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Lipid Biosynthesis in Peroxisomes a

dc.contributor.authorHajra, Amiya K.en_US
dc.contributor.authorDas, Arun K.en_US
dc.date.accessioned2010-06-01T21:36:55Z
dc.date.available2010-06-01T21:36:55Z
dc.date.issued1996-12en_US
dc.identifier.citationHAJRA, AMIYA K.; DAS, ARUN K. (1996). "Lipid Biosynthesis in Peroxisomes a ." Annals of the New York Academy of Sciences 804(1 Peroxisomes: Biology and Role in Toxicology and Disease ): 129-141. <http://hdl.handle.net/2027.42/74665>en_US
dc.identifier.issn0077-8923en_US
dc.identifier.issn1749-6632en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/74665
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=8993541&dopt=citationen_US
dc.format.extent707805 bytes
dc.format.extent3109 bytes
dc.format.mimetypeapplication/pdf
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dc.publisherBlackwell Publishing Ltden_US
dc.rights1996 The New York Academy of Sciencesen_US
dc.titleLipid Biosynthesis in Peroxisomes aen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelScience (General)en_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumMental Health Research Institute and Department of Biological Chemistry University of Michigan Ann Arbor, Michigan 48109en_US
dc.identifier.pmid8993541en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/74665/1/j.1749-6632.1996.tb18613.x.pdf
dc.identifier.doi10.1111/j.1749-6632.1996.tb18613.xen_US
dc.identifier.sourceAnnals of the New York Academy of Sciencesen_US
dc.identifier.citedreferenceJones, C. L. & A. K. Hajra. 1977. The subcellular distribution of acyl CoA: Dihydroxy-acetone phosphate acyl transferase in guinea pig liver. Biochem. Biophys. Res. Commun. 76: 1138 – 1143.en_US
dc.identifier.citedreferencede Duve, C. & P. Baudhuin. 1966. Peroxisomes (microbodies and related particles). Physiol. Rev. 46: 323 – 357.en_US
dc.identifier.citedreferenceHajra, A. K. & J. E. Bishop. 1982. Glycerolipid biosynthesis in peroxisomes via the acyl dihydroxyacetone phosphate pathway. Ann. N.Y. Acad. Sci. 386: 170 – 182.en_US
dc.identifier.citedreferenceKase, B. F., I. BjÖrkhem & J. I. Pedersen. 1983. Formation of cholic acid from 3 alpha, 7 alpha, 12 alpha-trihydroxy-5 beta-cholestanoic acid by rat liver peroxisomes. J. Lipid Res. 24: 1560 – 1567.en_US
dc.identifier.citedreferenceKrisans, S. K. 1992. The role of peroxisomes in cholesterol metabolism. Am. J. Respir. Cell. Mol. Biol. 7: 358 – 364.en_US
dc.identifier.citedreferenceHajra, A. K. & B. W. Agranoff. 1967. Acyl dihydroxyacetone phosphate: A rapidly labeled lipid in guinea pig liver mitochondria. J. Biol. Chem. 242: 1074 – 1075.en_US
dc.identifier.citedreferenceHajra, A. K. 1968. Biosynthesis of acyl dihydroxyacetone phosphate in guinea pig liver mitochondria. J. Biol. Chem. 243: 3458 – 3465.en_US
dc.identifier.citedreferenceJones, C. L. & A. K. Hajra. 1980. Properties of guinea pig liver peroxisomal dihydroxyacetone phosphate acyltransferase. J. Biol. Chem. 255: 8289 – 8295.en_US
