Literature DB >> 7410205

Mycinamicins, new macrolide antibiotics. I. Taxonomy, production, isolation, characterization and properties.

S Satoi, N Muto, M Hayashi, T Fujii, M Otani.   

Abstract

Mycinamicins, novel macrolide antibiotics were obtained from the culture broth of Micromonospora grisseorubida sp. nov. Isolation of five components, mycinamicins I, II, III, IV and V, was accomplished by silica gel adsorption or partition chromatography. Mycinsmicin I and II exhibit a strong UV absorption peak at 218 nm and have a shoulder at 240 nm. Mycinamicin III, IV and V show strong UV absorption peaks at 215 nm and around 280 nm. From their physicochemical and biological properties, the mycinamicins are classified as new macrolide antibiotics.

Entities:  

Mesh:

Substances:

Year:  1980        PMID: 7410205     DOI: 10.7164/antibiotics.33.364

Source DB:  PubMed          Journal:  J Antibiot (Tokyo)        ISSN: 0021-8820            Impact factor:   2.649


  22 in total

1.  The ecology of antibiotic production.

Authors:  S T Williams; J C Vickers
Journal:  Microb Ecol       Date:  1986-03       Impact factor: 4.552

2.  Functional analysis of MycCI and MycG, cytochrome P450 enzymes involved in biosynthesis of mycinamicin macrolide antibiotics.

Authors:  Yojiro Anzai; Shengying Li; Mani Raj Chaulagain; Kenji Kinoshita; Fumio Kato; John Montgomery; David H Sherman
Journal:  Chem Biol       Date:  2008-09-22

3.  A new structural form in the SAM/metal-dependent o‑methyltransferase family: MycE from the mycinamicin biosynthetic pathway.

Authors:  David L Akey; Shengying Li; Jamie R Konwerski; Laura A Confer; Steffen M Bernard; Yojiro Anzai; Fumio Kato; David H Sherman; Janet L Smith
Journal:  J Mol Biol       Date:  2011-08-23       Impact factor: 5.469

Review 4.  A comprehensive review of glycosylated bacterial natural products.

Authors:  Sherif I Elshahawi; Khaled A Shaaban; Madan K Kharel; Jon S Thorson
Journal:  Chem Soc Rev       Date:  2015-11-07       Impact factor: 54.564

5.  Substrate recognition by the multifunctional cytochrome P450 MycG in mycinamicin hydroxylation and epoxidation reactions.

Authors:  Shengying Li; Drew R Tietz; Florentine U Rutaganira; Petrea M Kells; Yojiro Anzai; Fumio Kato; Thomas C Pochapsky; David H Sherman; Larissa M Podust
Journal:  J Biol Chem       Date:  2012-09-05       Impact factor: 5.157

6.  Solution Conformations and Dynamics of Substrate-Bound Cytochrome P450 MycG.

Authors:  Drew R Tietz; Larissa M Podust; David H Sherman; Thomas C Pochapsky
Journal:  Biochemistry       Date:  2017-05-16       Impact factor: 3.162

Review 7.  Astonishing diversity of natural surfactants: 2. Polyether glycosidic ionophores and macrocyclic glycosides.

Authors:  Valery M Dembitsky
Journal:  Lipids       Date:  2005-03       Impact factor: 1.880

8.  Structural basis of substrate specificity and regiochemistry in the MycF/TylF family of sugar O-methyltransferases.

Authors:  Steffen M Bernard; David L Akey; Ashootosh Tripathi; Sung Ryeol Park; Jamie R Konwerski; Yojiro Anzai; Shengying Li; Fumio Kato; David H Sherman; Janet L Smith
Journal:  ACS Chem Biol       Date:  2015-02-26       Impact factor: 5.100

9.  Characterization and expression of a P-450-like mycinamicin biosynthesis gene using a novel Micromonospora-Escherichia coli shuttle cosmid vector.

Authors:  M Inouye; Y Takada; N Muto; T Beppu; S Horinouchi
Journal:  Mol Gen Genet       Date:  1994-11-15

10.  Production of rosamicin derivatives in Micromonospora rosaria by introduction of D-mycinose biosynthetic gene with PhiC31-derived integration vector pSET152.

Authors:  Yojiro Anzai; Yohei Iizaka; Wei Li; Naoki Idemoto; Shu-ichi Tsukada; Kazuo Koike; Kenji Kinoshita; Fumio Kato
Journal:  J Ind Microbiol Biotechnol       Date:  2009-05-02       Impact factor: 3.346

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.