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Stereochemical course of enoyl reduction catalyzed by fatty acid synthetase. Stereochemistry of hydrogen incorporation from reduced pyridine nucleotide.

Stereochemical course of enoyl reduction catalyzed by fatty acid synthetase. Stereochemistry of hydrogen incorporation from reduced pyridine nucleotide. Research Abstract Details 

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  • Stereochemical course of enoyl reduction catalyzed by fatty acid synthetase. Stereochemistry of hydrogen incorporation from reduced pyridine nucleotide. Abstract Text:

    a kawaguchiA Kawaguchi,t yoshimuraT Yoshimura,k saitoK Saito,y seyamaY Seyama,t kasamaT Kasama,t yamakawaT Yamakawa,s okudaS Okuda,

    The stereochemical course of the enoyl reduction catalyzed by fatty acid synthetase was investigated using the enzymes from rat liver and Brevibacterium ammoniagenes. Deuterium-labeled fatty acids were synthesized by incubating the synthetases with either 4R-[4-2H1]- or 4S-[4-2H1]NADPH. The deuterium-labeled fatty acids thus produced were subjected to the action of a stereospecific enzyme, acyl-CoA oxidase. The deuterium-labeled fatty acids and 2,3-dehydroacyl thioesters, the products of acyl-CoA oxidase, were methylated and analyed for deuterium content by gas chromatography-mass spectrometry. These experiments provided information to determine the configuration at the C-3 position of fatty acids formed by fatty acid synthetases. The results suggested that the stereochemistry of hydrogen (as hydride) incorporation from reduced pyridine nucleotides during enoyl reduction was different between rat liver and B. ammoniagenes synthetases: the enoyl reduction of rat liver enzyme involved the re-attack of hydride and that of B. ammoniagenes enzyme involved the si-attack of hydride.

    Stereochemical course of enoyl reduction catalyzed by fatty acid synthetase. Stereochemistry of hydrogen incorporation from reduced pyridine nucleotide. Publishing Authors By Initials

    a kawaguchiA Kawaguchi,t yoshimuraT Yoshimura,k saitoK Saito,y seyamaY Seyama,t kasamaT Kasama,t yamakawaT Yamakawa,s okudaS Okuda,

    For similar tritium research abstracts see: tritium research

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    Stereochemical course of enoyl reduction catalyzed by fatty acid synthetase. Stereochemistry of hydrogen incorporation from reduced pyridine nucleotide. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Journal of biochemistry

    VOLUME: 88

    Page Numbers: 1-7

    Journal Abbreviation: J. Biochem.

    ISSN: 0021-924X

    DAY: 19

    MONTH: Jul

    YEAR: 1980

    Stereochemical course of enoyl reduction catalyzed by fatty acid synthetase. Stereochemistry of hydrogen incorporation from reduced pyridine nucleotide. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 376600

    Stereochemical course of enoyl reduction catalyzed by fatty acid synthetase. Stereochemistry of hydrogen incorporation from reduced pyridine nucleotide. Keywords Mesh Terms:

    KEYWORDS: Tritium

    MESH TERMS: metabolism

    Chemical & Substance for Abstract: Stereochemical course of enoyl reduction catalyzed by fatty acid synthetase. Stereochemistry of hydrogen incorporation from reduced pyridine nucleotide. Information

    Substance Name: Fatty Acid Synthetase Complex

    Registry Number: EC 6.-

    Grant and Affiliation Information for Stereochemical course of enoyl reduction catalyzed by fatty acid synthetase. Stereochemistry of hydrogen incorporation from reduced pyridine nucleotide.

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    Country: JAPAN

    JAPAN Research PublicationJAPAN Research Publication

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    MEDLINETA: J Biochem

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