dc.identifier.citedreferenceHajra, A. K. 1983. Biosynthesis of O -Alkylglycerol Ether Lipids. In Ether Lipids. H. Mangold & F. Paltauf, Eds.: 85 – 106. Academic Press. New York.en_US
dc.identifier.citedreferenceLaBelle, E. F., Jr. & A. K. Hajra. 1972. Enzymatic reduction of alkyl and acyl derivatives of dihydroxyacetone phosphate by reduced pyridine nucleotides. J. Biol. Chem. 247: 5825 – 5834.en_US
dc.identifier.citedreferenceHajra, A. K. 1970. Acyl dihydroxyacetone phosphate: Precursor of alkyl ethers. Biochem. Biophys. Res. Commun. 39: 1037 – 1044.en_US
dc.identifier.citedreferenceDatta, S. C., M. K. Ghosh & A. K. Hajra. 1990. Purification and properties of acyl/alkyl dihydroxyacetone-phosphate reductase from guinea pig liver peroxisomes. J. Biol. Chem. 265: 8268 – 8274.en_US
dc.identifier.citedreferenceKennedy, E. P. 1962. The metabolism and function of complex lipids. Harvey Lec. 57: 143 – 171.en_US
dc.identifier.citedreferenceHajra, A. K. & C. L. Burke. 1978. Biosynthesis of phosphatidic acid in rat brain via acyl dihydroxyacetone phosphate. J. Neurochem. 31: 125 – 134.en_US
dc.identifier.citedreferenceHajra, A. K., C. L. Burke & C. L. Jones. 1979. Subcellular localization of acyl coenzyme A: Dihydroxyacetone phosphate acyltransferase in rat liver peroxisomes (microbodies). J. Biol. Chem. 254: 10896 – 10900.en_US
dc.identifier.citedreferenceHajra, A. K. & D. Wu. 1985. Preparative isolation of peroxisomes from liver and kidney using metrizamide density gradient centrifugation in a vertical rotor. Anal. Biochem. 148: 233 – 244.en_US
dc.identifier.citedreferenceGhosh, M. K. & A. K. Hajra. 1986. A rapid method for the isolation of peroxisomes from rat liver. Anal. Biochem. 159: 169 – 174.en_US
dc.identifier.citedreferenceGhosh, A. K. & A. K. Hajra. 1986. Subcellular distribution and properties of acyl/alkyl dihydroxyacetone phosphate reductase in rodent livers. Arch. Biochem. Biophys. 245: 523 – 530.en_US
dc.identifier.citedreferencevan den Bosch H., R. Schutgens, R. J. Wanders & J. M. Tager. 1992. Biochemistry of peroxisomes. Annu. Rev. Biochem. 61: 157 – 197.en_US
dc.identifier.citedreferenceBishop, J. E. & A. K. Hajra. 1981. Mechanism and specificity of formation of long chain alcohols by developing rat brain. J. Biol. Chem. 256: 9542 – 9550.en_US
dc.identifier.citedreferenceBurdett, K., L. K. Larkins, A. K. Das & A. K. Hajra. 1991. Peroxisomal localization of acyl-coenzyme A reductase (long chain alcohol forming) in guinea pig intestine mucosal cells. J. Biol. Chem. 26: 12201 – 12206.en_US
dc.identifier.citedreferenceBallas, L. M., P. B. Lazarow & R. M. Bell. 1984. Glycerolipid synthetic capacity of rat liver peroxisomes. Biochim. Biophys. Acta. 795: 297 – 300.en_US
dc.identifier.citedreferenceBell, R. M. & R. A. Coleman. 1980. Enzymes of glycerolipid synthesis in eukaryotes. Annu. Rev. Biochem. 49: 459 – 487.en_US
dc.identifier.citedreferenceHajra, A. K., S. Horie & K. O. Webber. 1988. The role of peroxisomes in glycerol ether lipid metabolism. Prgr. in Clin. Biol. Res. 282: 99 – 116.en_US
