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@ARTICLE{Bartek:11656,
author = {Bartek, T. and Rudolf, C. and Kerßen, U. and Klein, B. and
Blombach, B. and Lang, S. and Eikmanns, B. and Oldiges, M.},
title = {{S}tudies on substrate utilisation in {L}-valine-producing
{C}orynebacterium glutamicum strains deficient in pyruvate
dehydrogenase complex},
journal = {Bioprocess and biosystems engineering},
volume = {33},
issn = {1615-7591},
address = {Berlin},
publisher = {Springer},
reportid = {PreJuSER-11656},
pages = {873 - 883},
year = {2010},
note = {This work was financially supported by the Fachagentur
Nachwachsende Rohstoffe of the BMVEL-Federal Ministry of
Food, Agriculture and Consumer Protection-(grant
04NR003/22000304) and by Evonik Degussa GmbH. The authors
wish to thank Verena Engels from IBT 1 of Forschungszentrum
Julich GmbH as well as Robert Gerstmeir and Andreas Karau
from Evonik Degussa GmbH for fruitful cooperation and the
valuable discussion of results, and Pia Makus for her
assistance in performing the experiments.},
abstract = {The pyruvate dehydrogenase complex was deleted to increase
precursor availability in Corynebacterium glutamicum strains
overproducing L: -valine. The resulting auxotrophy is
treated by adding acetate in addition glucose for growth,
resulting in the puzzling fact of gluconeogenic growth with
strongly reduced glucose uptake in the presence of acetate
in the medium. This result was proven by intracellular
metabolite analysis and labelling experiments. To increase
productivity, the SugR protein involved in negative
regulation of the phosphotransferase system, was
inactivated, resulting in enhanced consumption of glucose.
However, the surplus in substrate uptake was not converted
to L-valine; instead, the formation of up to 289 microM
xylulose was observed for the first time in C. glutamicum.
As an alternative to the genetic engineering solution, a
straightforward process engineering approach is proposed.
Acetate limitation resulted in a more efficient use of
acetate as cosubstrate, shown by an increased biomass yield
Y(X/Ac) and improved L-valine formation.},
keywords = {Corynebacterium: classification / Corynebacterium:
metabolism / Genetic Enhancement: methods / Pyruvate
Dehydrogenase Complex: genetics / Pyruvate Dehydrogenase
Complex: metabolism / Species Specificity / Substrate
Specificity / Valine: biosynthesis / Pyruvate Dehydrogenase
Complex (NLM Chemicals) / Valine (NLM Chemicals) / J
(WoSType)},
cin = {IBT-2},
ddc = {570},
cid = {I:(DE-Juel1)VDB56},
pnm = {Biotechnologie},
pid = {G:(DE-Juel1)FUEK410},
shelfmark = {Biotechnology $\&$ Applied Microbiology / Engineering,
Chemical},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:20204663},
UT = {WOS:000280892700010},
doi = {10.1007/s00449-010-0410-1},
url = {https://juser.fz-juelich.de/record/11656},
}