Literature DB >> 9238058

A natural polymorphism in beta-lactamase is a global suppressor.

W Huang1, T Palzkill.   

Abstract

A M182T substitution was discovered as a second-site suppressor of a missense mutation in TEM-1 beta-lactamase. The combination of the M182T substitution with other substitutions in the enzyme indicates the M182T substitution is a global suppressor of missense mutations in beta-lactamase. The M182T substitution also is found in natural variants of TEM-1 beta-lactamase with altered substrate specificity that have evolved in response to antibiotic therapy. The M182T substitution may have been selected in natural isolates as a suppressor of folding or stability defects resulting from mutations associated with drug resistance. This pathway of protein evolution may occur in other targets of antimicrobial drugs such as the HIV protease.

Entities:  

Mesh:

Substances:

Year:  1997        PMID: 9238058      PMCID: PMC23137          DOI: 10.1073/pnas.94.16.8801

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  25 in total

1.  The structural stability of a protein is an important determinant of its proteolytic susceptibility in Escherichia coli.

Authors:  D A Parsell; R T Sauer
Journal:  J Biol Chem       Date:  1989-05-05       Impact factor: 5.157

Review 2.  Classification of beta-lactamases: groups 1, 2a, 2b, and 2b'.

Authors:  K Bush
Journal:  Antimicrob Agents Chemother       Date:  1989-03       Impact factor: 5.191

3.  Implication of Ile-69 and Thr-182 residues in kinetic characteristics of IRT-3 (TEM-32) beta-lactamase.

Authors:  S Farzaneh; E B Chaibi; J Peduzzi; M Barthelemy; R Labia; J Blazquez; F Baquero
Journal:  Antimicrob Agents Chemother       Date:  1996-10       Impact factor: 5.191

4.  Phage lambda repressor revertants. Amino acid substitutions that restore activity to mutant proteins.

Authors:  M H Hecht; R T Sauer
Journal:  J Mol Biol       Date:  1985-11-05       Impact factor: 5.469

5.  The release of enzymes from Escherichia coli by osmotic shock and during the formation of spheroplasts.

Authors:  H C Neu; L A Heppel
Journal:  J Biol Chem       Date:  1965-09       Impact factor: 5.157

6.  Rapid and efficient site-specific mutagenesis without phenotypic selection.

Authors:  T A Kunkel; J D Roberts; R A Zakour
Journal:  Methods Enzymol       Date:  1987       Impact factor: 1.600

Review 7.  Beta-lactamase inhibitors: another approach to overcoming antimicrobial resistance.

Authors:  R H Parker; M Eggleston
Journal:  Infect Control       Date:  1987-01

8.  Genetic analysis of staphylococcal nuclease: identification of three intragenic "global" suppressors of nuclease-minus mutations.

Authors:  D Shortle; B Lin
Journal:  Genetics       Date:  1985-08       Impact factor: 4.562

Review 9.  Guanidine hydrochloride denaturation studies of mutant forms of staphylococcal nuclease.

Authors:  D Shortle
Journal:  J Cell Biochem       Date:  1986       Impact factor: 4.429

10.  Mutator mutations in Escherichia coli induced by the insertion of phage mu and the transposable resistance elements Tn5 and Tn10.

Authors:  E C Siegel; S L Wain; S F Meltzer; M L Binion; J L Steinberg
Journal:  Mutat Res       Date:  1982-03       Impact factor: 2.433

View more
  60 in total

1.  A new TEM-derived extended-spectrum beta-lactamase (TEM-91) with an R164C substitution at the omega-loop confers ceftazidime resistance.

Authors:  Hiroshi Kurokawa; Naohiro Shibata; Yohei Doi; Keigo Shibayama; Kazunari Kamachi; Tetsuya Yagi; Yoshichika Arakawa
Journal:  Antimicrob Agents Chemother       Date:  2003-09       Impact factor: 5.191

2.  Identification and characterization of beta-lactamase inhibitor protein-II (BLIP-II) interactions with beta-lactamases using phage display.

Authors:  N G Brown; T Palzkill
Journal:  Protein Eng Des Sel       Date:  2010-03-22       Impact factor: 1.650

3.  Mistranslation drives the evolution of robustness in TEM-1 β-lactamase.

Authors:  Sinisa Bratulic; Florian Gerber; Andreas Wagner
Journal:  Proc Natl Acad Sci U S A       Date:  2015-09-21       Impact factor: 11.205

4.  SHV-129: A Gateway to Global Suppressors in the SHV β-Lactamase Family?

Authors:  Marisa L Winkler; Robert A Bonomo
Journal:  Mol Biol Evol       Date:  2015-11-03       Impact factor: 16.240

5.  Network Analysis of Sequence-Function Relationships and Exploration of Sequence Space of TEM β-Lactamases.

Authors:  Catharina Zeil; Michael Widmann; Silvia Fademrecht; Constantin Vogel; Jürgen Pleiss
Journal:  Antimicrob Agents Chemother       Date:  2016-04-22       Impact factor: 5.191

Review 6.  Epistasis in protein evolution.

Authors:  Tyler N Starr; Joseph W Thornton
Journal:  Protein Sci       Date:  2016-02-28       Impact factor: 6.725

7.  Unexpected enzyme TEM-126: role of mutation Asp179Glu.

Authors:  J Delmas; F Robin; F Bittar; C Chanal; R Bonnet
Journal:  Antimicrob Agents Chemother       Date:  2005-10       Impact factor: 5.191

8.  Novel TEM-type extended-spectrum beta-lactamase, TEM-134, in a Citrobacter koseri clinical isolate.

Authors:  Mariagrazia Perilli; Claudia Mugnaioli; Francesco Luzzaro; Marianna Fiore; Stefania Stefani; Gian Maria Rossolini; Gianfranco Amicosante
Journal:  Antimicrob Agents Chemother       Date:  2005-04       Impact factor: 5.191

Review 9.  Genetic constraints on protein evolution.

Authors:  Manel Camps; Asael Herman; Ern Loh; Lawrence A Loeb
Journal:  Crit Rev Biochem Mol Biol       Date:  2007 Sep-Oct       Impact factor: 8.250

10.  Evolution of New Delhi metallo-β-lactamase (NDM) in the clinic: Effects of NDM mutations on stability, zinc affinity, and mono-zinc activity.

Authors:  Zishuo Cheng; Pei W Thomas; Lincheng Ju; Alexander Bergstrom; Kelly Mason; Delaney Clayton; Callie Miller; Christopher R Bethel; Jamie VanPelt; David L Tierney; Richard C Page; Robert A Bonomo; Walter Fast; Michael W Crowder
Journal:  J Biol Chem       Date:  2018-06-16       Impact factor: 5.157

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.