dc.identifier.citedreferenceBishop, J. E., M. Salem & A. K. Hajra. 1982. Topographical distribution of lipid biosynthetic enzymes on peroxisomes (microperoxisomes). Ann. N.Y. Acad. Sci. 386: 411 – 413.en_US
dc.identifier.citedreferenceGoldfischer, S., C. L. Moore, A. B. Johnson, A. J. Spiro, M. P. Valsamis, H. K. Wisniewski, R. H. Ritch, W. T. Norton, I. Rapin & L. M. Gartner. 1973. Peroxisomal and mitochondrial defects in the cerebro-hepato-renal syndrome. Science. 182: 62 – 64.en_US
dc.identifier.citedreferenceBorst, P. 1983. Animal peroxisomes (microbodies) lipid biosynthesis and Zellweger syndrome. Trends Biochem. Sci. 8: 269 – 272.en_US
dc.identifier.citedreferenceHeymans, H. S. A., R. B. H. Schutgens, R. Tan, H. van den Bosch & P. Borst. 1983. Severe plasmalogen deficiency in tissues of infants without peroxisomes (Zellweger syndrome). Nature. 306: 69 – 70.en_US
dc.identifier.citedreferenceLazarow, P., V. Black, A. K. Hajra, N. S. Datta, B. Bangaru & J. Dancis. 1984. Biochemical and morphological peroxisomal defects in Zellweger syndrome. J. Ped. Res. 18: 223a.en_US
dc.identifier.citedreferenceDatta, N. S., G. N. Wilson & A. K. Hajra. 1984. Deficiency of enzymes catalyzing the biosynthesis of glycerol-ether lipids in Zellweger syndrome. A new category of metabolic disease involving the absence of peroxisomes. New Engl. J. Med. 311: 1080 – 1083.en_US
dc.identifier.citedreferenceSchutgens, R. B., G. J. Romeyn, R. J. Wanders, H. van den Bosch, G. Schrakamp & H. S. Heymans. 1984. Deficiency of acyl-CoA: Dihydroxyacetone phosphate acyltransferase in patients with Zellweger (cerebro-hepato-renal) syndrome. Biochem. Biophys. Res. Commun. 120: 179 – 184.en_US
dc.identifier.citedreferenceKelley, R. I., A. B. Moser, A. K. Hajra, N. S. Datta, M. Noetzel, E. H. Zackai & H. Moser. 1986. Neonatal adrenoleukodystrophy: New cases, biochemical studies, and differentiation from Zellweger and related peroxisomal polydystrophy syndromes. Am. J. Med. Genetics. 23: 869 – 901.en_US
dc.identifier.citedreferencePoll-The, B. T., J. M. Saudubray, H. A. Ogier, M. Odievre, J. M. Scotto, L. Monnens, L. C. Govaerts, F. Roels, A. Cornelis & R. B. Schutgens. 1987. Infantile Refsum disease: An inherited peroxisomal disorder. Comparison with Zellweger syndrome and neonatal adrenoleukodystrophy. Eur. J. Pedatr. 146: 477 – 493.en_US
dc.identifier.citedreferenceHeymans, H. S., J. W. Oorthuys, G. Nelck, R. J. Wanders & R. B. Schutgens. 1985. Rhizomelic chondrodysplasia punctata: Another peroxisomal disorder. New Engl. J. Med. 313: 187 – 181.en_US
dc.identifier.citedreferenceHolmes, R. D., G. N. Wilson & A. K. Hajra. 1987. Peroxisomal enzyme deficiency in the Conradi-Hunerman form of chondrodysplasia punctata [letter]. New Engl. J. Med. 316: 1608.en_US
dc.identifier.citedreferenceHajra, A. K., N. S. Datta, G. L. Jackson, A. B. Moser, H. W. Moser, J. W. Larsen & J. Powers. 1985. Prenatal diagnosis of Zellweger cerebrohepatorenal syndrome [letter]. New Engl. J. Med. 312: 445 – 446.en_US
dc.identifier.citedreferenceWebber, K. O., N. S. Datta & A. K. Hajra. 1987. Properties of the enzymes catalyzing the biosynthesis of lysophosphatidate and its ether analog in cultured fibroblasts from Zellweger syndrome patients and normal controls. Arch. Biochem. Biophys. 254: 611 – 620.en_US
