Literature DB >> 1104589

Isolation and characterization of a new temperature-sensitive cell division mutant of Escherichia coli K-12.

D Santos, D F De Almeida.   

Abstract

A new temperature-sensitive mutant strain of Escherichia coli K-12 which forms filaments at 42 C has been described. The mutant, Y16, maintained growth and deoxyribonucleic acid synthesis at 42 C. The resulting multinucleate filaments gradually lost their viability at 42 C but could be recovered, even after 240 min of incubation, upon return to 30 C. Septation was resumed and growth was promptly re-established at normal rates. Recovery still took place in the presence of chloramphenicol added to the culture at the time of temperature shift from 42 to 30 C. A study has been made of the effects of adenine and various nucleosides on cultures of strain Y16 as compared with another filament-forming mutant, T44 tif-. Adenine (75 mug/ml), known to promote filamentation of strain T44 tif-, prevented the development of filaments and the loss of viability in cultures of Y16. Recovery of septation after temperature shift in cultures containing adenine presented a pattern similar to that found with the adenine-less cultures. Protection afforded by adenine at 42 C could be reversed by the addition of guanosine plus cytidine (100 mug/ml each). The effects of high concentrations of adenine and nucleosides on strain Y16 thus are the reverse of those observed with mutant T44 tif-. However, whereas tif-1 mutation promotes prophage induction at restrictive temperatures, no modification could be detected in the process of prophage induction in cultures of the lambda-lysogenic derivative of Y16 at 42 C, be it spontaneous or ultraviolet-mediated induction. The osmolarity increase afforded by 1% NaCl added to the medium did not alter the phenotype characteristics of strain Y16. The mutation has been mapped between argG and bgl. A close linkage has been observed between ftsH and argG, thereby locating the new mutation near 61 min on the map of E. coli chromosome, a previously undescribed region involved in cell division. The evidence reported indicates that strain Y16 differs in several respects from the already descirbed strains of the same class.

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Year:  1975        PMID: 1104589      PMCID: PMC236065          DOI: 10.1128/jb.124.3.1502-1507.1975

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  23 in total

1.  Prophage induction and cell division in E. coli. I. Further characterization of the thermosensitive mutation tif-1 whose expression mimics the effect of UV irradiation.

Authors:  M Castellazzi; J George; G Buttin
Journal:  Mol Gen Genet       Date:  1972

2.  Cell division in Escherichia coli: evidence for regulation of septation by effector molecules.

Authors:  D R Zusman; M Inouye; A B Pardee
Journal:  J Mol Biol       Date:  1972-08-14       Impact factor: 5.469

Review 3.  Linkage map of Escherichia coli strain K-12.

Authors:  A L Taylor; C D Trotter
Journal:  Bacteriol Rev       Date:  1972-12

4.  Process of cellular division in Escherichia coli: physiological study on thermosensitive mutants defective in cell division.

Authors:  M Ricard; Y Hirota
Journal:  J Bacteriol       Date:  1973-10       Impact factor: 3.490

5.  Initial characterization of temperature-sensitive cell division mutants of Escherichia coli.

Authors:  R G Allen; J A Smith; R C Knudsen; J R Walker
Journal:  Biochem Biophys Res Commun       Date:  1972-06-09       Impact factor: 3.575

6.  Mutant of Escherichia coli with thermosensitive protein in the process of cellular division.

Authors:  K Nagai; G Tamura
Journal:  J Bacteriol       Date:  1972-11       Impact factor: 3.490

Review 7.  Control of cell division in bacteria.

Authors:  M Slater; M Schaechter
Journal:  Bacteriol Rev       Date:  1974-06

8.  Rapid mapping of conditional and auxotrophic mutations in Escherichia coli K-12.

Authors:  B Low
Journal:  J Bacteriol       Date:  1973-02       Impact factor: 3.490

9.  Cell division and prophage induction in Escherichia coli: studies of nucleotide levels.

Authors:  W Ruff; E P Kirby; D A Goldthwait
Journal:  J Bacteriol       Date:  1971-06       Impact factor: 3.490

10.  Regulation of bacterial cell division: genetic and phenotypic analysis of temperature-sensitive, multinucleate, filament-forming mutants of Escherichia.

