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@ARTICLE{Curves:34117,
author = {Curves, S. and Linnemann, J. and Klauser, T. and Wandrey,
C. and Takors, R.},
title = {{R}ecombinant protein production with pichia pastoris in
continuous fermentation - kinetic analysis of growth and
production formation},
journal = {Chemie - Ingenieur - Technik},
volume = {73},
issn = {0009-286X},
address = {Weinheim},
publisher = {Wiley-VCH Verl.},
reportid = {PreJuSER-34117},
pages = {1615 - 1621},
year = {2001},
note = {Record converted from VDB: 12.11.2012},
abstract = {Continuous fermentation was applied to the production of
recombinant human chymotrypsinogen B (hCTRB) by the
methylotrophic yeast Pichia pastoris as a tool for the
kinetic analysis of growth and product formation. Using
methanol as the sole source of carbon, energy, and
induction, cell growth could be described by a
non-competitive M ON approach. The maximum growth rate p a,,
was determined to be 0.084 h(-1) and the K-M-value for
methanol to 0.22 g L-1, respectively. With respect to
product formation a similar model was established exhibiting
a methanol concentration of 0.13 g L-1 as the K-M-value and
a maximum biomass-specific product-formation rate Of pi(max)
= 0.23 mg g(-1) h(-1). The production of hCTRB was strictly
growth-coupled.The data provided covers the range of
methanol concentrations between 0 and 4 g L-1. Substrate
concentrations exceeding this upper value led to a complete
collapse of product formation. This change in phenotype
turned out to be irreversible indicating a genetic
instability of transformed Pichia pastoris caused by excess
methanol.},
keywords = {J (WoSType)},
cin = {IBT-2},
ddc = {540},
cid = {I:(DE-Juel1)VDB56},
pnm = {Verfahrenstechnik zur mikrobiellen Gewinnung von
Primärmetaboliten},
pid = {G:(DE-Juel1)FUEK93},
shelfmark = {Engineering, Chemical},
typ = {PUB:(DE-HGF)16},
UT = {WOS:000173288200018},
doi = {10.1002/1522-2640(200112)73:12<1615::AID-CITE1615>3.0.CO;2-6},
url = {https://juser.fz-juelich.de/record/34117},
}