22.11.2012 Aufrufe

FORTSCHRITTSBERICHT JAHR 2006 - Helmholtz-Zentrum für ...

FORTSCHRITTSBERICHT JAHR 2006 - Helmholtz-Zentrum für ...

FORTSCHRITTSBERICHT JAHR 2006 - Helmholtz-Zentrum für ...

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Entwicklungen auf <strong>Zentrum</strong>sebene<br />

JRG Structure and Function of Antibiotics (SFA)<br />

Head: Dr. Dirk Menche<br />

Research in this group is centred around various aspects of natural product chemistry and antiinfective<br />

research, ranging from natural product isolation, the development of new synthetic<br />

methods to novel strategies in natural product synthesis, and analogue design. A particular<br />

emphasis is placed on novel antimalarial structures from African medicinal plants. Another<br />

major activity is directed towards novel methodologies to synthesize chiral amines, key structural<br />

elements of a multitude of antiinfectives, in only one chemical (stereoselective) transformation<br />

from readily available building blocks.<br />

RG Microbial Drugs (MWI)<br />

Head: Prof. Dr. Rolf Müller<br />

The research group aims to mine genomic information and biodiversity for the production of<br />

novel and altered natural products with various biological activities. Using molecular biological<br />

tools under development for gliding bacteria and having various genome data plus a most<br />

important myxobacterial strain collection at hand, the enormous genomic potential to make<br />

novel metabolites will be exploited. Biosynthetic as well as fermentation studies of known<br />

compounds are performed to provide substances for further development and increase/alter<br />

production in natural hosts. Enzymes involved in the respective biosynthesis are used in<br />

chemoenzymatic approaches to enable natural product syntheses. Uncommon habitats are<br />

screened for the presence of novel classes of gliding bacteria to provide new sources for lead<br />

structures for the screening process. In parallel, tools are developed to heterologously produce<br />

valuable compounds in more ameneable foreign host organisms.<br />

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