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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
2
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pubmed:dateCreated |
1976-5-20
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pubmed:abstractText |
1. The nature of the acetyl-CoA hydrolase (EC 3.1.2.1) reaction in rat and sheep liver homogenates was investigated. 2. The activity determined in an incubated system was 5.10 and 3.28nmol/min per mg of protein for rat and sheep liver homogenate respectively. This activity was not affected by the addition of l-carnitine, but was decreased by the addition of d-carnitine. 3. No acetyl-CoA hydrolase activity could be detected in rat or sheep liver homogenates first treated with Sephadex G-25. This treatment decreased the carnitine concentrations of the homogenates to about one-twentieth. Subsequent addition of l-carnitine, but not d-carnitine, restored the apparent acetyl-CoA hydrolase activity. 4. Sephadex treatment did not affect acetyl-carnitine hydrolase activity of the homogenates, which was 5.8 and 8.1nmol/min per mg of protein respectively for rat and sheep liver. 5. Direct spectrophotometric assay of acetyl-CoA hydrolase, based on the reaction of CoA released with 5,5'-dithiobis-(2-nitrobenzoic acid), clearly demonstrated that after Sephadex treatment no activity could be measured. 6. Carnitine acetyltransferase (EC 2.3.1.7) activity measured in the same assay system in response to added l-carnitine was very low in normal rat liver homogenates, owing to the apparent high acetyl-CoA hydrolase activity, but was increased markedly after Sephadex treatment. The V(max.) for this enzyme in rat liver homogenates was increased from 3.4 to 14.8nmol/min per mg of protein whereas the K(m) for l-carnitine was decreased from 936 to 32mum after Sephadex treatment. 7. Acetyl-CoA hydrolase activity could be demonstrated in disrupted rat liver mitochondria but not in separated outer or inner mitochondrial membrane fractions. Activity could be demonstrated after recombination of outer and inner mitochondrial membrane fractions. The outer mitochondrial membrane fraction showed acetylcarnitine hydrolase activity and the inner mitochondrial membrane fraction showed carnitine acetyltransferase activity. 8. The results presented here demonstrate that acetyl-CoA hydrolase activity in rat and sheep liver is an artifact and the activity is due to the combined activity of carnitine acetyltransferase and acetylcarnitine hydrolase.
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/1220678-12999747,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1220678-13785321,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1220678-13963148,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1220678-14166729,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1220678-14174004,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1220678-14299645,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1220678-4059,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1220678-4307302,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1220678-4441381,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1220678-4643343,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1220678-4681845,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1220678-4850896,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1220678-5058225,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1220678-5059948,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1220678-5073738,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1220678-5360406,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1220678-5485754,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1220678-5704822,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1220678-5763788,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1220678-6069132
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0264-6021
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
152
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
167-72
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pubmed:dateRevised |
2010-9-7
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pubmed:meshHeading |
pubmed-meshheading:1220678-Acetyl Coenzyme A,
pubmed-meshheading:1220678-Acetyltransferases,
pubmed-meshheading:1220678-Animals,
pubmed-meshheading:1220678-Carnitine,
pubmed-meshheading:1220678-Carnitine O-Acetyltransferase,
pubmed-meshheading:1220678-Coenzyme A,
pubmed-meshheading:1220678-Female,
pubmed-meshheading:1220678-Kinetics,
pubmed-meshheading:1220678-Liver,
pubmed-meshheading:1220678-Membranes,
pubmed-meshheading:1220678-Mitochondria, Liver,
pubmed-meshheading:1220678-Rats,
pubmed-meshheading:1220678-Sheep,
pubmed-meshheading:1220678-Stereoisomerism,
pubmed-meshheading:1220678-Thiolester Hydrolases
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pubmed:year |
1975
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pubmed:articleTitle |
Acetyl-coenzyme A hydrolase, an artifact? The conversion of acetyl-coenzyme A into acetate by the combined action of carnitine acetyltransferase and acetylcarnitine hydrolase.
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pubmed:publicationType |
Journal Article
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