JORGE
BOLIVAR PEREZ
Catedrático de Universidad
ANTONIO
VALLE GALLARDO
Profesor Titular de Universidad
Publicaciones en las que colabora con ANTONIO VALLE GALLARDO (19)
2023
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Application of a Microalgal Peptide-Enriched Extract as Media Component in E. coli Culture
ACS Sustainable Chemistry and Engineering, Vol. 11, Núm. 8, pp. 3529-3538
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Metabolomics of Escherichia coli for Disclosing Novel Metabolic Engineering Strategies for Enhancing Hydrogen and Ethanol Production
International Journal of Molecular Sciences, Vol. 24, Núm. 14
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ZNF330/NOA36 interacts with HSPA1 and HSPA8 and modulates cell cycle and proliferation in response to heat shock in HEK293 cells
Biology Direct, Vol. 18, Núm. 1
2022
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Automatable downstream purification of the benzohydroxamic acid D-DIBOA from a biocatalytic synthesis
New Biotechnology, Vol. 72, pp. 48-57
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Metabolomics for the design of new metabolic engineering strategies for improving aerobic succinic acid production in Escherichia coli
Metabolomics, Vol. 18, Núm. 8
2021
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Co-overexpression of the malate dehydrogenase (Mdh) and the malic enzyme A (MaeA) in several Escherichia coli mutant backgrounds increases malate redirection towards hydrogen production
International Journal of Hydrogen Energy, Vol. 46, Núm. 29, pp. 15337-15350
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Escherichia coli Dcu C4-dicarboxylate transporters dependent proton and potassium fluxes and FOF1-ATPase activity during glucose fermentation at pH 7.5
Bioelectrochemistry, Vol. 141
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Escherichia coli, the workhorse cell factory for the production of chemicals
Microbial Cell Factories Engineering for Production of Biomolecules (Elsevier), pp. 115-137
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Escherichia coli, the workhorse cell factory for the production of chemicals
Microbial Cell Factories Engineering for Production of Biomolecules (Academic Press), pp. 115-137
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Identification of enzymatic bottlenecks for the aerobic production of malate from glycerol by the systematic gene overexpression of anaplerotic enzymes in escherichia coli
International Journal of Molecular Sciences, Vol. 22, Núm. 5, pp. 1-17
2020
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Optimization of the biocatalysis for D‐DIBOA synthesis using a quick and sensitive new spectrophotometric quantification method
International Journal of Molecular Sciences, Vol. 21, Núm. 22, pp. 1-15
2019
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Evidence for Escherichia coli DcuD carrier dependent F O F 1 -ATPase activity during fermentation of glycerol
Scientific Reports, Vol. 9, Núm. 1
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A genetically engineered Escherichia coli strain overexpressing the nitroreductase NfsB is capable of producing the herbicide D-DIBOA with 100% molar yield
Microbial Cell Factories, Vol. 18, Núm. 1
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Metabolic engineering for the optimization of hydrogen production in Escherichia coli: A review
Biotechnology Advances, Vol. 37, Núm. 5, pp. 616-633
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Overexpression of the nitroreductase NfsB in an E. coli strain as a whole-cell biocatalyst for the production of chlorinated analogues of the natural herbicide DIBOA
New Biotechnology, Vol. 50, pp. 9-19
2017
2015
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A systematic analysis of TCA Escherichia coli mutants reveals suitable genetic backgrounds for enhanced hydrogen and ethanol production using glycerol as main carbon source
Biotechnology Journal, Vol. 10, Núm. 11, pp. 1750-1761
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Identification of enhanced hydrogen and ethanol Escherichia coli producer strains in a glycerol-based medium by screening in single-knock out mutant collections
Microbial Cell Factories, Vol. 14, Núm. 1
2012
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Study of the role played by NfsA, NfsB nitroreductase and NemA flavin reductase from Escherichia coli in the conversion of ethyl 2-(2′- nitrophenoxy)acetate to 4-hydroxy-(2H)-1,4-benzoxazin-3(4H)-one (D-DIBOA), a benzohydroxamic acid with interesting biological properties
Applied Microbiology and Biotechnology, Vol. 94, Núm. 1, pp. 163-171