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PMID: 11171137 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't

Molecular biology of cytosolic acetyl-CoA generation.

Biochemical Society transactions ·Vol. 28 ·No. 6 ·2000-12-00 ·Pages 593-5

Fatland B, Anderson M, Nikolau BJ, Wurtele ES

Abstract

ATP citrate lyase (ACL) catalyses the ATP-dependent reaction between citrate and CoA to form oxaloacetate and acetyl-CoA. Our molecular characterizations of the cDNAs and genes coding for the Arabidopsis ACL indicate that the plant enzyme is heteromeric, consisting of two dissimilar subunits. The A subunit is homologous to the N-terminal third of the animal ACL, and the B subunit is homologous to C-terminal two-thirds of the animal ACL. Using both ACL-A- and ACL-B-specific antibodies and activity assays we have shown that ACL is located in the cytosol, and is not detectable in the plastids, mitochondria or peroxisomes. During seed development, ACL-A and ACL-B mRNA accumulation is co-ordinated with the accumulation of the cytosolic homomeric acetyl-CoA carboxylase mRNA. Antisense Arabidopsis plants reduced in ATP citrate lyase activity show a complex phenotype, with miniaturized organs, small cell size, aberrant plastid morphology and reduced cuticular wax. Our results indicate that ACL generates the cytosolic pool of acetyl-CoA, which is the substrate required for the biosynthesis of a variety of phytochemicals, including cuticular waxes and flavonoids.

MeSH Terms
ATP Citrate (pro-S)-Lyase/genetics,metabolism Acetyl Coenzyme A/biosynthesis,metabolism Animals Arabidopsis/enzymology,genetics,growth & development Cytosol/enzymology Molecular Biology/methods Plants, Genetically Modified/enzymology Protein Subunits Seeds/enzymology
Chemicals
Protein Subunits Acetyl Coenzyme A ATP Citrate (pro-S)-Lyase
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Fatland B
Department of Botany, Iowa State University, Ames, IA 50011, USA.
Anderson M
Nikolau B J
Wurtele E S
Article Info
Journal
Biochemical Society transactions
Abbr.
Biochem Soc Trans
ISSN
0300-5127
Published
2000-12-00
Pages
593-5
Language
English
Region
England
NLM ID
7506897
Subset
IM
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