Bromopyruvate, an active site-directed inactivator of E. coli 2-keto-4-hydroxyglutarate(KHG) aldolase, modifies glutamic acid residue-45
Conference
·
· Fed. Proc., Fed. Am. Soc. Exp. Biol.; (United States)
OSTI ID:6179739
E. coli KHG-aldolase (2-keto-4-hydroxyglutarate in equilibrium pyruvate + glyoxylate), a novel trimeric Class I aldolase, requires one active-site lysine residue (Lys 133)/subunit for Schiff-base formation as well as one arginine residue (Arg 49)/subunit for catalytic activity. The substrate analog, 3-bromopyruvate (BRPY), causes a time- and concentration-dependent loss of KHG-aldolase activity. This inactivation is regarded as active site-directed since: (a) BRPY modification results in complete loss of enzymatic activity; (b) saturation kinetics are exhibited, suggesting that a reversible complex is formed between the aldolase and BRPY prior to the rate-limiting inactivation step; (c) over 90% of the initial aldolase activity is protected by either substrate, pyruvate or KHG; (d) 1.1 mol of /sup 14/C-BRPY is bound/enzyme subunit. Peptide isolation and sequencing show that the incorporated radioactivity is associated with residue Glu-45. Denaturation of the enzyme with guanidine x HCl following treatment with excess /sup 14/C-BRPY allows for the incorporation of carbon-14 at Cys-159 and Cys-180 as well. The presence of pyruvate protects Glu-45 from being esterified but does not prevent the alkylation of the two cysteine residues. These results suggest that Glu-45 is essential for the catalytic activity of E. coli KHG-aldolase, most likely functioning as the active-site amphoteric proton donor/acceptor moiety that is involved in the overall mechanism of the reaction catalyzed by this enzyme.
- Research Organization:
- Univ. of Michigan, Ann Arbor
- OSTI ID:
- 6179739
- Report Number(s):
- CONF-870644-
- Conference Information:
- Journal Name: Fed. Proc., Fed. Am. Soc. Exp. Biol.; (United States) Journal Volume: 46:6
- Country of Publication:
- United States
- Language:
- English
Similar Records
Active site studies of Escherichia coli 2-keto-4-hydroxyglutarate aldolase
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Identification of cofactor and herbicide binding domains in acetolactate synthase by bromopyruvate modification
Thesis/Dissertation
·
Wed Dec 31 23:00:00 EST 1986
·
OSTI ID:7140832
Alkylation of acetohydroxyacid synthase I from Escherichia coli K-12 by 3-bromopyruvate: evidence for a single active site catalyzing acetolactate and acetohydroxybutyrate synthesis
Journal Article
·
Mon Jun 01 00:00:00 EDT 1987
· J. Bacteriol.; (United States)
·
OSTI ID:6501645
Identification of cofactor and herbicide binding domains in acetolactate synthase by bromopyruvate modification
Conference
·
Fri May 01 00:00:00 EDT 1987
· Fed. Proc., Fed. Am. Soc. Exp. Biol.; (United States)
·
OSTI ID:6126581
Related Subjects
550201* -- Biochemistry-- Tracer Techniques
59 BASIC BIOLOGICAL SCIENCES
ALDEHYDE-LYASES
ALDOLASE
ALKYLATION
AMINO ACID SEQUENCE
AMINO ACIDS
BACTERIA
BIOCHEMICAL REACTION KINETICS
CARBON 14 COMPOUNDS
CARBON-CARBON LYASES
CARBOXYLIC ACIDS
CHEMICAL REACTIONS
DOSE-RESPONSE RELATIONSHIPS
ENZYME ACTIVITY
ENZYME INHIBITORS
ENZYMES
ESCHERICHIA COLI
GLUTAMIC ACID
IMINES
ISOTOPE APPLICATIONS
KINETICS
LABELLED COMPOUNDS
LYASES
MICROORGANISMS
MOLECULAR STRUCTURE
ORGANIC ACIDS
ORGANIC COMPOUNDS
ORGANIC NITROGEN COMPOUNDS
REACTION KINETICS
RESIDUES
SCHIFF BASES
TIME DEPENDENCE
TRACER TECHNIQUES
59 BASIC BIOLOGICAL SCIENCES
ALDEHYDE-LYASES
ALDOLASE
ALKYLATION
AMINO ACID SEQUENCE
AMINO ACIDS
BACTERIA
BIOCHEMICAL REACTION KINETICS
CARBON 14 COMPOUNDS
CARBON-CARBON LYASES
CARBOXYLIC ACIDS
CHEMICAL REACTIONS
DOSE-RESPONSE RELATIONSHIPS
ENZYME ACTIVITY
ENZYME INHIBITORS
ENZYMES
ESCHERICHIA COLI
GLUTAMIC ACID
IMINES
ISOTOPE APPLICATIONS
KINETICS
LABELLED COMPOUNDS
LYASES
MICROORGANISMS
MOLECULAR STRUCTURE
ORGANIC ACIDS
ORGANIC COMPOUNDS
ORGANIC NITROGEN COMPOUNDS
REACTION KINETICS
RESIDUES
SCHIFF BASES
TIME DEPENDENCE
TRACER TECHNIQUES