Literature DB >> 23672214

Kinetic characterization of hydrolysis of nitrocefin, cefoxitin, and meropenem by β-lactamase from Mycobacterium tuberculosis.

Carmen Chow1, Hua Xu, John S Blanchard.   

Abstract

The constitutively expressed, chromosomally encoded β-lactamase (BlaC) is the enzyme responsible for the intrinsic resistance to β-lactam antibiotics in Mycobacterium tuberculosis. Previous studies from this laboratory have shown that the enzyme exhibits an extended-spectrum phenotype, with very high levels of penicillinase and cephalosporinase activity, as well as weak carbapenemase activity [Tremblay, L. W., et al. (2008) Biochemistry 47, 5312-5316]. In this report, we have determined the pH dependence of the kinetic parameters, revealing that the maximal velocity depends on the ionization state of two groups: a general base exhibiting a pK value of 4.5 and a general acid exhibiting a pK value of 7.8. Having defined a region where the kinetic parameters are pH-independent (pH 6.5), we determined solvent kinetic isotope effects (SKIEs) for three substrates whose kcat values differ by 5.5 orders of magnitude. Nitrocefin is a highly activated, chromogenic cephalosporin derivative that exhibits steady-state solvent kinetic isotope effects of 1.4 on both V and V/K. Cefoxitin is a slower cephalosporin derivative that exhibits a large SKIE on V of 3.9 but a small SKIE of 1.8 on V/K in steady-state experiments. Pre-steady-state, stopped-flow experiments with cefoxitin revealed a burst of β-lactam ring opening with associated SKIE values of 1.6 on the acylation step and 3.4 on the deacylation step. Meropenem is an extremely slow substrate for BlaC and exhibits burst kinetics in the steady-state experiments. SKIE determinations with meropenem revealed large SKIEs on both the acylation and deacylation steps of 3.8 and 4.0, respectively. Proton inventories in all cases were linear, indicating the participation of a single solvent-derived proton in the chemical step responsible for the SKIE. The rate-limiting steps for β-lactam hydrolysis of these substrates are analyzed, and the chemical steps responsible for the observed SKIE are discussed.

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Year:  2013        PMID: 23672214      PMCID: PMC3750105          DOI: 10.1021/bi400177y

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  26 in total

1.  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

2.  Identification of beta-lactamases by analytical isoelectric focusing: correlation with bacterial taxonomy.

Authors:  M Matthew; A M Harris
Journal:  J Gen Microbiol       Date:  1976-05

3.  Pre-steady state beta-lactamase kinetics. The trapping of a covalent intermediate and the interpretation of pH rate profiles.

Authors:  E G Anderson; R F Pratt
Journal:  J Biol Chem       Date:  1983-11-10       Impact factor: 5.157

4.  An ultrahigh resolution structure of TEM-1 beta-lactamase suggests a role for Glu166 as the general base in acylation.

Authors:  George Minasov; Xiaojun Wang; Brian K Shoichet
Journal:  J Am Chem Soc       Date:  2002-05-15       Impact factor: 15.419

5.  Lysine-73 is involved in the acylation and deacylation of beta-lactamase.

Authors:  E J Lietz; H Truher; D Kahn; M J Hokenson; A L Fink
Journal:  Biochemistry       Date:  2000-05-02       Impact factor: 3.162

6.  Genetic and functional analysis of the chromosome-encoded carbapenem-hydrolyzing oxacillinase OXA-40 of Acinetobacter baumannii.

Authors:  Claire Héritier; Laurent Poirel; Daniel Aubert; Patrice Nordmann
Journal:  Antimicrob Agents Chemother       Date:  2003-01       Impact factor: 5.191

7.  Kinetics of turnover of cefotaxime by the Enterobacter cloacae P99 and GCl beta-lactamases: two free enzyme forms of the P99 beta-lactamase detected by a combination of pre- and post-steady state kinetics.

