Abstract
Distributions of cell lengths in lexA+ and lexA mutant cultures during normal growth and under thymidine starvation conditions are presented. During normal growth lexA mutant cells were slightly shorter, on the average, than were lexA+ cells. lexA mutant cells were also shorter in comparison with lexA+ cells after a period of thymidine starvation. These results are consistent with the hypothesis that the lexA gene is involved in the coordination of cell division with DNA repair.
Full text
PDF

Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Howe W. E., Mount D. W. Analysis of cell division in single clones of the Escherichia coli K-12 lexA mutant. J Bacteriol. 1978 Mar;133(3):1278–1281. doi: 10.1128/jb.133.3.1278-1281.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Howe W. E., Mount D. W. Production of cells without deoxyribonucleic acid during thymidine starvation of lexA- cultures of Escherichia coli K-12. J Bacteriol. 1975 Dec;124(3):1113–1121. doi: 10.1128/jb.124.3.1113-1121.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mound D. W., Walker A. C., Kosel C. Suppression of lex mutations affecting deoxyribonucleic acid repair in Escherichia coli K-12 by closely linked thermosensitive mutations. J Bacteriol. 1973 Nov;116(2):950–956. doi: 10.1128/jb.116.2.950-956.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mount D. W., Kosel C. Ultraviolet light-induced mutation in UV-resistant, thermosensitive derivatives of lexA-strains of Escherichia coli K-12. Mol Gen Genet. 1975;136(2):95–106. doi: 10.1007/BF00272033. [DOI] [PubMed] [Google Scholar]
- Mount D. W., Low K. B., Edmiston S. J. Dominant mutations (lex) in Escherichia coli K-12 which affect radiation sensitivity and frequency of ultraviolet lght-induced mutations. J Bacteriol. 1972 Nov;112(2):886–893. doi: 10.1128/jb.112.2.886-893.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Witkin E. M. Ultraviolet mutagenesis and inducible DNA repair in Escherichia coli. Bacteriol Rev. 1976 Dec;40(4):869–907. doi: 10.1128/br.40.4.869-907.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
