نتایج جستجو برای: malonyl

تعداد نتایج: 1296  

Journal: :Diabetes 2006
Gautam K Bandyopadhyay Joseph G Yu Jachelle Ofrecio Jerrold M Olefsky

Increased accumulation of fatty acids and their derivatives can impair insulin-stimulated glucose disposal by skeletal muscle. To characterize the nature of the defects in lipid metabolism and to evaluate the effects of thiazolidinedione treatment, we analyzed the levels of triacylglycerol, long-chain fatty acyl-coA, malonyl-CoA, fatty acid oxidation, AMP-activated protein kinase (AMPK), acetyl...

Journal: :Molecular and cellular biology 2007
Naomoto Harada Zenjun Oda Yoshikazu Hara Koji Fujinami Mayumi Okawa Katsuya Ohbuchi Mari Yonemoto Yuika Ikeda Kenji Ohwaki Katsumi Aragane Yoshitaka Tamai Jun Kusunoki

Acetyl coenzyme A (acetyl-CoA) carboxylase (ACC) catalyzes carboxylation of acetyl-CoA to form malonyl-CoA. In mammals, two isozymes exist with distinct physiological roles: cytosolic ACC1 participates in de novo lipogenesis (DNL), and mitochondrial ACC2 is involved in negative regulation of mitochondrial beta-oxidation. Since systemic ACC1 null mice were embryonic lethal, to clarify the physio...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2011
Su Gao Guangjing Zhu Xuefei Gao Donghai Wu Patricia Carrasco Núria Casals Fausto G Hegardt Timothy H Moran Gary D Lopaschuk

Brain-specific carnitine palmitoyltransferase-1 (CPT-1c) is implicated in CNS control of food intake. In this article, we explore the role of hypothalamic CPT-1c in leptin's anorexigenic actions. We first show that adenoviral overexpression of CPT-1c in hypothalamic arcuate nucleus of rats increases food intake and concomitantly up-regulates orexigenic neuropeptide Y (NPY) and Bsx (a transcript...

Journal: :The Journal of antibiotics 2003
Hrvoje Petkovic Rachel E Lill Rose M Sheridan Barrie Wilkinson Ellen L McCormick Hamish A I McArthur James Staunton Peter F Leadlay Steven G Kendrew

The acyltransferase (AT) domain in module 4 of the erythromycin polyketide synthase (PKS) was substituted with an AT domain from the rapamycin PKS module 2 in order to alter the substrate specificity from methylmalonyl-CoA to malonyl-CoA. The resulting strain produced 6-desmethyl erythromycin D as the predominant product. This AT domain swap completes the library of malonyl-CoA AT swaps on the ...

Journal: :The Biochemical journal 2004
Gha Young Lee Nam Hee Kim Zheng-Shan Zhao Bong Soo Cha Yu Sam Kim

MCD (malonyl-CoA decarboxylase), which catalyses decarboxylation of malonyl-CoA, is known to play an important role in the regulation of malonyl-CoA concentration. Recently, it has been observed that the expression of MCD is significantly decreased in the hearts of the PPARalpha (peroxisome-proliferator-activated receptor alpha) (-/-) mice, where the rate of fatty-acid oxidation is decreased by...

Journal: :The American journal of physiology 1996
W W Winder D G Hardie

Malonyl-CoA, an inhibitor of fatty acid oxidation in skeletal muscle mitochondria, decreases in rat skeletal muscle during exercise or in response to electrical stimulation. Regulation of rat skeletal muscle acetyl-CoA carboxylase (ACC), the enzyme that synthesizes malonyl-CoA, was studied in vitro and in vivo. Avidin-Sepharose affinity-purified ACC from hindlimb skeletal muscle was phosphoryla...

Journal: :The Journal of biological chemistry 1985
Y S Kim S K Bang

Malonyl coenzyme A synthetase (EC 6.2.1.14) was induced in Pseudomonas fluorescens grown on malonate as a sole carbon source. This enzyme was purified, for the first time, over 30-fold by the combination of ammonium sulfate precipitation, Sephadex G-150 gel filtration, DEAE-Sephacel ion exchange chromatography, and hydroxylapatite chromatography. The purified enzyme, which had a specific activi...

Journal: :The Biochemical journal 1996
L Drynan P A Quant V A Zammit

The relationships between the increase in blood ketone-body concentrations and several parameters that can potentially influence the rate of hepatic fatty acid oxidation were studied during progressive starvation (up to 24 h) in the rat in order to discover whether the sensitivity of mitochondrial overt carnitine palmitoyltransferase (CPT I) to malonyl-CoA plays an important part in determining...

Journal: :Biochemical Society transactions 1990
G A Cook L J Weakley

I t is generally accepted that the mitochondria1 carnitine palmitoyltransferases play an important role in the regulation of hepatic fatty acid oxidation [ I ] . These two enzymes express their activities on either side of the mitochondrial inner membrane that acts as a barrier to the transfer of fatty acids into the mitochondrial matrix. The enzyme that lies outsidc this barrier is located on ...

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