Authors:  J S Allen; C C Filip; R A Gustafson; R G Allen; J R Walker
Journal:  J Bacteriol       Date:  1974-03       Impact factor: 3.490

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  31 in total

1.  The FtsH protein accumulates at the septum of Bacillus subtilis during cell division and sporulation.

Authors:  W Wehrl; M Niederweis; W Schumann
Journal:  J Bacteriol       Date:  2000-07       Impact factor: 3.490

2.  GmFtsH9 expression correlates with in vivo photosystem II function: chlorophyll a fluorescence transient analysis and eQTL mapping in soybean.

Authors:  Zhitong Yin; Fanfan Meng; Haina Song; Xiaolin Wang; Maoni Chao; Guozheng Zhang; Xiaoming Xu; Dexiang Deng; Deyue Yu
Journal:  Planta       Date:  2011-06-03       Impact factor: 4.116

Review 3.  ATP-dependent proteinases in bacteria.

Authors:  O Hlavácek; L Váchová
Journal:  Folia Microbiol (Praha)       Date:  2002       Impact factor: 2.099

4.  FtsH is involved in the early stages of repair of photosystem II in Synechocystis sp PCC 6803.

Authors:  Paulo Silva; Elinor Thompson; Shaun Bailey; Olaf Kruse; Conrad W Mullineaux; Colin Robinson; Nicholas H Mann; Peter J Nixon
Journal:  Plant Cell       Date:  2003-09       Impact factor: 11.277

Review 5.  Regulated proteolysis in Gram-negative bacteria--how and when?

Authors:  Eyal Gur; Dvora Biran; Eliora Z Ron
Journal:  Nat Rev Microbiol       Date:  2011-10-24       Impact factor: 60.633

6.  Two ftsH-family genes encoded in the nuclear and chloroplast genomes of the primitive red alga Cyanidioschyzon merolae.

Authors:  R Itoh; H Takano; N Ohta; S Miyagishima; H Kuroiwa; T Kuroiwa
Journal:  Plant Mol Biol       Date:  1999-10       Impact factor: 4.076

7.  Escherichia coli mutant Y16 is a double mutant carrying thermosensitive ftsH and ftsI mutations.

Authors:  K J Begg; T Tomoyasu; W D Donachie; M Khattar; H Niki; K Yamanaka; S Hiraga; T Ogura
Journal:  J Bacteriol       Date:  1992-04       Impact factor: 3.490

Review 8.  Quality control of photosystem II: impact of light and heat stresses.

Authors:  Yasusi Yamamoto; Ryota Aminaka; Miho Yoshioka; Mahbuba Khatoon; Keisuke Komayama; Daichi Takenaka; Amu Yamashita; Nobuyoshi Nijo; Kayo Inagawa; Noriko Morita; Takayuki Sasaki; Yoko Yamamoto
Journal:  Photosynth Res       Date:  2008-10-21       Impact factor: 3.573

9.  AAA proteases with catalytic sites on opposite membrane surfaces comprise a proteolytic system for the ATP-dependent degradation of inner membrane proteins in mitochondria.

Authors:  K Leonhard; J M Herrmann; R A Stuart; G Mannhaupt; W Neupert; T Langer
Journal:  EMBO J       Date:  1996-08-15       Impact factor: 11.598

10.  A protease complex in the Escherichia coli plasma membrane: HflKC (HflA) forms a complex with FtsH (HflB), regulating its proteolytic activity against SecY.

Authors:  A Kihara; Y Akiyama; K Ito
Journal:  EMBO J       Date:  1996-11-15       Impact factor: 11.598

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