Simulating cyanobacterial phenotypes by integrating flux balance analysis, kinetics, and a light distribution function. Issue 1 (December 2015)
- Record Type:
- Journal Article
- Title:
- Simulating cyanobacterial phenotypes by integrating flux balance analysis, kinetics, and a light distribution function. Issue 1 (December 2015)
- Main Title:
- Simulating cyanobacterial phenotypes by integrating flux balance analysis, kinetics, and a light distribution function
- Authors:
- He, Lian
Wu, Stephen
Wan, Ni
Reding, Adrienne
Tang, Yinjie - Abstract:
- Abstract Background Genome-scale models (GSMs) are widely used to predict cyanobacterial phenotypes in photobioreactors (PBRs). However, stoichiometric GSMs mainly focus on fluxome that result in maximal yields. Cyanobacterial metabolism is controlled by both intracellular enzymes and photobioreactor conditions. To connect both intracellular and extracellular information and achieve a better understanding of PBRs productivities, this study integrates a genome-scale metabolic model ofSynechocystis 6803 with growth kinetics, cell movements, and a light distribution function. The hybrid platform not only maps flux dynamics in cells of sub-populations but also predicts overall production titer and rate in PBRs. Results Analysis of the integrated GSM demonstrates several results. First, cyanobacteria are capable of reaching high biomass concentration (>20 g/L in 21 days) in PBRs without light and CO2 mass transfer limitations. Second, fluxome in a single cyanobacterium may show stochastic changes due to random cell movements in PBRs. Third, insufficient light due to cell self-shading can activate the oxidative pentose phosphate pathway in subpopulation cells. Fourth, the model indicates that the removal of glycogen synthesis pathway may not improve cyanobacterial bio-production in large-size PBRs, because glycogen can support cell growth in the dark zones. Based on experimental data, the integrated GSM estimates thatSynechocystis 6803 in shake flask conditions has aAbstract Background Genome-scale models (GSMs) are widely used to predict cyanobacterial phenotypes in photobioreactors (PBRs). However, stoichiometric GSMs mainly focus on fluxome that result in maximal yields. Cyanobacterial metabolism is controlled by both intracellular enzymes and photobioreactor conditions. To connect both intracellular and extracellular information and achieve a better understanding of PBRs productivities, this study integrates a genome-scale metabolic model ofSynechocystis 6803 with growth kinetics, cell movements, and a light distribution function. The hybrid platform not only maps flux dynamics in cells of sub-populations but also predicts overall production titer and rate in PBRs. Results Analysis of the integrated GSM demonstrates several results. First, cyanobacteria are capable of reaching high biomass concentration (>20 g/L in 21 days) in PBRs without light and CO2 mass transfer limitations. Second, fluxome in a single cyanobacterium may show stochastic changes due to random cell movements in PBRs. Third, insufficient light due to cell self-shading can activate the oxidative pentose phosphate pathway in subpopulation cells. Fourth, the model indicates that the removal of glycogen synthesis pathway may not improve cyanobacterial bio-production in large-size PBRs, because glycogen can support cell growth in the dark zones. Based on experimental data, the integrated GSM estimates thatSynechocystis 6803 in shake flask conditions has a photosynthesis efficiency of ~2.7 %. Conclusions The multiple-scale integrated GSM, which examines both intracellular and extracellular domains, can be used to predict production yield/rate/titer in large-size PBRs. More importantly, genetic engineering strategies predicted by a traditional GSM may work well only in optimal growth conditions. In contrast, the integrated GSM may reveal mutant physiologies in diverse bioreactor conditions, leading to the design of robust strains with high chances of success in industrial settings. … (more)
- Is Part Of:
- Microbial cell factories. Volume 14:Issue 1(2015)
- Journal:
- Microbial cell factories
- Issue:
- Volume 14:Issue 1(2015)
- Issue Display:
- Volume 14, Issue 1 (2015)
- Year:
- 2015
- Volume:
- 14
- Issue:
- 1
- Issue Sort Value:
- 2015-0014-0001-0000
- Page Start:
- 1
- Page End:
- 11
- Publication Date:
- 2015-12
- Subjects:
- Glycogen -- Multiple-scale modeling -- Photobioreactors -- Photosynthesis efficiency -- Self-shading -- Synechocystis 6803
Microbial biotechnology -- Periodicals
Recombinant proteins -- Synthesis -- Periodicals
660.62 - Journal URLs:
- http://pubmedcentral.nih.gov/tocrender.fcgi?journal=100 ↗
http://www.biomedcentral.com/1475-2859 ↗
http://www.microbialcellfactories.com/ ↗
http://link.springer.com/ ↗ - DOI:
- 10.1186/s12934-015-0396-0 ↗
- Languages:
- English
- ISSNs:
- 1475-2859
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 9998.xml