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[Identification of the acyclic intermediate of nicotinic acid biosynthesis. IV. Conversion of the intermediate into epsilon-hydroxy-beta-carboxy-norleucine and beta-carboxy-lysine].

作者信息

Kuss E

出版信息

Hoppe Seylers Z Physiol Chem. 1967 Dec;348(12):1602-8.

PMID:5586907
Abstract
摘要

相似文献

1
[Identification of the acyclic intermediate of nicotinic acid biosynthesis. IV. Conversion of the intermediate into epsilon-hydroxy-beta-carboxy-norleucine and beta-carboxy-lysine].[烟酸生物合成中环状中间体的鉴定。IV. 中间体向ε-羟基-β-羧基正亮氨酸和β-羧基赖氨酸的转化]
Hoppe Seylers Z Physiol Chem. 1967 Dec;348(12):1602-8.
2
[Identification of the acyclic intermediate in nicotinic acid biosynthesis. II. Synthesis of diastereomers of epsilon-hydroxy-beta-carboxy-norleucine].
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3
[Identification of the acyclic intermediate in nicotinic acid biosynthesis. 3. Synthesis of beta-carboxy-lysine diastereomers].[烟酸生物合成中环状中间体的鉴定。3. β-羧基赖氨酸非对映异构体的合成]
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4
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5
[Proceedings: Acyclic intermediate product of enzymatic conversion of 3-hydroxyanthranilic acid into nicotinic acid].[会议论文：3-羟基邻氨基苯甲酸酶促转化为烟酸的无环中间产物]
Z Klin Chem Klin Biochem. 1972 Apr;10(4):177.
6
Synthesis and absolute configuration of the isomers of homoisocitric acid (1-hydroxy-1,2,4-butanetricarboxylic acid) and the stereochemistry of lysine biosynthesis.高异柠檬酸（1-羟基-1,2,4-丁三羧酸）异构体的合成、绝对构型及赖氨酸生物合成的立体化学
Biochemistry. 1969 Jul;8(7):2846-55. doi: 10.1021/bi00835a023.
7
[Biosynthesis of nicotinic acid and quinolinic acid by Mycobacterium bovis strain BCG].[卡介苗分枝杆菌合成烟酸和喹啉酸]
Arch Mikrobiol. 1970;75(1):80-8.
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[Acylation of primary amines with esters of dicarboxylic acid monophenylhydrazides].
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9
[Biosynthesis of nicotinic acid and quinolinic acid by Mycobacterium bovis strain BCG].[卡介苗分枝杆菌合成烟酸和喹啉酸]
Arch Mikrobiol. 1970;75(1):80-8.
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Quantification of azo-coupled lysine in azo proteins by amino acid analysis.通过氨基酸分析对偶氮蛋白中偶氮偶联赖氨酸进行定量分析。
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