TY - JOUR
T1 - Comparative macroarray analysis of morphine containing Papaver somniferum and eight morphine free Papaver species identifies an O-methyltransferase involved in benzylisoquinoline biosynthesis
AU - Ziegler, Jörg
AU - Diaz-Chávez, María Luisa
AU - Kramell, Robert
AU - Ammer, Christian
AU - Kutchan, Toni M.
N1 - Funding Information:
Acknowledgements We thank Silvia Wegener for excellent technical assistance. This work was supported by the Deutsche Fors-chungsgemeinschaft, Bonn, the Deutschen Akademischen Austausch Dienst, Bonn and by the Fonds der Chemischen In-dustrie, Frankfurt. María Luisa Diaz-Chávez was supported by CONACYT, Mexico.
PY - 2005/10
Y1 - 2005/10
N2 - Benzylisoquinoline alkaloids constitute a group of about 2,500 structures and are mainly produced by plants of the order Ranunculales. But only the opium poppy, Papaver somniferum, and Papaver setigerum are able to produce morphine. In this study, we started to investigate by gene expression analysis the molecular basis for this exceptional biosynthetic ability. A sequencing project from P. somniferum seedlings was initiated using a method based on the amplified fragment length polymorphism technique that resulted in 849 UniGenes. These cDNAs were analysed on macroarrays for differential expression between morphine-containing P. somniferum plants and eight other Papaver species, which accumulate other benzylisoquinolines instead of morphine. Three cDNAs showing increased expression in P. somniferum compared to all the other Papaver species were identified. Whereas two showed no significant homology to any known protein, one putatively encoded an O-methyltransferase. Analysis of substrate specificity of the heterologously expressed protein and mass spectrometric identification of the enzymatic products identified this protein as S-adenosyl-L-methionine:(R,S)-3′-hydroxy-N-methylcoclaurine 4′-O-methyltransferase (EC 2.1.1.116). Unlike other O-methyltransferases of different positional specificities implicated in benzylisoquinoline metabolism, the enzyme only accepted tetrahydroxylated tetrahydrobenzylisoquinolines as substrates; methylation was tolerated only at the 6-hydroxy position.
AB - Benzylisoquinoline alkaloids constitute a group of about 2,500 structures and are mainly produced by plants of the order Ranunculales. But only the opium poppy, Papaver somniferum, and Papaver setigerum are able to produce morphine. In this study, we started to investigate by gene expression analysis the molecular basis for this exceptional biosynthetic ability. A sequencing project from P. somniferum seedlings was initiated using a method based on the amplified fragment length polymorphism technique that resulted in 849 UniGenes. These cDNAs were analysed on macroarrays for differential expression between morphine-containing P. somniferum plants and eight other Papaver species, which accumulate other benzylisoquinolines instead of morphine. Three cDNAs showing increased expression in P. somniferum compared to all the other Papaver species were identified. Whereas two showed no significant homology to any known protein, one putatively encoded an O-methyltransferase. Analysis of substrate specificity of the heterologously expressed protein and mass spectrometric identification of the enzymatic products identified this protein as S-adenosyl-L-methionine:(R,S)-3′-hydroxy-N-methylcoclaurine 4′-O-methyltransferase (EC 2.1.1.116). Unlike other O-methyltransferases of different positional specificities implicated in benzylisoquinoline metabolism, the enzyme only accepted tetrahydroxylated tetrahydrobenzylisoquinolines as substrates; methylation was tolerated only at the 6-hydroxy position.
KW - (R, S)-3′-hydroxy-N-methylcoclaurine 4′-O-methyltransferase
KW - Alkaloid biosynthesis
KW - Expressed sequence tags
KW - Macroarray
KW - Opium poppy
KW - Papaver somniferum
UR - https://www.scopus.com/pages/publications/26644468125
U2 - 10.1007/s00425-005-1550-4
DO - 10.1007/s00425-005-1550-4
M3 - Article
C2 - 16034588
AN - SCOPUS:26644468125
SN - 0032-0935
VL - 222
SP - 458
EP - 471
JO - Planta
JF - Planta
IS - 3
ER -