Transformation of Streptomyces lincolnensis protoplasts with plasmid vectors
Language English Country United States Media print
Document type Journal Article
PubMed
1505879
DOI
10.1007/bf02933144
Knihovny.cz E-resources
- MeSH
- Transformation, Bacterial * MeSH
- Genetic Vectors MeSH
- Nucleic Acid Hybridization MeSH
- Plasmids * MeSH
- Protoplasts metabolism MeSH
- Blotting, Southern MeSH
- Streptomyces genetics growth & development MeSH
- Publication type
- Journal Article MeSH
A method for the preparation and regeneration of protoplasts of Streptomyces lincolnensis is described. Mycelium in the early exponential phase appeared to be most suitable for this purpose and yielded up to 25% regenerated intact cells. Transformation of S. lincolnensis protoplasts was achieved using broad-host-range streptomycete plasmid vectors pIJ622, pMP66, pRS410 and pIJ943 constructed from replicons pIJ101, pSLG33 and SCP2. The efficiency of transformation was 3.10(3) transformants per micrograms plasmid DNA when (2-5).10(7) recipient protoplasts were used. Interspecific transformations showed that there is no efficient restriction system in S. lincolnensis that would limit the transfer of genetic information from S. lividans or E. coli.
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J Bacteriol. 1985 Jul;163(1):180-5 PubMed
Nucleic Acids Res. 1987 Oct 12;15(19):8106 PubMed
Nature. 1980 Apr 10;284(5756):526-31 PubMed
Mol Gen Genet. 1982;185(2):223-8 PubMed
Folia Microbiol (Praha). 1990;35(5):456-9 PubMed
J Bacteriol. 1982 Aug;151(2):668-77 PubMed
J Gen Microbiol. 1981 Nov;127(1):137-46 PubMed
Gene. 1985;37(1-3):101-10 PubMed
Gene. 1985;35(3):223-35 PubMed
Biochemistry. 1985 Oct 22;24(22):6038-44 PubMed
Nature. 1980 Jul 31;286(5772):525-7 PubMed
Cell. 1984 Apr;36(4):1097-103 PubMed
J Gen Microbiol. 1989 Dec;135(12):3281-8 PubMed
Folia Microbiol (Praha). 1985;30(6):474-8 PubMed
Appl Environ Microbiol. 1986 Jan;51(1):126-31 PubMed
J Gen Microbiol. 1974 Feb;80(2):389-400 PubMed