Document Detail


Changes in the carboxyl terminus of the beta subunit of human propionyl-CoA carboxylase affect the oligomer assembly and catalysis: expression and characterization of seven patient-derived mutant forms of PCC in Escherichia coli.
MedLine Citation:
PMID:  11136555     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Propionyl-CoA carboxylase (PCC) catalyzes the biotin-dependent carboxylation of propionyl-CoA to d-methylmalonyl-CoA in the mitochondrial matrix. Human PCC is a dodecamer composed of pairs of nonidentical alpha and beta subunits encoded by PCCA and PCCB genes, respectively. Deficiency of PCC results in propionic acidemia (PA), a metabolic disorder characterized by severe metabolic ketoacidosis, vomiting, lethargy, and hypotonia. To date, almost 60 mutations have been reported in both genes. Exon 15 of the beta subunit is one of the two sites where a number of mutations have been identified in PA patients. In the primary betaPCC sequence, these mutations lead to three substitutions (R512C, L519P, and N536D), three truncations (R499X, R514X, and W531X), and one insertion (A51_R514insP). We expressed these mutant proteins in Escherichia coli in which the GroESL complex was overexpressed. The only mutation that does not impact the stability of mutant betaPCC in bacteria is W531X. The remaining mutations lead to either complete (L519P, N536D) or partial (R499X, R512C, A513_R514insP, and R514X) degradation of the mutant subunits. Size-exclusion chromatography revealed that R512C and W531X do not affect the assembly of alphaPCC and betaPCC to active oligomers. Specific activities for these mutant proteins, however, were only 3.9 and 10% of the wild type, respectively. Taken together, the carboxyl-terminal portion of 40 amino acid residues of the beta subunit affects the stability and the assembly of the alpha and beta subunits as well as the carboxylation of propionyl-CoA.
Authors:
M Chloupková; K Ravn; M Schwartz; J P Kraus
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Publication Detail:
Type:  Journal Article; Research Support, U.S. Gov't, P.H.S.    
Journal Detail:
Title:  Molecular genetics and metabolism     Volume:  71     ISSN:  1096-7192     ISO Abbreviation:  Mol. Genet. Metab.     Publication Date:  2000 Dec 
Date Detail:
Created Date:  2001-01-23     Completed Date:  2001-01-26     Revised Date:  2007-11-14    
Medline Journal Info:
Nlm Unique ID:  9805456     Medline TA:  Mol Genet Metab     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  623-32     Citation Subset:  IM    
Copyright Information:
Copyright 2000 Academic Press.
Affiliation:
Department of Pediatrics, University of Colorado School of Medicine, Denver, Colorado 80262, USA.
Data Bank Information
Bank Name/Acc. No.:
GENBANK/X73424
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MeSH Terms
Descriptor/Qualifier:
Amino Acid Sequence
Base Sequence
Blotting, Western
Carboxy-Lyases / chemistry,  genetics*,  metabolism*
Catalysis
Chromatography, Gel
Enzyme Stability
Escherichia coli / genetics*
Exons / genetics
Fibroblasts
Genotype
Humans
Metabolism, Inborn Errors / enzymology*,  genetics*
Methylmalonyl-CoA Decarboxylase
Mitochondria / enzymology
Molecular Sequence Data
Mutation / genetics*
Oligodeoxyribonucleotides
Phenotype
Propionic Acids / blood,  metabolism
Protein Structure, Quaternary
Protein Subunits
Recombinant Proteins / chemistry,  metabolism
Grant Support
ID/Acronym/Agency:
P01HD08315/HD/NICHD NIH HHS
Chemical
Reg. No./Substance:
0/Oligodeoxyribonucleotides; 0/Propionic Acids; 0/Protein Subunits; 0/Recombinant Proteins; 79-09-4/propionic acid; EC 4.1.1.-/Carboxy-Lyases; EC 4.1.1.41/Methylmalonyl-CoA Decarboxylase

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


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