Literature DB >> 25798711

Isolation, biological activity, biosynthesis and synthetic studies towards the rubromycin family of natural products.

Darcy J Atkinson1, Margaret A Brimble.   

Abstract

The rubromycins are an ever growing family of natural products isolated from various Actinomycetes over the last 60 years. Exhibiting a highly attractive array of antimicrobial and enzyme activity, this unique family of compounds have attracted significant attention from many synthetic chemists. Investigations into the synthesis of the densely functionalised hexacyclic ring system have revealed many hidden synthetic challenges. This review covers the isolation, the reported biological activity and the detailed synthetic studies towards these complex natural products.

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Year:  2015        PMID: 25798711     DOI: 10.1039/c4np00153b

Source DB:  PubMed          Journal:  Nat Prod Rep        ISSN: 0265-0568            Impact factor:   13.423


  12 in total

1.  Absolute Configurations of Griseorhodins A and C.

Authors:  Humberto E Ortega; João M Batista; Weilan G P Melo; Jon Clardy; Mônica T Pupo
Journal:  Tetrahedron Lett       Date:  2017-11-07       Impact factor: 2.415

2.  Lewis Base Catalyzed, Sulfenium Ion Initiated Enantioselective, Spiroketalization Cascade.

Authors:  Kimberly M Hilby; Scott E Denmark
Journal:  J Org Chem       Date:  2021-10-21       Impact factor: 4.354

3.  An acetyltransferase controls the metabolic flux in rubromycin polyketide biosynthesis by direct modulation of redox tailoring enzymes.

Authors:  Marina Toplak; Adelheid Nagel; Britta Frensch; Thorsten Lechtenberg; Robin Teufel
Journal:  Chem Sci       Date:  2022-05-17       Impact factor: 9.969

4.  Structure Determination, Functional Characterization, and Biosynthetic Implications of Nybomycin Metabolites from a Mining Reclamation Site-Associated Streptomyces.

Authors:  Xiachang Wang; Sherif I Elshahawi; Larissa V Ponomareva; Qing Ye; Yang Liu; Gregory C Copley; James C Hower; Bruce E Hatcher; Madan K Kharel; Steven G Van Lanen; Qing-Bai She; S Randal Voss; Jon S Thorson; Khaled A Shaaban
Journal:  J Nat Prod       Date:  2019-12-13       Impact factor: 4.050

5.  Designed Spiroketal Protein Modulation.

Authors:  Marcel Scheepstra; Sebastian A Andrei; M Yagiz Unver; Anna K H Hirsch; Seppe Leysen; Christian Ottmann; Luc Brunsveld; Lech-Gustav Milroy
Journal:  Angew Chem Int Ed Engl       Date:  2017-04-13       Impact factor: 15.336

6.  Enzymatic spiroketal formation via oxidative rearrangement of pentangular polyketides.

Authors:  Britta Frensch; Thorsten Lechtenberg; Michel Kather; Zeynep Yunt; Martin Betschart; Bernd Kammerer; Steffen Lüdeke; Michael Müller; Jörn Piel; Robin Teufel
Journal:  Nat Commun       Date:  2021-03-04       Impact factor: 14.919

7.  Chemical genetic approach using β-rubromycin reveals that a RIO kinase-like protein is involved in morphological development in Phytophthora infestans.

Authors:  Shuji Tani; Naotaka Nishio; Kenji Kai; Daisuke Hagiwara; Yoshiyuki Ogata; Motoaki Tojo; Jun-Ichi Sumitani; Howard S Judelson; Takashi Kawaguchi
Journal:  Sci Rep       Date:  2020-12-18       Impact factor: 4.379

8.  Draft Genome Sequence of an Anthracimycin Producer, Streptomyces sp. TP-A0875.

Authors:  Hisayuki Komaki; Natsuko Ichikawa; Akira Hosoyama; Nobuyuki Fujita; Enjuro Harunari; Yasuhiro Igarashi
Journal:  Genome Announc       Date:  2015-10-08

Review 9.  Biosynthesis and molecular actions of specialized 1,4-naphthoquinone natural products produced by horticultural plants.

Authors:  Joshua R Widhalm; David Rhodes
Journal:  Hortic Res       Date:  2016-09-21       Impact factor: 6.793

10.  A comparative metabologenomic approach reveals mechanistic insights into Streptomyces antibiotic crypticity.

Authors:  Yunci Qi; Keshav K Nepal; Joshua A V Blodgett
Journal:  Proc Natl Acad Sci U S A       Date:  2021-08-03       Impact factor: 11.205

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