Genetic mapping of regulatory mutations ofBacillus subtilis riboflavin operon

1990 ◽  
Vol 222 (2-3) ◽  
pp. 467-469 ◽  
Author(s):  
Rimma A. Kreneva ◽  
Daniel A. Perumov
Keyword(s):  
Genetic Mapping ◽  
Ofbacillus Subtilis ◽  
Regulatory Mutations ◽  
Riboflavin Operon

scholarly journals Genetic mapping of toxin regulatory mutations in Vibrio cholerae.

1979 ◽  
Vol 139 (3) ◽  
pp. 859-865 ◽  
Author(s):  
J J Mekalanos ◽  
R D Sublett ◽  
W R Romig
Keyword(s):  
Genetic Mapping ◽  
Vibrio Cholerae ◽  
Regulatory Mutations

Genetic Mapping in Experimental Populations

2013 ◽  
Author(s):  
J. W. Van Ooijen ◽  
J. Jansen
Keyword(s):  
Genetic Mapping ◽  
Experimental Populations

Phenotypic Characterization and Genetic Mapping of an Increased Stigma Mutant in Rice (Oryza sativa L.)

2011 ◽  
Vol 37 (10) ◽  
pp. 1779-1784
Author(s):  
Ming-Jing ZHOU ◽  
Yong WEN ◽  
Shuang-Cheng LI ◽  
Cheng-Bo LI ◽  
Man-Hua ZHANG ◽  
...  
Keyword(s):  
Oryza Sativa ◽  
Genetic Mapping ◽  
Oryza Sativa L ◽  
Phenotypic Characterization

scholarly journals Epr plays a key role in DegU-mediated swarming motility ofBacillus subtilis

2009 ◽  
Vol 295 (2) ◽  
pp. 187-194 ◽  
Author(s):  
Monica Gupta ◽  
Kestur Krishnamurthy Rao
Keyword(s):  
Ofbacillus Subtilis ◽  
Swarming Motility

scholarly journals Characterization and in Vivo Cloning of prlC, a Suppressor of Signal Sequence Mutations in Escherichia coli K12

Genetics ◽  
1987 ◽  
Vol 116 (4) ◽  
pp. 513-521
Author(s):  
Nancy J Trun ◽  
Thomas J Silhavy
Keyword(s):  
Escherichia Coli ◽  
Genetic Mapping ◽  
Signal Sequence ◽  
Illegitimate Recombination ◽  
Mutant Phenotype ◽  
E Coli ◽  
Physical Location ◽  
Sequence Deletion ◽  
New Alleles

ABSTRACT The prlC gene of E. coli was originally identified as an allele, prlC1, which suppresses certain signal sequence mutations in the genes for several exported proteins. We have isolated six new alleles of prlC that also confer this phenotype. These mutations can be placed into three classes based on the degree to which they suppress the lamBsignal sequence deletion, lamBs78. Genetic mapping reveals that the physical location of the mutations in prlC correlates with the strength of the suppression, suggesting that different regions of the gene can be altered to yield a suppressor phenotype. We also describe an in vivo cloning procedure using λplacMu9H. The procedure relies on transposition and illegitimate recombination to generate a specialized transducing phage that carries prlC1. This method should be applicable to any gene for which there is a mutant phenotype.

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