A mutation affecting alanine-alpha-ketoisovalerate transaminase activity has been shown to be cotransducible with ilv gene cluster. The transaminase deficiency results in conditional isoleucine auxotrophy in the presence of alanine.
A mutation leading to the total lack of nitrite reductase activity in Escherichia coli K 12
✍ Scribed by Chippaux, M. ;Giudici, D. ;Abou-Jaoudé, A. ;Casse, F. ;Pascal, M. C.
- Publisher
- Springer
- Year
- 1978
- Tongue
- English
- Weight
- 441 KB
- Volume
- 160
- Category
- Article
- ISSN
- 0026-8925
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✦ Synopsis
Mutants of E. coli, completely devoid of nitrite reductase activity with glucose or formate as donor were studied. Biochemical analysis indicates that they are simultaneously affected in nitrate reductase, nitrite reductase, fumarate reductase and hydrogenase activities as well as in cytochrome C552 biosynthesis. The use of an antiserum specific for nitrate reductase shows that the nitrate reductase protein is probably missing. A single mutation is responsible for this phenotype: the gene affected, nir R, is located close to tyr R i.e. at 29 min on the chromosomal map.
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