» Articles » PMID: 27602057

Exploring Complex Cellular Phenotypes and Model-guided Strain Design with a Novel Genome-scale Metabolic Model of Clostridium Thermocellum DSM 1313 Implementing an Adjustable Cellulosome

Overview
Publisher Biomed Central
Specialty Biotechnology
Date 2016 Sep 8
PMID 27602057
Citations 11
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Clostridium thermocellum is a gram-positive thermophile that can directly convert lignocellulosic material into biofuels. The metabolism of C. thermocellum contains many branches and redundancies which limit biofuel production, and typical genetic techniques are time-consuming. Further, the genome sequence of a genetically tractable strain C. thermocellum DSM 1313 has been recently sequenced and annotated. Therefore, developing a comprehensive, predictive, genome-scale metabolic model of DSM 1313 is desired for elucidating its complex phenotypes and facilitating model-guided metabolic engineering.

Results: We constructed a genome-scale metabolic model iAT601 for DSM 1313 using the KEGG database as a scaffold and an extensive literature review and bioinformatic analysis for model refinement. Next, we used several sets of experimental data to train the model, e.g., estimation of the ATP requirement for growth-associated maintenance (13.5 mmol ATP/g DCW/h) and cellulosome synthesis (57 mmol ATP/g cellulosome/h). Using our tuned model, we investigated the effect of cellodextrin lengths on cell yields, and could predict in silico experimentally observed differences in cell yield based on which cellodextrin species is assimilated. We further employed our tuned model to analyze the experimentally observed differences in fermentation profiles (i.e., the ethanol to acetate ratio) between cellobiose- and cellulose-grown cultures and infer regulatory mechanisms to explain the phenotypic differences. Finally, we used the model to design over 250 genetic modification strategies with the potential to optimize ethanol production, 6155 for hydrogen production, and 28 for isobutanol production.

Conclusions: Our developed genome-scale model iAT601 is capable of accurately predicting complex cellular phenotypes under a variety of conditions and serves as a high-quality platform for model-guided strain design and metabolic engineering to produce industrial biofuels and chemicals of interest.

Citing Articles

The Roles of Nicotinamide Adenine Dinucleotide Phosphate Reoxidation and Ammonium Assimilation in the Secretion of Amino Acids as Byproducts of Clostridium thermocellum.

Yayo J, Rydzak T, Kuil T, Karlsson A, Harding D, Guss A Appl Environ Microbiol. 2023; 89(1):e0175322.

PMID: 36625594 PMC: 9888227. DOI: 10.1128/aem.01753-22.


Genome-scale reconstruction and metabolic modelling of the fast-growing thermophile sp. LC300.

Ljungqvist E, Gustavsson M Metab Eng Commun. 2022; 15:e00212.

PMID: 36425956 PMC: 9678985. DOI: 10.1016/j.mec.2022.e00212.


Model-based driving mechanism analysis for butyric acid production in Clostridium tyrobutyricum.

Feng J, Guo X, Cai F, Fu H, Wang J Biotechnol Biofuels Bioprod. 2022; 15(1):71.

PMID: 35752796 PMC: 9233315. DOI: 10.1186/s13068-022-02169-z.


Functional Analysis of H-Pumping Membrane-Bound Pyrophosphatase, ADP-Glucose Synthase, and Pyruvate Phosphate Dikinase as Pyrophosphate Sources in Clostridium thermocellum.

Kuil T, Hon S, Yayo J, Foster C, Ravagnan G, Maranas C Appl Environ Microbiol. 2021; 88(4):e0185721.

PMID: 34936842 PMC: 8863071. DOI: 10.1128/AEM.01857-21.


Development of a Genome-Scale Metabolic Model of and Its Applications for Integration of Multi-Omics Datasets and Computational Strain Design.

Garcia S, Thompson R, Giannone R, Dash S, Maranas C, Trinh C Front Bioeng Biotechnol. 2020; 8:772.

PMID: 32974289 PMC: 7471609. DOI: 10.3389/fbioe.2020.00772.


References
1.
McAnulty M, Yen J, Freedman B, Senger R . Genome-scale modeling using flux ratio constraints to enable metabolic engineering of clostridial metabolism in silico. BMC Syst Biol. 2012; 6:42. PMC: 3495714. DOI: 10.1186/1752-0509-6-42. View

2.
Bernard T, Bridge A, Morgat A, Moretti S, Xenarios I, Pagni M . Reconciliation of metabolites and biochemical reactions for metabolic networks. Brief Bioinform. 2012; 15(1):123-35. PMC: 3896926. DOI: 10.1093/bib/bbs058. View

3.
von Kamp A, Klamt S . Enumeration of smallest intervention strategies in genome-scale metabolic networks. PLoS Comput Biol. 2014; 10(1):e1003378. PMC: 3879096. DOI: 10.1371/journal.pcbi.1003378. View

4.
Chung B, Lee D . Flux-sum analysis: a metabolite-centric approach for understanding the metabolic network. BMC Syst Biol. 2009; 3:117. PMC: 2805632. DOI: 10.1186/1752-0509-3-117. View

5.
Kridelbaugh D, Nelson J, Engle N, Tschaplinski T, Graham D . Nitrogen and sulfur requirements for Clostridium thermocellum and Caldicellulosiruptor bescii on cellulosic substrates in minimal nutrient media. Bioresour Technol. 2013; 130:125-35. DOI: 10.1016/j.biortech.2012.12.006. View