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过氧化物酶体脂肪酸β氧化 被引量:15

Recent Advances in Peroxisomal Fatty Acid β-Oxidation
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摘要 除线粒体外,过氧化物酶体也是真核细胞脂肪酸β氧化分解的重要部位.过氧化物酶体β氧化过程包括氧化、加水、脱氢和硫解4步反应,主要参与极长链、支链脂肪酸等的分解.近年关于过氧化物酶体β氧化的研究活跃,在代谢途径及功能等方面有了新的认识,尤其在对相关代谢酶的研究中取得了较大进展.本文就过氧化物酶体β氧化相关进展作一综述. Besides mitochondria, peroxisomes are subcellular organelles that are capable of conductmg β- oxidation of fatty acids in eukaryocytes. Peroxisomal fatty acid β-oxidation consists of four sequential enzymatic steps (oxidation, hydratation, dehydrogenation, and thiolytic cleavage), and results in the degradation of long-chain fatty acids or 2-methyl-branched fatty acids. In recent years, studies on peroxisomal fatty acid β- oxidation have become an active research focus, and substantial progresses have been made, especially for the metabolic enzymes. This article will review the recent advances in aspects of the functional characteristics, metabolic enzymes, regulation, and deficiencies of peroxisomal fatty acid β-oxidation.
出处 《中国生物化学与分子生物学报》 CAS CSCD 北大核心 2009年第1期12-16,共5页 Chinese Journal of Biochemistry and Molecular Biology
基金 国家自然科学基金资助项目(No.30371566)~~
关键词 过氧化物酶体 脂肪酸 β氧化 代谢酶 peroxisome fatty acids β-oxidation metabolic enzyme
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  • 1Lazarow P B, De Duve C. A fatty acyl-CoA oxidizing system in rat liver peroxisomes; enhancement by clofibrate, a hypolipidemic drug [J]. Proc Natl Acad Sci USA, 1976, 73(6) :2043-2046 被引量:1
  • 2Latruffe N, Vamecq J, Cherkaoui Malki M. Genetic-dependency of peroxisomal cell functions-emerging aspects [ J ]. J Cell Mol Med, 2003, 7(3) :238-248 被引量:1
  • 3Ferdinandusse S, Meissner T, Wanders R J, et al. Identification of the peroxisomal beta-oxidation enzymes involved in the degradation of leukotrienes[J]. Biochcm Biophys Res Commun, 2002, 293 ( 1 ) : 269-273 被引量:1
  • 4Ferdinandusse S, Denis S, Mooijer P A, et al. Identification of the peroxisomal beta-oxidation enzymes involved in the biosynthesis of docosahexaenoic acid[J]. J Lipid Res, 2001, 42(12):1987-1995 被引量:1
  • 5Hovik R, Osmundsen H. Peroxisomal beta-oxidation of long-chain fatty acids possessing different extents of unsaturation[ J]. Biochem J, 1987, 247(3) :531-535 被引量:1
  • 6Visser W F, van Roermund C W, Ijlst L, et al. Metabolite transport across the peroxisomal membrane [ J ]. Biochem J, 2007, 401 ( 2 ) : 365-375 被引量:1
  • 7Hashimoto T. Peroxisomal beta-oxidation enzymes[J]. Cell Biochem Biophys, 2000, 32 Spring:63-72 被引量:1
  • 8Mihalik S J, Steinberg S J, Pei Z, et al. Participation of two members of the very long-chain acyl-CoA synthetase family in bile acid synthesis and recycling [J]. J Biol Chem, 2002, 277 ( 27 ) : 24771-24779 被引量:1
  • 9Watkins P A, Howard A E, Gould S J, et al. Phytanic acid activation in rat liver peroxisomes is catalyzed by long-chain acyl-CoA synthetase[J]. J Lipid Res, 1996, 37(11) :2288-2295 被引量:1
  • 10Watkins P A. Very-long-chain acyl-CoA synthetases [ J ]. J Biol Chem, 2008, 283(4) : 1773-1777 被引量:1

二级参考文献23

  • 1石如玲,赵朝贤,朱海暴,杨原,王素玲,姜玲玲.大鼠肝脏D-双功能蛋白活性增加与胆汁酸合成的关系[J].中国医学科学院学报,2005,27(3):321-324. 被引量:4
  • 2Jiang LL, Kobayashi A, Matsuura H, et al. Purification and properties of human D-3-Hydroxyacyl-CoA dehydratase:medium-chain enoyl-CoA hydratase is D-3-HydroxyacylCoA dehydratase. J Biochem, 1996, 120(3):624-632 被引量:1
  • 3Jiang LL, Miyazawa S, Hashimoto T. Purification and properties of rat D-3-hydroxyacyl-CoA dehydratase: D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein. J Biochem (Tokyo), 1996, 120(3):633-641 被引量:1
  • 4Jiang LL, Kurosawa T, Sato M. Physiological role of D-3hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein. J Biochem (Tokyo), 1997, 121(3):506-513 被引量:1
  • 5Kurosawa T, Sato M, Jiang LL, et al. Stereospecific formation of (24R, 25R)-3 alpha, 7 alpha, 12 alpha, 24-tetrahydroxy-5 beta-cholestan-26-oic acid catalyzed with a peroxisomal bifunctional D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase. Biol Pharm Bull, 1997,20(3):295-297 被引量:1
  • 6Suzuki Y, Jiang LL, Souri M, et al. D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiency: a newly identified peroxisomal disorder.Am J Hum Genet, 1997, 61(5):1153-1162 被引量:1
  • 7Baes M, Huyghe S, Carmeliet P, et al. Inactivation of the peroxisomal multifunctional protein-2 in mice impedes the degradation of not only 2-methyl-branched fatty acids and bile acid intermediates but also of very long chain fatty acids. J Biol Chem, 2000, 275(21):16329-16336 被引量:1
  • 8Kajiura K, Ohkusa T, Okayasu I. Relationship between fecal bile acids and the occurrence of colorectal neoplasia in experimental murine ulcerative colitis. Digestion, 1998,59(1):69-72 被引量:1
  • 9Kobayashi A, Jiang LL, Hashimoto T. Two mitochondrial 3-hydroxyacyl-CoA dehydrogenases in bovine liver. J Biochem (Tokyo), 1996, 119(4):775-782 被引量:1
  • 10Palosaari PM, Hiltunen JK. Peroxisomal bifunctional protein from rat liver is a trifunctional enzyme possessing 2-enoylCoA hydratase, 3-hydroxyacyl-CoA dehydrogenase, and delta 3, delta 2-enoyl-CoA isomerase activities. J Biol Chem, 1990,265 (5):2446-2449 被引量:1

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