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产碳青霉烯类抗生素的OA-6129阻断突变体的诱变及碳青霉烯类抗生素的生物合成。

Mutagenesis of OA-6129 carbapenem-producing blocked mutants and the biosynthesis of carbapenems.

作者信息

Kojima I, Fukagawa Y, Okabe M, Ishikura T, Shibamoto N

机构信息

Sanraku Incorporated, Central Research Laboratories, Fujisawa, Japan.

出版信息

J Antibiot (Tokyo). 1988 Jul;41(7):899-907. doi: 10.7164/antibiotics.41.899.

DOI:10.7164/antibiotics.41.899
PMID:3417564
Abstract

Streptomyces fulvoviridis A933 17M9 1501 is an A933 acylase-defective mutant derived from S. fulvoviridis A933 17M9 and thus produces the OA-6129 group of carbapenems and carbapenams. By further mutation of mutant 1501, 4 types of mutants (OA-6129 A + B1 + B2 producers; OA-6129 A + B2 producers; an OA-6129 A producer; non-producers) were obtained. The second type of mutant strains 4N 3607, 5NA 3949-40 and 5NE 252 proved useful for the fermentative production of carbapenem OA-6129 B2. These results of mutagenesis demonstrated that the sequence of carbapenem bioconversion in the horizontal route was hydroxylation at C-8----isomerization at C-6----sulfation at C-8 hydroxyl.

摘要

黄绿链霉菌A933 17M9 1501是源自黄绿链霉菌A933 17M9的A933酰基转移酶缺陷型突变体,因此可产生OA - 6129组碳青霉烯类和碳青霉烯胺类。通过对突变体1501的进一步诱变,获得了4种类型的突变体(OA - 6129 A + B1 + B2产生菌;OA - 6129 A + B2产生菌;OA - 6129 A产生菌;不产生菌)。第二类突变株4N 3607、5NA 3949 - 40和5NE 252被证明可用于碳青霉烯类OA - 6129 B2的发酵生产。这些诱变结果表明,水平途径中碳青霉烯生物转化的顺序为C - 8位羟基化→C - 6位异构化→C - 8位羟基硫酸化。

相似文献

1
Mutagenesis of OA-6129 carbapenem-producing blocked mutants and the biosynthesis of carbapenems.产碳青霉烯类抗生素的OA-6129阻断突变体的诱变及碳青霉烯类抗生素的生物合成。
J Antibiot (Tokyo). 1988 Jul;41(7):899-907. doi: 10.7164/antibiotics.41.899.
2
Studies on the biosynthesis of carbapenem antibiotics. I. Biosynthetic significance of the OA-6129 group of carbapenem compounds as the direct precursors for PS-5, epithienamycins A and C and MM 17880.
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Studies on the biosynthesis of carbapenem antibiotics. II. Isolation and functions of a specific acylase involved in the depantothenylation of the OA-6129 compounds.碳青霉烯类抗生素的生物合成研究。II. 参与OA - 6129化合物去泛酰基化反应的一种特异性酰基转移酶的分离及其功能
J Antibiot (Tokyo). 1984 Nov;37(11):1394-402. doi: 10.7164/antibiotics.37.1394.
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Studies on the biosynthesis of carbapenem antibiotics. III. Enzymological characterization of the L-amino acid acylase activity of A933 acylase.碳青霉烯类抗生素的生物合成研究。III. A933酰基转移酶L-氨基酸酰基转移酶活性的酶学特性
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Studies on the biosynthesis of carbapenem antibiotics. IV. Beta-alanine in the C-3 pantetheinyl side chain of the OA-6129 group of carbapenems.碳青霉烯类抗生素的生物合成研究。IV. OA - 6129组碳青霉烯类抗生素C-3泛酰硫乙胺侧链中的β-丙氨酸
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FEMS Microbiol Lett. 1989 Jan 1;48(1):51-5. doi: 10.1016/0378-1097(89)90145-6.
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Microbial phosphorylation of the OA-6129 group of carbapenem compounds.碳青霉烯类化合物OA - 6129组的微生物磷酸化作用。
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J Antibiot (Tokyo). 1983 Nov;36(11):1473-82. doi: 10.7164/antibiotics.36.1473.
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J Antibiot (Tokyo). 1982 Oct;35(10):1255-63. doi: 10.7164/antibiotics.35.1255.

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