BIOSYNTHETIC ORIGIN OF AMINOBENZENOID NUCLEUS (C7N-UNIT) OF ANSAMITOCIN, A GROUP OF NOVEL MAYTANSINOID ANTIBIOTICS

被引：51

作者：

HATANO, K ^{[1
]}

AKIYAMA, SI ^{[1
]}

ASAI, M ^{[1
]}

RICKARDS, RW ^{[1
]}

机构：

[1] AUSTRALIAN NATL UNIV,RES SCH CHEM,CANBERRA,ACT 2600,AUSTRALIA

来源：

JOURNAL OF ANTIBIOTICS | 1982年 / 35卷 / 10期

关键词：

D O I：

10.7164/antibiotics.35.1415

中图分类号：

Q81 [生物工程学（生物技术）]; Q93 [微生物学];

学科分类号：

071005 ; 0836 ; 090102 ; 100705 ;

摘要：

引用

页码：1415 / 1417

页数：3

共 10 条

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[6] A GENETIC APPROACH TO THE BIOSYNTHESIS OF THE RIFAMYCIN-CHROMOPHORE IN NOCARDIA-MEDITERRANEI .4. IDENTIFICATION OF 3-AMINO-5-HYDROXYBENZOIC ACID AS A DIRECT PRECURSOR OF THE 7-CARBON AMINO STARTER-UNIT [J].

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[8] ANSAMITOCIN, A GROUP OF NOVEL MAYTANSINOID ANTIBIOTICS WITH ANTITUMOUR PROPERTIES FROM NOCARDIA [J].

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[9] 3-AMINO-5-HYDROXYBENZOIC ACID AS A KEY INTERMEDIATE IN ANSAMYCIN AND MAYTANSINOID BIOSYNTHESIS [J].

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[10] DIRECT EVIDENCE FROM MULTIPLE C-13 LABELING AND HOMONUCLEAR DECOUPLING FOR THE LABELING PATTERN BY GLUCOSE OF THE M-AMINOBENZOYL (C7N) UNIT OF PACTAMYCIN [J].

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