Analysis of alcohol oxidase isozymes in gene-disrupted strains of methylotrophic yeast Pichia methanolica
Citation
T. Nakagawa et al., Analysis of alcohol oxidase isozymes in gene-disrupted strains of methylotrophic yeast Pichia methanolica, J BIOSCI BI, 91(2), 2001, pp. 225-227
Categorie Soggetti
Biotecnology & Applied Microbiology",Microbiology
Journal title
JOURNAL OF BIOSCIENCE AND BIOENGINEERING
SICI code
1389-1723(200102)91:2<225:AOAOII>2.0.ZU;2-7
Abstract
A cell-free extract of methanol-grown Pichia methanolica cells was found to
contain nine alcohol oxidase (AOD) Isozymes by active staining of a native
polyacrylamide electrophoresis gel. Our previous study revealed that AOD i
n P. methanolica was encoded by two genes, MODI and MOD2, and the results o
f an experiment involving Candida boidinii as an expression host suggested
that the AOD isozymes observed in P. methanolica were due to random associa
tion of Mod1p and Mod2p into an active octamer [Nakagawa et al., Yeast, 15,
1223-1230 (1999)]. This study was conducted using P, methanolica MOD1- and
/or MOD2-gene disrupted strains to confirm a previous hypothesis. While the
cell-free extract of the wild-type strain gave nine ladder bands, the mod1
Delta and mod2 Delta strains gave a single active AOD band corresponding t
o the mobilities of Mod2p and Mod1p on a native electrophoresis gel, respec
tively. The cell-free extract of glycerol-grown wild-type cells gave a sing
le band corresponding to Mod1p, showing that only MOD1 is expressed in glyc
erol-grown cells. While the expression of both MOD1 and MOD2 was induced by
methanol, this finding and our previous observations indicated that the ex
pression of MOD1 and MOD2 was controlled by a distinct regulatory mechanism
in P. methanolica.