Authors:  Sanjai Kumar; S A Adediran; Michiyoshi Nukaga; R F Pratt
Journal:  Biochemistry       Date:  2004-03-09       Impact factor: 3.162

8.  Novel method for detection of beta-lactamases by using a chromogenic cephalosporin substrate.

Authors:  C H O'Callaghan; A Morris; S M Kirby; A H Shingler
Journal:  Antimicrob Agents Chemother       Date:  1972-04       Impact factor: 5.191

Review 9.  Reappraising the use of β-lactams to treat tuberculosis.

Authors:  Sebastian G Kurz; Robert A Bonomo
Journal:  Expert Rev Anti Infect Ther       Date:  2012-09       Impact factor: 5.091

10.  Penicillanic acid sulfone: an unexpected isotope effect in the interaction of 6 alpha- and 6 beta-monodeuterio and of 6,6-dideuterio derivatives with RTEM beta-lactamase from Escherichia coli.

Authors:  D G Brenner; J R Knowles
Journal:  Biochemistry       Date:  1981-06-23       Impact factor: 3.162

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2.  Mechanisms of proton relay and product release by Class A β-lactamase at ultrahigh resolution.

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Journal:  J Biol Chem       Date:  2019-07-21       Impact factor: 5.157

4.  Carbapenems and Rifampin Exhibit Synergy against Mycobacterium tuberculosis and Mycobacterium abscessus.

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Journal:  Antimicrob Agents Chemother       Date:  2015-08-10       Impact factor: 5.191

5.  Adding Insult to Injury: Mechanistic Basis for How AmpC Mutations Allow Pseudomonas aeruginosa To Accelerate Cephalosporin Hydrolysis and Evade Avibactam.

Authors:  Cole L Slater; Judith Winogrodzki; Pablo A Fraile-Ribot; Antonio Oliver; Mazdak Khajehpour; Brian L Mark
Journal:  Antimicrob Agents Chemother       Date:  2020-08-20       Impact factor: 5.191

6.  Phosphate Promotes the Recovery of Mycobacterium tuberculosis β-Lactamase from Clavulanic Acid Inhibition.

Authors:  Wouter Elings; Raffaella Tassoni; Steven A van der Schoot; Wendy Luu; Josef P Kynast; Lin Dai; Anneloes J Blok; Monika Timmer; Bogdan I Florea; Navraj S Pannu; Marcellus Ubbink
Journal:  Biochemistry       Date:  2017-11-14       Impact factor: 3.162

7.  Penicillin Binding Proteins and β-Lactamases of Mycobacterium tuberculosis: Reexamination of the Historical Paradigm.

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Journal:  mSphere       Date:  2022-02-23       Impact factor: 4.389

8.  Glby, Encoded by MAB_3167c, Is Required for In Vivo Growth of Mycobacteroides abscessus and Exhibits Mild β-Lactamase Activity.

Authors:  Christos Galanis; Emily C Maggioncalda; Pankaj Kumar; Gyanu Lamichhane
Journal:  J Bacteriol       Date:  2022-04-05       Impact factor: 3.476

9.  A Novel Metallo-β-Lactamase Involved in the Ampicillin Resistance of Streptococcus pneumoniae ATCC 49136 Strain.

Authors:  Chia-Yu Chang; Hui-Jen Lin; Bor-Ran Li; Yaw-Kuen Li
Journal:  PLoS One       Date:  2016-05-23       Impact factor: 3.240

10.  Application of the uridine auxotrophic host and synthetic nucleosides for a rapid selection of hydrolases from metagenomic libraries.

Authors:  Nina Urbelienė; Simonas Kutanovas; Rita Meškienė; Renata Gasparavičiūtė; Daiva Tauraitė; Martyna Koplūnaitė; Rolandas Meškys
Journal:  Microb Biotechnol       Date:  2018-10-09       Impact factor: 5.813

  10 in total

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