| Literature DB >> 22641157 |
David J Gonzalez1, Yuquan Xu2, Yu-Liang Yang2, Eduardo Esquenazi3, Wei-Ting Liu4, Anna Edlund5, Tram Duong2, Liangcheng Du6, István Molnár7, William H Gerwick5, Paul R Jensen5, Michael Fischbach8, Chih-Chuang Liaw9, Paul Straight10, Victor Nizet1, Pieter C Dorrestein11.
Abstract
Many microbes can be cultured as single-species communities. Often, these colonies are controlled and maintained via the secretion of metabolites. Such metabolites have been an invaluable resource for the discovery of therapeutics (e.g. penicillin, taxol, rapamycin, epothilone). In this article, written for a special issue on imaging mass spectrometry, we show that MALDI-imaging mass spectrometry can be adapted to observe, in a spatial manner, the metabolic exchange patterns of a diverse array of microbes, including thermophilic and mesophilic fungi, cyanobacteria, marine and terrestrial actinobacteria, and pathogenic bacteria. Dependent on media conditions, on average and based on manual analysis, we observed 11.3 molecules associated with each microbial IMS experiment, which was split nearly 50:50 between secreted and colony-associated molecules. The spatial distributions of these metabolic exchange factors are related to the biological and ecological functions of the organisms. This work establishes that MALDI-based IMS can be used as a general tool to study a diverse array of microbes. Furthermore the article forwards the notion of the IMS platform as a window to discover previously unreported molecules by monitoring the metabolic exchange patterns of organisms when grown on agar substrates. Published by Elsevier B.V.Entities:
Mesh:
Year: 2012 PMID: 22641157 PMCID: PMC3543690 DOI: 10.1016/j.jprot.2012.05.036
Source DB: PubMed Journal: J Proteomics ISSN: 1874-3919 Impact factor: 4.044