Helmholtz Gemeinschaft

Search
Browse
Statistics
Feeds

Metabolite interactions in the bacterial Calvin cycle and implications for flux regulation

[img]
Preview
PDF (Original Article) - Requires a PDF viewer such as GSview, Xpdf or Adobe Acrobat Reader
4MB
[img] Other (Supplementary Information)
13MB

Item Type:Article
Title:Metabolite interactions in the bacterial Calvin cycle and implications for flux regulation
Creators Name:Sporre, E. and Karlsen, J. and Schriever, K. and Asplund-Samuelsson, J. and Janasch, M. and Strandberg, L. and Karlsson, A. and Kotol, D. and Zeckey, L. and Piazza, I. and Syrén, P.O. and Edfors, F. and Hudson, E.P.
Abstract:Metabolite-level regulation of enzyme activity is important for microbes to cope with environmental shifts. Knowledge of such regulations can also guide strain engineering for biotechnology. Here we apply limited proteolysis-small molecule mapping (LiP-SMap) to identify and compare metabolite-protein interactions in the proteomes of two cyanobacteria and two lithoautotrophic bacteria that fix CO(2) using the Calvin cycle. Clustering analysis of the hundreds of detected interactions shows that some metabolites interact in a species-specific manner. We estimate that approximately 35% of interacting metabolites affect enzyme activity in vitro, and the effect is often minor. Using LiP-SMap data as a guide, we find that the Calvin cycle intermediate glyceraldehyde-3-phosphate enhances activity of fructose-1,6/sedoheptulose-1,7-bisphosphatase (F/SBPase) from Synechocystis sp. PCC 6803 and Cupriavidus necator in reducing conditions, suggesting a convergent feed-forward activation of the cycle. In oxidizing conditions, glyceraldehyde-3-phosphate inhibits Synechocystis F/SBPase by promoting enzyme aggregation. In contrast, the glycolytic intermediate glucose-6-phosphate activates F/SBPase from Cupriavidus necator but not F/SBPase from Synechocystis. Thus, metabolite-level regulation of the Calvin cycle is more prevalent than previously appreciated.
Keywords:Applied Microbiology, Biochemical Networks, Proteomic Analysis
Source:Communications Biology
ISSN:2399-3642
Publisher:Springer Nature
Volume:6
Number:1
Page Range:947
Date:18 September 2023
Official Publication:https://doi.org/10.1038/s42003-023-05318-8
PubMed:View item in PubMed

Repository Staff Only: item control page

Downloads

Downloads per month over past year

Open Access
MDC Library