Spontaneity in the patellamide biosynthetic pathway
- 9 January 2006
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Organic & Biomolecular Chemistry
- Vol. 4 (4), 631-638
- https://doi.org/10.1039/b515938e
Abstract
Post-translationally modified ribosomal peptides are unusual natural products and many have potent biological activity. The biosynthetic processes involved in their formation have been delineated for some, but the patellamides represent a unique group of these metabolites with a combination of a macrocycle, small heterocycles and D-stereocentres. The genes encoding for the patellamides show very low homology to known biosynthetic genes and there appear to be no explicit genes for the macrocyclisation and epimerisation steps. Using a combination of literature data and large-scale molecular dynamics calculations with explicit solvent, we propose that the macrocyclisation and epimerisation steps are spontaneous and interdependent and a feature of the structure of the linear peptide. Our study suggests the steps in the biosynthetic route are heterocyclisation, macrocyclisation, followed by epimerisation and finally dehydrogenation. This study is presented as testable hypothesis based on literature and theoretical data to be verified by future detailed experimental investigations.Keywords
This publication has 36 references indexed in Scilit:
- Biosynthesis and Mode of Action of LantibioticsChemical Reviews, 2005
- Pseudoprolines as Removable Turn Inducers: Tools for the Cyclization of Small PeptidesThe Journal of Organic Chemistry, 2004
- Conformational change in the thiazole and oxazoline containing cyclic octapeptides, the patellamides. Part 2. Solvent dependent conformational changeElectronic supplementary information (ESI) available: further calculational details. See http://www.rsc.org/suppdata/p2/b2/b201824c/Journal of the Chemical Society, Perkin Transactions 2, 2002
- Conformational Studies and Structure−Activity Analysis of Lissoclinamide 7 and Related Cyclopeptide AlkaloidsJournal of the American Chemical Society, 1998
- Specific Interaction of Wild-Type and Truncated Mouse N-Methylpurine-DNA Glycosylase with Ethenoadenine-Containing DNABiochemistry, 1998
- GROMACS: A message-passing parallel molecular dynamics implementationComputer Physics Communications, 1995
- CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choiceNucleic Acids Research, 1994
- A molecular dynamics study of the decane/water interfaceThe Journal of Physical Chemistry, 1993
- The endiandric acid cascade. Electrocyclizations in organic synthesis. 4. Biomimetic approach to endiandric acids A-G. Total synthesis and thermal studiesJournal of the American Chemical Society, 1982
- Postulated electrocyclic reactions leading to endiandric acid and related natural productsJournal of the Chemical Society, Chemical Communications, 1980