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Literature summary for 1.1.1.27 extracted from

  • Novy, V.; Brunner, B.; Mueller, G.; Nidetzky, B.
    Toward homolactic fermentation of glucose and xylose by engineered Saccharomyces cerevisiae harboring a kinetically efficient L-lactate dehydrogenase within pdc1-pdc5 deletion background (2017), Biotechnol. Bioeng., 114, 163-171.
    View publication on PubMed

Cloned(Commentary)

Cloned (Comment) Organism
gene pfldh, recombinant expression in Saccharomyces cerevisiae, the optimized engineered strain is used as host for L-lactic acid fermentation. Strain IBB10B05 incorporates a NADH-dependent pathway for oxidoreductive xylose assimilation within CEN.PK113-7D background and is additionally evolved for accelerated xylose-to-ethanol fermentation. The pfldh gene is placed in strain IBB10B05 at the pdc1 locus under control of the pdc1 promotor, and strain IBB14LA1_5 additionally has the pdc5 gene disrupted resulting in strain IBB14LA1. The Saccharomyces cerevisiae strain originally optimized for xylose-to-ethanol fermentation is useful to implement L-lactic acid production from glucose and xylose Plasmodium falciparum

Organism

Organism UniProt Comment Textmining
Plasmodium falciparum Q27743
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Synonyms

Synonyms Comment Organism
L-lactate dehydrogenase
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Plasmodium falciparum
L-LDH
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Plasmodium falciparum
PfLDH
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Plasmodium falciparum