Literature DB >> 3491214

Amber mutants in gene 67 of phage T4. Effects on formation and shape determination of the head.

B Keller, M Maeder, C Becker-Laburte, E Kellenberger, T A Bickle.   

Abstract

Two amber mutations in gene 67 of bacteriophage T4 were constructed by oligonucleotide-directed mutagenesis and the resulting mutated genes were recombined back into the phage genome and their phenotype was studied. The 67amK1 mutation is close to the amino terminus of the gene, and phage carrying this mutation are unable to form plaques on suppressor-negative hosts. A second mutation, 67amK2, which lies in the middle of the gene, three codons N-terminal to a proteolytic cleavage site, produces a small number of viable phage particles. In suppressor-negative hosts, both mutants produce polyheads and proheads. 67amK1 assembles only few proheads that have a disorganized core structure, as judged from thin sections of infected cells. The proheads and the mature phages of both mutants are mainly isometric rather than having the usual prolate shape. Depending on the 67 mutant and the host, between 20% and 73% of the particles that are produced are isometric, and 1 to 10% are two-tailed biprolate particles. 67amK2 phages grown on a supD suppressor strain that inserts serine in place of the wild-type leucine do not contain gp67* derived from gene product 67 (gp67) by proteolytic cleavage. This demonstrates the importance of the correct amino acid at this position in the protein. Other abnormalities in these 67amK2 phages are the presence of uncleaved scaffolding core proteins (IPIII and gp68), indicating a structural alteration in the prohead scaffold, resulting in only partial cleavage. In wild-type phages these proteins are found in the head only in the cleaved form. With double-mutants of 67 with mutations in the major shell protein gp23 no naked scaffolding cores were found, confirming the necessity of gp67 for the assembly or persistence of a "normal" core.

Entities:  

Mesh:

Substances:

Year:  1986        PMID: 3491214     DOI: 10.1016/0022-2836(86)90077-x

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  7 in total

Review 1.  Bacteriophage T4 genome.

Authors:  Eric S Miller; Elizabeth Kutter; Gisela Mosig; Fumio Arisaka; Takashi Kunisawa; Wolfgang Rüger
Journal:  Microbiol Mol Biol Rev       Date:  2003-03       Impact factor: 11.056

2.  Length and shape variants of the bacteriophage T4 head: mutations in the scaffolding core genes 68 and 22.

Authors:  B Keller; J Dubochet; M Adrian; M Maeder; M Wurtz; E Kellenberger
Journal:  J Virol       Date:  1988-08       Impact factor: 5.103

3.  Analysis of the open reading frames of the main capsid proteins of actinophage VWB.

Authors:  J Anné; P Fiten; L Van Mellaert; B Joris; G Opdenakker; H Eyssen
Journal:  Arch Virol       Date:  1995       Impact factor: 2.574

4.  Prohead core of bacteriophage T4 can act as an intermediate in the T4 head assembly pathway.

Authors:  A Kuhn; B Keller; M Maeder; F Traub
Journal:  J Virol       Date:  1987-01       Impact factor: 5.103

5.  The delta domain of the HK97 major capsid protein is essential for assembly.

Authors:  Bonnie Oh; Crystal L Moyer; Roger W Hendrix; Robert L Duda
Journal:  Virology       Date:  2014-04-10       Impact factor: 3.616

6.  A Cut above the Rest: Characterization of the Assembly of a Large Viral Icosahedral Capsid.

Authors:  Erin R Reilly; Milky K Abajorga; Cory Kiser; Nurul Humaira Mohd Redzuan; Zein Haidar; Lily E Adams; Randy Diaz; Juliana A Pinzon; André O Hudson; Lindsay W Black; Ru-Ching Hsia; Susan T Weintraub; Julie A Thomas
Journal:  Viruses       Date:  2020-07-05       Impact factor: 5.048

Review 7.  T4 genes in the marine ecosystem: studies of the T4-like cyanophages and their role in marine ecology.

Authors:  Martha R J Clokie; Andrew D Millard; Nicholas H Mann
Journal:  Virol J       Date:  2010-10-28       Impact factor: 4.099

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.