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Conversion of alpha-aminoadipic acid to L-pipecolic acid by Aspergillus nidulans.

作者信息

ASPEN A J, MEISTER A

出版信息

Biochemistry. 1962 Jul;1:606-12. doi: 10.1021/bi00910a010.

DOI:10.1021/bi00910a010
PMID:13862932
Abstract
摘要

相似文献

1
Conversion of alpha-aminoadipic acid to L-pipecolic acid by Aspergillus nidulans.构巢曲霉将α-氨基己二酸转化为L-哌啶酸。
Biochemistry. 1962 Jul;1:606-12. doi: 10.1021/bi00910a010.
2
Metabolism of pipecolic acid in a Pseudomonas species. II. delta1-Piperideine-6-carboxylic acid and alpha-aminoadipic acid-delta-semial-dehyde.假单胞菌属中哌啶酸的代谢。II. δ1-哌啶-6-羧酸和α-氨基己二酸-δ-半醛。
J Biol Chem. 1962 Jul;237:2239-45.
3
Metabolic conversion of pipecolic acid to alpha-aminoadipic acid.哌啶酸向α-氨基己二酸的代谢转化。
J Biol Chem. 1962 Sep;237:2828-30.
4
Metabolism of pipecolic acid in a Pseudomonas species. I. alpha-Aminoadipic and glutamic acids.
J Biol Chem. 1962 Jul;237:2232-8.
5
Pyridine nucleotide-dependent reduction of the alpha-keto acid analogue of lysine to L-pipecolic acid.
Biochim Biophys Acta. 1957 Jan;23(1):202-3. doi: 10.1016/0006-3002(57)90308-6.
6
L-pipecolic acid metabolism in human liver: detection of L-pipecolate oxidase and identification of its reaction product.
Biochim Biophys Acta. 1990 May 8;1038(3):295-9. doi: 10.1016/0167-4838(90)90240-g.
7
A method for the quanitative determination of dehydropiperidine carboxylic acid, a reduction product of alpha-aminoadipic acid by yeast enzyme.一种定量测定脱氢哌啶羧酸的方法，它是α-氨基己二酸经酵母酶作用后的还原产物。
J Biochem. 1962 Jan;51:27-31. doi: 10.1093/oxfordjournals.jbchem.a127496.
8
Accumulation of S-sulphocysteine by a mutant strain of Aspergillus nidulans.构巢曲霉突变株对S-磺基半胱氨酸的积累
Nature. 1962 Feb 3;193:481-2. doi: 10.1038/193481a0.
9
6-Alkynyl- and 6-aryl-substituted (R)-pipecolic acid derivatives.6-炔基-和 6-芳基取代的（R）-哌啶酸衍生物。
Org Lett. 2013 Jun 7;15(11):2720-2. doi: 10.1021/ol4010728. Epub 2013 May 29.
10
[FORMATION OF CO2-14 FROM LABELED LYSINE, DELTA-1-PIPERIDINE-2-CARBOXYLIC ACID AND PIPECOLIC ACID IN THE "STERILE" RAT].["在“无菌”大鼠体内由标记的赖氨酸、δ-1-哌啶-2-羧酸和哌可酸形成二氧化碳-14"]
C R Hebd Seances Acad Sci. 1964 Jul 27;259:932-3.

引用本文的文献

1
Interconnected Set of Enzymes Provide Lysine Biosynthetic Intermediates and Ornithine Derivatives as Key Precursors for the Biosynthesis of Bioactive Secondary Metabolites.相互关联的酶系提供赖氨酸生物合成中间体和鸟氨酸衍生物，作为生物活性次生代谢物生物合成的关键前体。
Antibiotics (Basel). 2023 Jan 12;12(1):159. doi: 10.3390/antibiotics12010159.
2
Reciprocal Control of Thyroid Binding and the Pipecolate Pathway in the Brain.大脑中甲状腺结合与哌啶酸途径的相互调控
Neurochem Res. 2017 Jan;42(1):217-243. doi: 10.1007/s11064-016-2015-9. Epub 2016 Aug 12.
3
Lysine metabolism in mammalian brain: an update on the importance of recent discoveries.
哺乳动物大脑中的赖氨酸代谢：对近期发现重要性的更新。
Amino Acids. 2013 Dec;45(6):1249-72. doi: 10.1007/s00726-013-1590-1. Epub 2013 Sep 17.
4
Pipecolic acid in microbes: biosynthetic routes and enzymes.微生物中的哌啶酸：生物合成途径与酶
J Ind Microbiol Biotechnol. 2006 Jun;33(6):401-7. doi: 10.1007/s10295-006-0078-3. Epub 2006 Jan 18.
5
Inactivation of the lys7 gene, encoding saccharopine reductase in Penicillium chrysogenum, leads to accumulation of the secondary metabolite precursors piperideine-6-carboxylic acid and pipecolic acid from alpha-aminoadipic acid.在产黄青霉中，编码酵母氨酸还原酶的lys7基因失活，导致次生代谢物前体哌啶-6-羧酸和哌可酸从α-氨基己二酸积累。
Appl Environ Microbiol. 2004 Feb;70(2):1031-9. doi: 10.1128/AEM.70.2.1031-1039.2004.
6
Conversion of pipecolic acid into lysine in Penicillium chrysogenum requires pipecolate oxidase and saccharopine reductase: characterization of the lys7 gene encoding saccharopine reductase.产黄青霉中哌啶酸转化为赖氨酸需要哌啶酸氧化酶和酵母氨酸还原酶：编码酵母氨酸还原酶的lys7基因的特性分析。
J Bacteriol. 2001 Dec;183(24):7165-72. doi: 10.1128/JB.183.24.7165-7172.2001.
7
Lysine biosynthesis in Rhodotorula glutinis: properties of pipecolic acid oxidase.粘红酵母中赖氨酸的生物合成：哌啶酸氧化酶的特性
J Bacteriol. 1982 Sep;151(3):1073-7. doi: 10.1128/jb.151.3.1073-1077.1982.
8
Mutants of Saccharomycopsis lipolytica defective in lysine catabolism.解脂耶氏酵母赖氨酸分解代谢缺陷型突变体。
J Bacteriol. 1976 Jan;125(1):48-57. doi: 10.1128/jb.125.1.48-57.1976.
9
Role of pipecolic acid in the biosynthesis of lysine in Rhodotorula glutinis.哌啶酸在粘红酵母赖氨酸生物合成中的作用。
J Bacteriol. 1979 May;138(2):410-7. doi: 10.1128/jb.138.2.410-417.1979.