dc.identifier.citedreferenceLazarow, P. B. & H. W. Moser. 1989. In The Metabolic Basis of Inherited Disease, 6th ed. C. R. Scriver, A. L. Beaudet, W. S. Sly & D. Valle, Eds.: 1479 – 1509. McGraw-Hill. New York.en_US
dc.identifier.citedreferenceSantos, M. J., T. Imanaka, H. Shio & P. B. Lazarow. 1988. Peroxisomal integral membrane proteins in control and Zellweger fibroblasts. J. Biol. Chem. 263: 10502 – 10509.en_US
dc.identifier.citedreferenceJones, C. L. & A. K. Hajra. 1983. Solubilization and partial purification of dihydroxyacetone-phosphate acyltransferase from guinea pig liver. Arch. Biochem. Biophys. 226: 155 – 165.en_US
dc.identifier.citedreferenceWebber, K. O. & A. K. Hajra. 1992. Dihydroxyacetone phosphate acyltransferase. Meth. Enzymol. 209: 92 – 98.en_US
dc.identifier.citedreferenceWebber, K. O. & A. K. Hajra. 1993. Purification of dihydroxyacetone phosphate acyl-transferase from guinea pig liver peroxisomes. Arch. Biochem. Biophys. 300: 88 – 97.en_US
dc.identifier.citedreferenceOfman, R. & R. J. Wanders. 1994. Purification of peroxisomal acyl-CoA: Dihydroxyacetone phosphate acyltransferase from human placenta. Biochim. Biophys. Acta. 1206: 27 – 34.en_US
dc.identifier.citedreferenceBrown, A. J. & F. Snyder. 1983. The mechanism of alkyldihydroxyacetone-P synthase. J. Biol. Chem. 258: 4184 – 4189.en_US
dc.identifier.citedreferenceFriedberg, S. J. & M. Gomillion. 1981. Hydrogen exchange in the formation of dihydroxyacetone phosphate from acyl dihydroxyacetone phosphate in O -alkyl lipid synthesis in Ehrlich ascites tumor cell microsomes. J. Biol. Chem. 256: 291 – 295.en_US
dc.identifier.citedreferenceDavis, P. A. & A. K. Hajra. 1979. Stereochemical specificity of the biosynthesis of the alkyl ether bond in alkyl ether lipids. J. Biol. Chem. 254: 4760 – 4763.en_US
dc.identifier.citedreferenceHorie, S., A. K. Das & A. K. Hajra. 1992. Alkyldihydroxyacetonephosphate synthase from guinea pig liver peroxisomes. Methods Enzymol. 209: 385 – 390.en_US
dc.identifier.citedreferenceZomer, A. W., W. F. de Weerd, J. Langeveld & H. van den Bosch. 1993. Ether lipid synthesis: Purification and identification of alkyl dihydroxyacetone phosphate synthase from guinea-pig liver. Biochim. Biophys. Acta. 1170: 189 – 196.en_US
dc.identifier.citedreferenceTolbert, N. E. 1981. Metabolic pathways in peroxisomes and glyoxysomes. Annu. Rev. Biochem. 50: 133 – 157.en_US
dc.identifier.citedreferenceGutierrez, C., R. Okita & S. Krisans. 1988. Demonstration of cytochrome reductases in rat liver peroxisomes: Biochemical and immunochemical analyses. J. Lipid Res. 29: 613 – 628.en_US
dc.identifier.citedreferenceDas, A. K., S. Horie & A. K. Hajra. 1992. Biosynthesis of glycerolipid precursors in rat liver peroxisomes and their transport and conversion to phosphatidate in the endoplasmic reticulum. J. Biol. Chem. 267: 9724 – 9730.en_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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