyloliquefaciens by electroporation</atitle><jtitle>FEMS microbiology letters</jtitle><addtitle>FEMS Microbiol Lett</addtitle><date>1989-10</date><risdate>1989</risdate><volume>61</volume><issue>1‐2</issue><spage>165</spage><epage>170</epage><pages>165-170</pages><issn>0378-1097</issn><eissn>1574-6968</eissn><coden>FMLED7</coden><abstract>A method for transformation of whole Bacillus amyloliquefaciens cells by electroporation was developed. The procedure is as efficient as the protoplast transformation method, resulting in up to 105 transformants/μg plasmid DNA, but requires less effort and time. Cells for electroporation were grown to late exponential phase in a rich medium supplemented with 0.25 M sucrose, washed with and resuspended in 0.25 M sucrose, 1 mM HEPES, 1 mM MgCl2, 10% (v/v) glycerol, pH 7.0, at 3–5 × 1010 cells/ml for storage at ‐80%°C. The highest transformation frequency was obtained at 7.5 kV/cm with a 25 μF capacitor. The transformation efficiency increased linearly with DNA concentration at least over the range 10 ng‐12.5 μg/ml. Transformations with ligated DNA and of industrial strains were also successful. 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identifier ISSN: 0378-1097
ispartof FEMS microbiology letters, 1989-10, Vol.61 (1‐2), p.165-170
issn 0378-1097
1574-6968
language eng
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source Alma/SFX Local Collection
subjects Bacillus - genetics
Bacillus - growth & development
Bacillus subtilis
Bacteriological methods and techniques used in bacteriology
Bacteriology
Biological and medical sciences
DNA
DNA, Bacterial - isolation & purification
Electrochemistry
Electropermeabilization
electroporation
Electro‐transformation
Fundamental and applied biological sciences. Psychology
Microbiology
pC194
pE194
Plasmids
pUB110
transformation
Transformation, Bacterial
title Transformation of Bacillus amyloliquefaciens by electroporation
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