Literature DB >> 3493768

Carboxy groups as essential residues in beta-lactamases.

C Little, E L Emanuel, J Gagnon, S G Waley.   

Abstract

Beta-lactamases are divided into classes A, B and C on the basis of their amino acid sequences. Beta-Lactamases were incubated at pH 4.0 with the carboxy-group reagent 1-(3-dimethylaminopropyl)-3-ethylcarbodi-imide plus a coloured nucleophile and the extents of inactivation and nucleophile incorporation were monitored. Two class A enzymes (from Bacillus cereus and Bacillus licheniformis) and two class C enzymes (from Enterobacter cloacae P99 and Pseudomonas aeruginosa) were examined. All four enzymes were inactivated, with total inactivation corresponding to the incorporation of approx. 2-3 mol of nucleophile/mol of enzyme. In the case of beta-lactamase I from Bacillus cereus, some 53% of the incorporated nucleophile was located on glutamic acid-168 in the amino acid sequence.

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Year:  1986        PMID: 3493768      PMCID: PMC1147395          DOI: 10.1042/bj2400215

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  19 in total

1.  Beta-lactamase (Enterobacter species).

Authors:  G W Ross
Journal:  Methods Enzymol       Date:  1975       Impact factor: 1.600

2.  Relation between modification of functional groups of proteins and their biological activity. I.A graphical method for the determination of the number and type of essential groups.

Authors:  C L TSOU
Journal:  Sci Sin       Date:  1962-11

3.  A method for characterizing the type and numbers of groups involved in enzyme action.

Authors:  W J RAY; D E KOSHLAND
Journal:  J Biol Chem       Date:  1961-07       Impact factor: 5.157

4.  Modification of the essential carboxyl group in octopine dehydrogenase.

Authors:  C Huc; A Olomucki; F Thomé-Beau
Journal:  FEBS Lett       Date:  1975-12-15       Impact factor: 4.124

5.  The pH-dependence and group modification of beta-lactamase I.

Authors:  S G Waley
Journal:  Biochem J       Date:  1975-09       Impact factor: 3.857

6.  Chemical studies on methionyl-tRNA synthetase from Escherichia coli.

Authors:  C J Bruton; B S Hartley
Journal:  J Mol Biol       Date:  1970-09-14       Impact factor: 5.469

7.  The structure of beta-lactamases.

Authors:  R P Ambler
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  1980-05-16       Impact factor: 6.237

8.  Mutant of Pseudomonas aeruginosa 18S that synthesizes type Id beta-lactamase constitutively.

Authors:  F Flett; N A Curtis; M H Richmond
Journal:  J Bacteriol       Date:  1976-09       Impact factor: 3.490

9.  ampC cephalosporinase of Escherichia coli K-12 has a different evolutionary origin from that of beta-lactamases of the penicillinase type.

Authors:  B Jaurin; T Grundström
Journal:  Proc Natl Acad Sci U S A       Date:  1981-08       Impact factor: 11.205

10.  Separation, purification and properties of beta-lactamase I and beta-lactamase II from Bacillus cereus 569/H/9.

Authors:  R B Davies; E P Abraham
Journal:  Biochem J       Date:  1974-10       Impact factor: 3.857

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  3 in total

1.  Inactivation of the RTEM-1 cysteine beta-lactamase by iodoacetate. The nature of active-site functional groups and comparisons with the native enzyme.

Authors:  A K Knap; R F Pratt
Journal:  Biochem J       Date:  1991-01-01       Impact factor: 3.857

2.  beta-lactamase I from Bacillus cereus. Structure and site-directed mutagenesis.

Authors:  P J Madgwick; S G Waley
Journal:  Biochem J       Date:  1987-12-15       Impact factor: 3.857

3.  The active-site-serine penicillin-recognizing enzymes as members of the Streptomyces R61 DD-peptidase family.

Authors:  B Joris; J M Ghuysen; G Dive; A Renard; O Dideberg; P Charlier; J M Frère; J A Kelly; J C Boyington; P C Moews
Journal:  Biochem J       Date:  1988-03-01       Impact factor: 3.857

  3 in total

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