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Appl. Environ. Microbiol., Jun 1997, 2366-2371, Vol 63, No. 6
L Olsson, ME Larsen, B Ronnow, JD Mikkelsen and J Nielsen
Silencing of MIG1, a transcription factor imposing carbon catabolite
repression on invertase, was attempted, either by disrupting the gene or by
expressing antisense copies of the gene. The performance of the recombinant
strains in bioreactor batch cultivations on sucrose, in the presence of
glucose, was compared with that of the wild-type strain under the same
conditions. In the delta migI strain, the rate of sucrose utilization was
independent (10 mmol/g/h) of the glucose concentration. During the
cultivations with the wild-type strain and the antisense strains, two
distinct phases were observed. The rates of sucrose hydrolysis were < 1
mmol/g/h and 9 to 10 mmol/g/h in the first and second phases, respectively.
Entry into the second cultivation phase was characterized by a decline in
glucose concentration below 12 mmol/liter. As expected, disruption of MIG1
resulted in a relief of glucose repression. However, silencing of MIG1
expression was not achieved by expressing antisense MIG1, even though
antisense MIG1 RNA was sufficiently stable to be detected. In the wild-type
and delta migI strains, the specific growth rate was 0.32 to 0.33 h-1,
whereas it was lower in the antisense strains, 0.25 to 0.30 h-1.
Copyright © 1997, American Society for Microbiology
Silencing MIG1 in Saccharomyces cerevisiae: effects of antisense MIG1 expression and MIG1 gene disruption
Department of Biotechnology, Technical University of Denmark, Lyngby, Denmark.
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