Document Detail


Substrate specificity determinants of the methanogen homoaconitase enzyme: structure and function of the small subunit.
MedLine Citation:
PMID:  20170198     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The aconitase family of hydro-lyase enzymes includes three classes of proteins that catalyze the isomerization of alpha-hydroxy acids to beta-hydroxy acids. Besides aconitase, isopropylmalate isomerase (IPMI) proteins specifically catalyze the isomerization of alpha,beta-dicarboxylates with hydrophobic gamma-chain groups, and homoaconitase (HACN) proteins catalyze the isomerization of tricarboxylates with variable chain length gamma-carboxylate groups. These enzymes' stereospecific hydro-lyase activities make them attractive catalysts to produce diastereomers from unsaturated precursors. However, sequence similarity and convergent evolution among these proteins lead to widespread misannotation and uncertainty about gene function. To find the substrate specificity determinants of homologous IPMI and HACN proteins from Methanocaldococcus jannaschii, the small-subunit HACN protein (MJ1271) was crystallized for X-ray diffraction. The structural model showed characteristic residues in a flexible loop region between alpha2 and alpha3 that distinguish HACN from IPMI and aconitase proteins. Site-directed mutagenesis of MJ1271 produced loop-region variant proteins that were reconstituted with wild-type MJ1003 large-subunit protein. The heteromers formed promiscuous hydro-lyases with reduced activity but broader substrate specificity. Both R26K and R26V variants formed relatively efficient IPMI enzymes, while the T27A variant had uniformly lower specificity constants for both IPMI and HACN substrates. The R26V T27Y variant resembles the MJ1277 IPMI small subunit in its flexible loop sequence but demonstrated the broad substrate specificity of the R26V variant. These mutations may reverse the evolution of HACN activity from an ancestral IPMI gene, demonstrating the evolutionary potential for promiscuity in hydro-lyase enzymes. Understanding these specificity determinants enables the functional reannotation of paralogous HACN and IPMI genes in numerous genome sequences. These structural and kinetic results will help to engineer new stereospecific hydro-lyase enzymes for chemoenzymatic syntheses.
Authors:
Jeyaraman Jeyakanthan; Randy M Drevland; Dasara Raju Gayathri; Devadasan Velmurugan; Akeo Shinkai; Seiki Kuramitsu; Shigeyuki Yokoyama; David E Graham
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.    
Journal Detail:
Title:  Biochemistry     Volume:  49     ISSN:  1520-4995     ISO Abbreviation:  Biochemistry     Publication Date:  2010 Mar 
Date Detail:
Created Date:  2010-03-23     Completed Date:  2010-04-23     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  0370623     Medline TA:  Biochemistry     Country:  United States    
Other Details:
Languages:  eng     Pagination:  2687-96     Citation Subset:  IM    
Affiliation:
Life Science Group, National Synchrotron Radiation Research Center, 101 Hsin-Ann Road, Hsinchu Science Park, Hsinch 30076, Taiwan.
Data Bank Information
Bank Name/Acc. No.:
PDB/2PKP
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MeSH Terms
Descriptor/Qualifier:
Aconitate Hydratase / chemistry
Amino Acid Substitution
Archaeal Proteins / chemistry
Base Sequence
Binding Sites / genetics*
Catalysis
Euryarchaeota / enzymology,  metabolism
Evolution, Molecular
Hydro-Lyases / chemistry*,  genetics
Isomerases / chemistry
Kinetics
Models, Molecular
Molecular Sequence Data
Mutagenesis, Site-Directed / methods*
Protein Conformation
Protein Subunits
Sequence Alignment
Structure-Activity Relationship
Substrate Specificity / genetics*
Chemical
Reg. No./Substance:
0/Archaeal Proteins; 0/Protein Subunits; EC 4.2.1.-/Hydro-Lyases; EC 4.2.1.3/Aconitate Hydratase; EC 4.2.1.33/isopropylmalate isomerase; EC 4.2.1.36/homoaconitate hydratase; EC 5.-/Isomerases

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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