GEMA CABRERA REVUELTA-rekin lankidetzan egindako argitalpenak (10)

2022

  1. Automatable downstream purification of the benzohydroxamic acid D-DIBOA from a biocatalytic synthesis

    New Biotechnology, Vol. 72, pp. 48-57

  2. Metabolomics for the design of new metabolic engineering strategies for improving aerobic succinic acid production in Escherichia coli

    Metabolomics, Vol. 18, Núm. 8

2021

  1. 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

  1. 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

  1. 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

  2. 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

  1. Heterologous expression of the human Phosphoenol Pyruvate Carboxykinase (hPEPCK-M) improves hydrogen and ethanol synthesis in the Escherichia coli dcuD mutant when grown in a glycerol-based medium

    New Biotechnology, Vol. 35, pp. 1-12

2015

  1. 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

  2. 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

  1. 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