Proteomics of FACS-sorted heterogeneous Corynebacterium glutamicum populations

Harst A, Albaum S, Bojarzyn T, Trötschel C, Poetsch A (2017)
Journal of Proteomics 160: 1-7.

Zeitschriftenaufsatz | Veröffentlicht| Englisch
 
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Autor/in
Harst, Andreas; Albaum, StefanUniBi ; Bojarzyn, Tanja; Trötschel, Christian; Poetsch, Ansgar
Abstract / Bemerkung
The metabolic status of individual cells in microbial cultures can differ, being relevant for biotechnology, environmental and medical microbiology. However, it is hardly understood in molecular detail due to limitations of current analytical tools. Here, we demonstrate that FACS in combination with proteomics can be used to sort and analyze cell populations based on their metabolic state. A previously established GFP reporter system was used to detect and sort single Corynebacterium glutamicum cells based on the concentration of branched chain amino acids (BCAA) using FACS. A proteomics workflow optimized for small cell numbers was used to quantitatively compare proteomes of a Delta aceE mutant, lacking functional pyruvate dehydrogenase (PD), and the wild type. About 800 proteins could be quantified from 1,000,000 cells. In the Delta aceE mutant BCAA production was coordinated with upregulation of the glyoxylate cycle and TCA cycle to counter the lack of acetyl CoA resulting from the deletion of aceE. Biological significance: Metabolic pathways in C glutamicum WT and Delta aceE, devoid of functional pyruvate dehydrogenase, were compared to understand proteome changes that contribute to the high production of branched chain amino acids (BCAA) in the Delta aceE strain. The data complements previous metabolome studies and corroborates the role of malate provided by the glyoxylate cycle and increased activity of glycolysis and pyruvate carboxylase reaction to replenish the TCA cycle. A slight increase in acetohydroxyacid synthase (ILV subunit B) substantiates the previously reported increased pyruvate pool in C. glutamicum Delta aceE, and the benefit of additional ilv gene cluster overexpression for BCAA production. (C) 2017 Elsevier B.V. All rights reserved.
Stichworte
Corynebacterium glutamicum; BCAA producer; Cellular heterogeneity; FACS; Proteome analysis; Label-free quantification
Erscheinungsjahr
2017
Zeitschriftentitel
Journal of Proteomics
Band
160
Seite(n)
1-7
ISSN
1874-3919
eISSN
1876-7737
Page URI
https://pub.uni-bielefeld.de/record/2916543

Zitieren

Harst A, Albaum S, Bojarzyn T, Trötschel C, Poetsch A. Proteomics of FACS-sorted heterogeneous Corynebacterium glutamicum populations. Journal of Proteomics. 2017;160:1-7.
Harst, A., Albaum, S., Bojarzyn, T., Trötschel, C., & Poetsch, A. (2017). Proteomics of FACS-sorted heterogeneous Corynebacterium glutamicum populations. Journal of Proteomics, 160, 1-7. doi:10.1016/j.jprot.2017.03.010
Harst, A., Albaum, S., Bojarzyn, T., Trötschel, C., and Poetsch, A. (2017). Proteomics of FACS-sorted heterogeneous Corynebacterium glutamicum populations. Journal of Proteomics 160, 1-7.
Harst, A., et al., 2017. Proteomics of FACS-sorted heterogeneous Corynebacterium glutamicum populations. Journal of Proteomics, 160, p 1-7.
A. Harst, et al., “Proteomics of FACS-sorted heterogeneous Corynebacterium glutamicum populations”, Journal of Proteomics, vol. 160, 2017, pp. 1-7.
Harst, A., Albaum, S., Bojarzyn, T., Trötschel, C., Poetsch, A.: Proteomics of FACS-sorted heterogeneous Corynebacterium glutamicum populations. Journal of Proteomics. 160, 1-7 (2017).
Harst, Andreas, Albaum, Stefan, Bojarzyn, Tanja, Trötschel, Christian, and Poetsch, Ansgar. “Proteomics of FACS-sorted heterogeneous Corynebacterium glutamicum populations”. Journal of Proteomics 160 (2017): 1-7.

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