Biosynthesis of methyl-proline containing griselimycins, natural products with anti-tuberculosis activity

Author:

Lukat Peer12345,Katsuyama Yohei12345,Wenzel Silke12345,Binz Tina12345ORCID,König Claudia6785,Blankenfeldt Wulf91011512ORCID,Brönstrup Mark1310115ORCID,Müller Rolf12345ORCID

Affiliation:

1. Helmholtz Institute for Pharmaceutical Research Saarland (HIPS)

2. Helmholtz Center for Infection Research and Pharmaceutical Biotechnology

3. Saarland University Campus

4. 66123 Saarbrücken

5. Germany

6. Sanofi Aventis Deutschland

7. Industriepark Höchst

8. 65926 Frankfurt

9. Structure and Function of Proteins

10. Helmholtz Centre for Infection Research

11. 38124 Braunschweig

12. Institute of Biochemistry, Biotechnology and Bioinformatics

13. Department for Chemical Biology

Abstract

The biosynthesis of griselimycins in Streptomyces DSM 40835 and the pathway that stereospecifically converts l-leucine to (2S,4R)-4-methyl-proline are reported by means of biochemical and structural analysis.

Funder

BMBF

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Reference20 articles.

1. Global Tuberculosis Report 2015, World Health Organization, Geneva, Switzerland, 2015

2. F. Bénazet , in Antibiotics: Advances in Research : Proceedings of the Congress on Antibiotics Held in Prague, 15–19 June 1964, ed. M. Herold and Z. Gabriel, Butterworths, 1966

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