Literature DB >> 11736656

Allosteric behaviour of 1:5 hybrids of mutant subunits of Clostridium symbiosum glutamate dehydrogenase differing in their amino acid specificity.

A Goyal1, X G Wang, P C Engel.   

Abstract

Hybrid hexamers were made by refolding mixtures of two mutant forms of clostridial glutamate dehydrogenase. Mutant Cys320Ser (C320S) has a similar activity to the wild-type enzyme, but is unreactive with Ellman's reagent, 5,5'-dithiobis(2-nitrobenzoate) (DTNB). The triple mutant Lys89Leu/Ala163Gly/Ser380Ala (K89L/A163G/S380A), active with norleucine but not glutamate, is inactivated by DTNB, since the amino acid residue at position 320 is a cysteine residue. The chosen ratio favoured 1:5 hybrids of the triple mutant and C320S. The renatured mixture was treated with DTNB and separated on an NAD(+)-agarose column to which only C320S subunits bind tightly. Fractions were monitored for glutamate and norleucine activity and for releasable thionitrobenzoate to establish subunit stoichiometry. A fraction highly enriched in the 1:5 hybrid was identified. Homohexamers (C320S with 40 mM glutamate and 1 mM NAD(+) at pH 8.8, or K89L/A163G/S380A with 70 mM norleucine and 1 mM NAD(+) at pH 8.5) showed allosteric activation; succinate activated C320S approx. 50-fold (EC(50)=70 mM, h=2.4), and glutarate gave approx. 30-fold activation (EC(50)=35 mM, h=2.3). For the triple mutant, corresponding values were 80 mM and 2.2 for succinate, and 75 mM and 1.7 for glutarate, but maximal activation was only about 2-fold. In the 1:5 hybrid, with only one norleucine-active subunit per hexamer, responses to glutarate and succinate were still co-operative, and activation was more extensive than in the triple mutant homohexamer. A single norleucine-active subunit can thus respond co-operatively to a substrate analogue at the other five inactive sites. On the other hand, similar hyperbolic dependence on the norleucine concentration for the hybrid and the triple mutant homohexamer reflected the inability of C320S subunits to bind norleucine. With glutamate at pH 8.8, an h value of 3.6 was obtained for the 1:5 hybrid, in contrast with an h value of 5.2 for the C320S homohexamer. The "foreign" subunit evidently impedes inter-subunit communication to some extent.

Entities:  

Mesh:

Substances:

Year:  2001        PMID: 11736656      PMCID: PMC1222269          DOI: 10.1042/0264-6021:3600651

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


  26 in total

1.  Construction, separation and properties of hybrid hexamers of glutamate dehydrogenase in which five of the six subunits are contributed by the catalytically inert D165S.

Authors:  B M Hayden; P C Engel
Journal:  Eur J Biochem       Date:  2001-03

2.  Construction and investigation of co-operativity in hybrids of norleucine- and glutamate-active subunits of clostridial glutamate dehydrogenase.

Authors:  A Goyal; S Aghajanian; B M Hayden; X G Wang; P C Engel
Journal:  Biochem Soc Trans       Date:  1998-02       Impact factor: 5.407

3.  Positive cooperativity with Hill coefficients of up to 6 in the glutamate concentration dependence of steady-state reaction rates measured with clostridial glutamate dehydrogenase and the mutant A163G at high pH.

Authors:  X G Wang; P C Engel
Journal:  Biochemistry       Date:  1995-09-12       Impact factor: 3.162

4.  Alteration of the quaternary structure of glutamate dehydrogenase from Clostridium symbiosum by a single mutation distant from the subunit interfaces.

Authors:  J L Dean; H Cölfen; S E Harding; D W Rice; P C Engel
Journal:  Eur Biophys J       Date:  1997       Impact factor: 1.733

5.  Kinetic studies of glutamate dehydrogenase with glutamate and norvaline as substrates. Coenzyme activation and negative homotropic interactions in allosteric enzymes.

Authors:  P C Engel; K Dalziel
Journal:  Biochem J       Date:  1969-12       Impact factor: 3.857

6.  Multivalent regulation of glutamic dehydrogenases from fungi. Effects of adenylates, guanylates, and acyl coenzyme A derivatives.

Authors:  H B LéJohn; R M Stevenson; R Meuser
Journal:  J Biol Chem       Date:  1970-11-10       Impact factor: 5.157

7.  Conversion of a glutamate dehydrogenase into methionine/norleucine dehydrogenase by site-directed mutagenesis.

Authors:  X G Wang; K L Britton; T J Stillman; D W Rice; P C Engel
Journal:  Eur J Biochem       Date:  2001-11

8.  Identification of the reactive cysteine in clostridial glutamate dehydrogenase by site-directed mutagenesis and proof that this residue is not strictly essential.

Authors:  X G Wang; P C Engel
Journal:  Protein Eng       Date:  1994-08

9.  Site and significance of chemically modifiable cysteine residues in glutamate dehydrogenase of Clostridium symbiosum and the use of protection studies to measure coenzyme binding.

Authors:  S E Syed; D P Hornby; P E Brown; J E Fitton; P C Engel
Journal:  Biochem J       Date:  1994-02-15       Impact factor: 3.857

10.  The catalytic role of aspartate in the active site of glutamate dehydrogenase.

Authors:  J L Dean; X G Wang; J K Teller; M L Waugh; K L Britton; P J Baker; T J Stillman; S R Martin; D W Rice; P C Engel
Journal:  Biochem J       Date:  1994-07-01       Impact factor: 3.857

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.