Affiliation:
1. Laboratório de Genetica Molecular, Instituto Gulbenkian de Ciência, Oeiras, Portugal.
Abstract
Two recombinant plasmids, pSNL1 and pSNL2, carrying structural genes for L-arabinose utilization were isolated from a Bacillus subtilis gene library. Both plasmids complemented araD mutations in a Rec- B. subtilis strain and in Escherichia coli. Moreover, pSNL1 also complemented araB mutations in both species and efficiently transformed araA Rec+ B. subtilis strains to Ara+. Detailed physical mapping of both plasmids in addition to transformation experiments involving defined restriction fragments from the pSNL1 insert unambiguously determined the gene order to be araD, araB, and araA, an order different from that found in E. coli.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Reference9 articles.
1. Metabolic and nutritional factor influencing the development of competence for transfection of Bacillus subtilis;Bott K. F.;Bacteriol. Rev.,1968
2. Facile in vivo transfer of mutation between the Bacillus subtilis chromosome and a plasmid harbouring homologous DNA;Chak K. F.;J. Gen. Microbiol.,1982
3. Cloning of the SacS gene encoding a positive regulator of the sucrose regulon in Bacillus subtilis;Debarbouill M.;FEMS Microbiol. Lett.,1987
4. Plasmid transformation in Bacillus subtilis. Alterations introduced into the recipient-homologous DNA can be corrected in transformation;Iglesias A.;Mol. Gen. Genet.,1981
5. Metabolisme du Larabinose chez Bacillus subtilis Marburg Ind- 168;Lepesant J. A.;C. R. Acad. Sci. Ser. D,1967
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