A Technical Platform for Generating Reproducible Expression Data from Streptomyces coelicolor Batch Cultivations

被引:6
|
作者
Battke, F. [2 ]
Herbig, A. [2 ]
Wentzel, A. [3 ,4 ]
Jakobsen, O. M. [3 ]
Bonin, M. [5 ]
Hodgson, D. A. [6 ]
Wohlleben, W. [7 ]
Ellingsen, T. E. [3 ]
Nieselt, K. [1 ]
机构
[1] Univ Tubingen, Fac Sci, Ctr Bioinformat Tubingen, D-72076 Tubingen, Germany
[2] Univ Tubingen, Dept Informat & Cognit Sci, Ctr Bioinformat Tubingen, D-72076 Tubingen, Germany
[3] SINTEF Mat & Chem, Dept Biotechnol, N-7465 Trondheim, Norway
[4] Norwegian Univ Sci & Technol NTNU, Dept Biotechnol, N-7491 Trondheim, Norway
[5] Microarray Facil Tubingen, D-72076 Tubingen, Germany
[6] Univ Warwick, Dept Biol Sci, Coventry CV4 7AL, W Midlands, England
[7] Univ Tubingen, Dept Microbiol Biotechnol, D-72076 Tubingen, Germany
基金
英国生物技术与生命科学研究理事会;
关键词
Batch fermentation; Chromosomal gene clusters; Microarray design; Streptomyces coelicolor; PHOP; IDENTIFICATION; BINDING; GENES;
D O I
10.1007/978-1-4419-7046-6_1
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Streptomyces coelicolor, the model species of the genus Streptomyces, presents a complex life cycle of successive morphological and biochemical changes involving the formation of substrate and aerial mycelium, sporulation and the production of antibiotics. The switch from primary to secondary metabolism can be triggered by nutrient starvation and is of particular interest as some of the secondary metabolites produced by related Streptomycetes are commercially relevant. To understand these events on a molecular basis, a reliable technical platform encompassing reproducible fermentation as well as generation of coherent transcriptomic data is required. Here, we investigate the technical basis of a previous study as reported by Nieselt et at (BMC Genomics 11:10, 2010) in more detail, based on the same samples and focusing on the validation of the custom-designed rnicroarray as well as on the reproducibility of the data generated from biological replicates. We show that the protocols developed result in highly coherent transcriptomic measurements. Furthermore, we use the data to predict chromosomal gene clusters, extending previously known clusters as well as predicting interesting new clusters with consistent functional annotations.
引用
收藏
页码:3 / 15
页数:13
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