Searched for: subject%3A%22chemostat%22
(1 - 6 of 6)
document
Koopman, F.W. (author), de Winde, J.H. (author), Ruijssenaars, H.J. (author), TNO Kwaliteit van Leven (author)
The solvent-tolerant bacterium Pseudomonas putida S12 was engineered to efficiently utilize the C1 compounds methanol and formaldehyde as auxiliary substrate. The hps and phi genes of Bacillus brevis, encoding two key steps of the ribulose monophosphate (RuMP) pathway, were introduced to construct a pathway for the metabolism of the toxic...
article 2009
document
Verhoef, S. (author), Ruijssenaars, H.J. (author), de Bont, J.A.M. (author), Wery, J. (author), TNO Kwaliteit van Leven (author)
Pseudomonas putida strain S12palB1 was constructed that produces p-hydroxybenzoate from renewable carbon sources via the central metabolite l-tyrosine. P. putida S12palB1 was based on the platform strain P. putida S12TPL3, which has an optimised carbon flux towards l-tyrosine. Phenylalanine ammonia lyase (Pal) was introduced for the conversion...
article 2007
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Barbosa, M.J. (author), Zijffers, J.W. (author), Nisworo, A. (author), Vaes, W. (author), van Schoonhoven, J. (author), Wijffels, R.H. (author), TNO Kwaliteit van Leven (author)
Acceleration-stat (A-stat) cultivations in which the dilution rate is continuously changed at a constant acceleration rate, leading to different average light intensities inside the photobioreactor, can supply more information and reduce experimental time compared with chemostat cultivations. The A-stat was used to optimize the biomass and...
article 2005
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Swift, R.J. (author), Karandikar, A. (author), Griffen, A.M. (author), Punt, P.J. (author), van den Hondel, C.A.M.J.J. (author), Robson, G.D. (author), Trinci, A.P.J. (author), Wiebe, M.G. (author), Centraal Instituut voor Voedingsonderzoek TNO (author)
Aspergillus niger B1, a recombinant strain carrying 20 extra copies of the native glucoamylase gene, was grown in glucose-limited chemostat cultures supplemented with various organic nitrogen sources (dilution rate 0.12 ± 0.01 h-1, pH 5.4). In cultures supplemented with L-alanine, L-methionine, casamino acids, or peptone, specific glucoamylase ...
article 2000
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Santerre Henriksen, A.L. (author), Even, S. (author), Müller, C. (author), Punt, P.J. (author), van den Hondel, C.A.M.J.J. (author), Nielsen, J. (author), Centraal Instituut voor Voedingsonderzoek TNO (author)
An Aspergillus niger strain expressing a red-shifted green fluorescent protein (GFP) in the cytoplasm under the control of the glucoamylase promoter (PglaA) was characterized with respect to its physiology and morphology. Although xylose acted as a repressor carbon source during batch cultivations, PglaA-driven GFP expression by the glucoamylase...
article 1999
document
Withers, J.M. (author), Swift, R.J. (author), Wiebe, M.G. (author), Robson, G.D. (author), Punt, P.J. (author), van den Hondel, C.A.M.J.J. (author), Centraal Instituut voor Voedingsonderzoek TNO (author)
When grown on a medium containing 5 g maltodextrin L-1, Aspergillus niger transformant N402[pAB6-10]B1, which has an additional 20 copies of the glucoamylase (glaA) gene, produced 320 ± 8 mg (mean ± S.E.) glucoamylase (GAM) L-1 in batch culture and 373 ± 9 mg GAM L-1 in maltodextrin- limited chemostat culture at a dilution rate of 0.13 h-1....
article 1998
Searched for: subject%3A%22chemostat%22
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