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间型霉素的生物合成。由间型霉素B形成间型霉素。

Biosynthesis of formycin. Formation of formycin from formycin B.

作者信息

Ochi D, Yashima S, Eguchi Y

出版信息

J Antibiot (Tokyo). 1975 Dec;28(12):965-73. doi: 10.7164/antibiotics.28.965.

DOI:10.7164/antibiotics.28.965
PMID:1206009
Abstract
  1. In replacement culture with a formycin-producing strain. Steptomyces sp. MA406-A-1, exogenously added formycin B was quantitatively converted to formycin and the conversion was inhibited by adding the chromophore moiety of formycin. 2. The in vitro experiments revealed that the novel enzyme(s) catalyzing the formation and formycin from asparate and formycin B, but not from formycin B monophosphate, was present in this organism. The action of the partially purified enzyme(s) was also inhibited by the chromophore moiety of formycin, whereas the moiety showed no inhibitory effect on the actions of adenylosuccinate synthetase and adenylosuccinate lyase. 3. Adenine auxotrophs lacking either adenylosuccinate synthetase or adrenylosuccinate lyase were derived from strain MA406-A-1 and these auxotrophs were found to readily convert formycin B to formycin in replacement culture. From these results, it was estimated that, under the conditions of replacement culture, formycin B would be converted to formycin in vivo by the action of novel enzyme(s) rather than by the action of enzyme system including adenylosuccinate synthetase and adenylosuccinate lyase.
摘要
  1. 在使用产间型霉素菌株链霉菌属MA406 - A - 1进行补充培养时,外源添加的间型霉素B被定量转化为间型霉素,并且添加间型霉素的发色团部分可抑制这种转化。2. 体外实验表明,该生物体中存在一种新型酶,可催化由天冬氨酸和间型霉素B形成间型霉素,但不能由间型霉素B单磷酸形成间型霉素。部分纯化的酶的作用也受到间型霉素发色团部分的抑制,而该部分对腺苷酸琥珀酸合成酶和腺苷酸琥珀酸裂解酶的作用没有抑制作用。3. 从菌株MA406 - A - 1获得了缺乏腺苷酸琥珀酸合成酶或腺苷酸琥珀酸裂解酶的腺嘌呤营养缺陷型菌株,发现这些营养缺陷型菌株在补充培养中能轻易地将间型霉素B转化为间型霉素。根据这些结果估计,在补充培养条件下,间型霉素B在体内将通过新型酶的作用而非包括腺苷酸琥珀酸合成酶和腺苷酸琥珀酸裂解酶的酶系统的作用转化为间型霉素。

相似文献

1
Biosynthesis of formycin. Formation of formycin from formycin B.间型霉素的生物合成。由间型霉素B形成间型霉素。
J Antibiot (Tokyo). 1975 Dec;28(12):965-73. doi: 10.7164/antibiotics.28.965.
2
Biosynthesis of formycin. Incorporation and distribution of labeled compounds into formycin.间型霉素的生物合成。标记化合物掺入间型霉素及其分布。
J Antibiot (Tokyo). 1976 Jun;29(6):638-45. doi: 10.7164/antibiotics.29.638.
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Biosynthesis of formycin. Role of certain amino acids in formycin biosynthesis.间型霉素的生物合成。某些氨基酸在间型霉素生物合成中的作用。
J Antibiot (Tokyo). 1974 Dec;27(12):909-16. doi: 10.7164/antibiotics.27.909.
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Biosynthesis of formycin. Incorporation and distribution of 13C-, 14C-, and 15N-labeled compounds into formycin.间型霉素的生物合成。13C、14C和15N标记化合物掺入间型霉素及其分布。
J Biol Chem. 1979 Sep 25;254(18):8819-24.
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A decrease in GTP content is associated with aerial mycelium formation in Streptomyces MA406-A-1.鸟苷三磷酸(GTP)含量的降低与链霉菌MA406 - A - 1中气生菌丝体的形成有关。
J Gen Microbiol. 1986 Feb;132(2):299-305. doi: 10.1099/00221287-132-2-299.
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Monophosphates of formycin B and allopurinol riboside. Interactions with leishmanial and mammalian succino-AMP synthetase and GMP reductase.间型霉素B和别嘌呤醇核苷的单磷酸盐。与利什曼原虫和哺乳动物琥珀酸-AMP合成酶及GMP还原酶的相互作用。
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Identification and Characterization of Enzymes Catalyzing Pyrazolopyrimidine Formation in the Biosynthesis of Formycin A.鉴定和表征在福米卡汀生物合成中催化吡唑并嘧啶形成的酶。
Org Lett. 2017 Mar 17;19(6):1426-1429. doi: 10.1021/acs.orglett.7b00355. Epub 2017 Feb 24.
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The effect of formycin B on mRNA translation and uptake of purine precursors in Leishmania mexicana.间型霉素B对墨西哥利什曼原虫mRNA翻译及嘌呤前体摄取的影响。
Biochem Int. 1984 Aug;9(2):207-18.
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Action of tubercidin and other adenosine analogs on Schistosoma mansoni schistosomules.结核菌素及其他腺苷类似物对曼氏血吸虫童虫的作用。
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Identification of the Formycin A Biosynthetic Gene Cluster from Streptomyces kaniharaensis Illustrates the Interplay between Biological Pyrazolopyrimidine Formation and de Novo Purine Biosynthesis.从链霉菌中鉴定出的(formycin A)生物合成基因簇阐明了生物吡唑并嘧啶形成和从头嘌呤生物合成之间的相互作用。
J Am Chem Soc. 2019 Apr 17;141(15):6127-6131. doi: 10.1021/jacs.9b00241. Epub 2019 Apr 8.

引用本文的文献

1
Identification of the Formycin A Biosynthetic Gene Cluster from Streptomyces kaniharaensis Illustrates the Interplay between Biological Pyrazolopyrimidine Formation and de Novo Purine Biosynthesis.从链霉菌中鉴定出的(formycin A)生物合成基因簇阐明了生物吡唑并嘧啶形成和从头嘌呤生物合成之间的相互作用。
J Am Chem Soc. 2019 Apr 17;141(15):6127-6131. doi: 10.1021/jacs.9b00241. Epub 2019 Apr 8.