Literature DB >> 2572585

Formation of malonyl coenzyme A in rat heart. Identification and purification of an isozyme of A carboxylase from rat heart.

K G Thampy1.   

Abstract

Acetyl-CoA carboxylase is thought to be absent in the heart since the latter is highly catabolic and nonlipogenic. It has been suggested that the high level of malonyl-CoA that is found in the heart is derived from mitochondrial propionyl-CoA carboxylase, which also uses acetyl-CoA. In the present study, acetyl-CoA carboxylase was identified and purified from homogenates of rat heart. The isolated enzyme had little activity in the absence of citrate (specific activity, less than 0.1 units/mg); however, citrate stimulated its activity (specific activity, 1.8 units/mg in the presence of 10 mM citrate). Avidin inhibited greater than 95% of activity, and addition of biotin reversed this inhibition. Further, malonyl-CoA (1 mM) and palmitoyl-CoA (100 microM) inhibited greater than 90% of carboxylase activity. Similar to acetyl-CoA carboxylase of lipogenic tissues, the heart enzyme could be activated greater than 6-fold by preincubation with liver (acetyl-CoA carboxylase)-phosphatase 2. The activation was accompanied by a decrease in the K0.5 for citrate to 0.68 mM. These observations suggest that the activity in preparations from heart is due to authentic acetyl-CoA carboxylase. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis of the preparation from heart showed the presence of one major protein band (Mr 280,000) and a minor band (Mr 265,000) while that from liver gave a major protein band (Mr 265,000). A Western blot probed with avidin-peroxidase suggested that both the 280- and 265-kDa species contained biotin. Antibodies to liver acetyl-CoA carboxylase, which inhibited greater than 95% of liver carboxylase activity, inhibited only 35% of heart enzyme activity. In an immunoblot (using antibodies to liver enzyme) the 265-kDa species, and not the major 280-kDa species, in the heart preparation was specifically stained. These observations suggest the presence of two isoenzymes of acetyl-CoA carboxylase that are immunologically distinct, the 265-kDa species being predominant in the liver and the 280-kDa species being predominant in the heart.

Entities:  

Mesh:

Substances:

Year:  1989        PMID: 2572585

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  30 in total

1.  Induced polymerization of mammalian acetyl-CoA carboxylase by MIG12 provides a tertiary level of regulation of fatty acid synthesis.

Authors:  Chai-Wan Kim; Young-Ah Moon; Sahng Wook Park; Dong Cheng; Hyock Joo Kwon; Jay D Horton
Journal:  Proc Natl Acad Sci U S A       Date:  2010-05-10       Impact factor: 11.205

2.  Cellular expression of a monocarboxylate transporter (MCT1) in the mammary gland and sebaceous gland of mice.

Authors:  Kumiko Takebe; Junko Nio-Kobayashi; Hiromi Takahashi-Iwanaga; Takaji Yajima; Toshihiko Iwanaga
Journal:  Histochem Cell Biol       Date:  2008-12-02       Impact factor: 4.304

3.  Alterations in nutritional status regulate acetyl-CoA carboxylase expression in avian liver by a transcriptional mechanism.

Authors:  F B Hillgartner; T Charron; K A Chesnut
Journal:  Biochem J       Date:  1996-10-01       Impact factor: 3.857

4.  Cloning of human acetyl-CoA carboxylase-beta and its unique features.

Authors:  J Ha; J K Lee; K S Kim; L A Witters; K H Kim
Journal:  Proc Natl Acad Sci U S A       Date:  1996-10-15       Impact factor: 11.205

5.  Multiple-site phosphorylation of the 280 kDa isoform of acetyl-CoA carboxylase in rat cardiac myocytes: evidence that cAMP-dependent protein kinase mediates effects of beta-adrenergic stimulation.

Authors:  A N Boone; B Rodrigues; R W Brownsey
Journal:  Biochem J       Date:  1999-07-15       Impact factor: 3.857

6.  Biotin carboxylases in mitochondria and the cytosol from skeletal and cardiac muscle as detected by avidin binding.

Authors:  S Kirkeby; D Moe; T C Bøg-Hansen; C J van Noorden
Journal:  Histochemistry       Date:  1993-12

7.  Analytical and micropreparative peptide mapping by high performance liquid chromatography/electrospray mass spectrometry of proteins purified by gel electrophoresis.

Authors:  D Hess; T C Covey; R Winz; R W Brownsey; R Aebersold
Journal:  Protein Sci       Date:  1993-08       Impact factor: 6.725

Review 8.  Energy metabolism in the normal and failing heart: potential for therapeutic interventions.

Authors:  William C Stanley; Margaret P Chandler
Journal:  Heart Fail Rev       Date:  2002-04       Impact factor: 4.214

9.  Mutant mice lacking acetyl-CoA carboxylase 1 are embryonically lethal.

Authors:  Lutfi Abu-Elheiga; Martin M Matzuk; Parichher Kordari; WonKeun Oh; Tattym Shaikenov; Ziwei Gu; Salih J Wakil
Journal:  Proc Natl Acad Sci U S A       Date:  2005-08-15       Impact factor: 11.205

10.  Malonyl-CoA metabolism in cardiac myocytes and its relevance to the control of fatty acid oxidation.

Authors:  M M Awan; E D Saggerson
Journal:  Biochem J       Date:  1993-10-01       Impact factor: 3.857

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.