2016
DOI: 10.1016/j.ymben.2016.10.002
|View full text |Cite
|
Sign up to set email alerts
|

In silico metabolic engineering of Clostridium ljungdahlii for synthesis gas fermentation

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
16
0

Year Published

2017
2017
2023
2023

Publication Types

Select...
4
3
1

Relationship

1
7

Authors

Journals

citations
Cited by 38 publications
(16 citation statements)
references
References 51 publications
0
16
0
Order By: Relevance
“…In addition, since growth rates estimated by genomescale reconstructions of C. ljungdahlii and C. autoethanogenum [25,37] used the same µ max value reported by [47], their estimations are also comparable with those made by the biothermodynamics-based black-box model (see Additional file 1: Figure S4).…”
Section: Assessment Of Kinetic Parametersmentioning
confidence: 60%
See 1 more Smart Citation
“…In addition, since growth rates estimated by genomescale reconstructions of C. ljungdahlii and C. autoethanogenum [25,37] used the same µ max value reported by [47], their estimations are also comparable with those made by the biothermodynamics-based black-box model (see Additional file 1: Figure S4).…”
Section: Assessment Of Kinetic Parametersmentioning
confidence: 60%
“…Several types of mathematical models have been proposed for understanding and predicting the behavior of microorganisms in gas fermentations [21][22][23][24][25][26][27]; other simpler models have been used for estimating process performance [4,5,[28][29][30][31]. The most popular of the modeling strategies employed recently by researchers is the genome-scale modeling (GSM), which has been used for assessing several features of the intracellular processes in C. ljungdahlii and C. autoethanogenum during syngas fermentations, e.g, the influence of the link between energy conservation and carbon metabolism on the selectivity between ethanol and acetic acid [25,[32][33][34], the co-factor specificity of certain enzymes linked to energy conservation [32,33,35], the formation of biofilms [26], the possibility of boosting ATP production by supplying arginine [36], and the feasibility of gene knock-out to reach overproduction of native and non-native products of acetogens [37]. Alternatively, with issues generally regarding on the accuracy of the quantitative predictions, GSM has also been used to assess the behavior of simulated microorganism inside large-scale bioreactors [21,26,37,38]; the main cause for these latter issues may be credited to the interlinking between the intracellular processes and the environmental conditions given by the bioreactor, besides GSM's large dependency on the objective function and the constraints applied to solve the intracellular rates of reaction [25].…”
Section: Introductionmentioning
confidence: 99%
“…By contrast, 2,3‐butanediol was produced in appreciable amounts only with the recycle reactors, which was attributable to higher volumetric CO consumption rates across the column compared with the conventional reactors. Further increases in 2,3‐butanediol production could be achieved in silico by modifying the C. autoethanogenum reconstruction according to published metabolic engineering strategies (Chen & Henson, ). The conventional reactors produced higher dissolved CO concentrations (Figure b) due to reduced reaction rate, lower CO conversions and higher CO concentrations in the gas phase.…”
Section: Resultsmentioning
confidence: 99%
“…Moreover, genome-scale metabolic flux balance analysis has been used to construct spatiotemporal metabolic models for Clostridium ljungdahlii [131]. When combined with the Optknock computation, the models could predict new gene knockout targets relevant to the overproduction of ethanol, lactate and 2,3-BDO in a bubble column reactor [132]. …”
Section: Use Of Omics Based Technology To Monitor Bioprocess Performancementioning
confidence: 99%