TY - JOUR
T1 - Release of moth pheromone compounds from Nicotiana benthamiana upon transient expression of heterologous biosynthetic genes
AU - Xia, Yi-Han
AU - Ding, Bao-Jian
AU - Dong, Shuang-Lin
AU - Wang, Hong-Lei
AU - Hofvander, Per
AU - Lofstedt, Christer
PY - 2022
Y1 - 2022
N2 - Background Using genetically modified plants as natural dispensers of insect pheromones may eventually become part of a novel strategy for integrated pest management. Results In the present study, we first characterized essential functional genes for sex pheromone biosynthesis in the rice stem borer Chilo suppressalis (Walker) by heterologous expression in Saccharomyces cerevisiae and Nicotiana benthamiana, including two desaturase genes CsupYPAQ and CsupKPSE and a reductase gene CsupFAR2. Subsequently, we co-expressed CsupYPAQ and CsupFAR2 together with the previously characterized moth desaturase Atr increment 11 in N. benthamiana. This resulted in the production of (Z)-11-hexadecenol together with (Z)-11-hexadecenal, the major pheromone component of C. suppressalis. Both compounds were collected from the transformed N. benthamiana headspace volatiles using solid-phase microextraction. We finally added the expression of a yeast acetyltransferase gene ATF1 and could then confirm also (Z)-11-hexadecenyl acetate release from the plant. Conclusions Our results pave the way for stable transformation of plants to be used as biological pheromone sources in different pest control strategies.
AB - Background Using genetically modified plants as natural dispensers of insect pheromones may eventually become part of a novel strategy for integrated pest management. Results In the present study, we first characterized essential functional genes for sex pheromone biosynthesis in the rice stem borer Chilo suppressalis (Walker) by heterologous expression in Saccharomyces cerevisiae and Nicotiana benthamiana, including two desaturase genes CsupYPAQ and CsupKPSE and a reductase gene CsupFAR2. Subsequently, we co-expressed CsupYPAQ and CsupFAR2 together with the previously characterized moth desaturase Atr increment 11 in N. benthamiana. This resulted in the production of (Z)-11-hexadecenol together with (Z)-11-hexadecenal, the major pheromone component of C. suppressalis. Both compounds were collected from the transformed N. benthamiana headspace volatiles using solid-phase microextraction. We finally added the expression of a yeast acetyltransferase gene ATF1 and could then confirm also (Z)-11-hexadecenyl acetate release from the plant. Conclusions Our results pave the way for stable transformation of plants to be used as biological pheromone sources in different pest control strategies.
KW - Functional characterization
KW - Fatty acyl desaturases
KW - Fatty acyl reductase
KW - Alcohol oxidation
KW - Acetyltransferase
KW - Heterologous expression systems
KW - Pheromone-releasing plants
KW - Functional characterization
KW - Fatty acyl desaturases
KW - Fatty acyl reductase
KW - Alcohol oxidation
KW - Acetyltransferase
KW - Heterologous expression systems
KW - Pheromone-releasing plants
UR - https://res.slu.se/id/publ/116776
U2 - 10.1186/s12915-022-01281-8
DO - 10.1186/s12915-022-01281-8
M3 - Journal article
SN - 1741-7007
VL - 20
JO - BMC Biology
JF - BMC Biology
IS - 1
M1 - 80
ER -