Transgenic potato plants expressing human CYP1A1 and human CYP1Al/yeast NAD
PH-cytochrome P450 reductase (YR) fused enzyme were generated from microtub
ers by the use of an Agrobacterium transformation system. The transgenic pl
ants S1384 expressing human CYP1A1 and both F1386 and F1515 expressing the
fused enzyme were selected by kanamycin resistance, PCR analysis, chlortolu
ron (CT) resistance, and Western blot analysis. The integration and transcr
iption of the corresponding CYP1A1 genes were confirmed in these selected t
ransgenic plants by Southern and Northern blot analyses. CYP1A1 and its fus
ed proteins were found to be produced in the transgenic plants S1384 and F1
515, respectively. The P450-dependent monooxygenase activity of the transge
nic plants S1384, S1386, and F1515 was 3.5, 4.2, and 3.8 times higher in 7-
ethoxycoumarin O-deethylation in vitro and 6.4, 5.8, and 5.3 times higher i
n [C-14]CT metabolism in viva than those of the control plants, respectivel
y. In the metabolism of [C-14]atrazine (AT), four metabolites were found in
both control and transgenic plants. The deisopropylated deethylated metabo
lite DIDE, which is nonphytotoxic, was produced to a higher extent in S1384
and F1515 compared with the control. With herbicide tolerance tests, S1384
showed tolerance toward both AT and pyriminobacmethyl (PM), and F1386 and
F1515 were tolerant toward PM, while the control died by treatment with bot
h herbicides. Thus, it was found that the transgenic potato plants expressi
ng human CYP1A1 metabolized the herbicides CT and AT with different structu
res and herbicide modes of action and resulted in cross-tolerance to both h
erbicides as well as PM. (C) 1999 Academic Press.