Affiliation:
1. Institut für Biotechnologie, 1 des Forschungszentrums Jülich GmbH, Federal Republic of Germany.
Abstract
From a Corynebacterium glutamicum mutant possessing a homoserine dehydrogenase resistant to feedback inhibition by L-threonine, the corresponding gene (homFBR) was analyzed and compared with the wild-type hom gene. DNA fragment exchange experiments between both genes showed that a 0.23-kb region close to the 3' terminus of homFBR was responsible for deregulation. Nucleotide sequence analysis revealed a single transition from G to A in homFBR leading to replacement of glycine-378 by glutamate in the mutant homoserine dehydrogenase.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
49 articles.
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