TY - CHAP
T1 - Engineering Plant Alkaloid Biosynthetic Pathways
T2 - Progress and Prospects
AU - Kutchan, Toni M.
AU - Frick, Susanne
AU - Weid, Marion
N1 - Funding Information:
Our results reported in this chapter were from research supported by the Deutsche Forschungsgemeinschaft, Bonn and Fonds der Chemischen Industrie, Frankfurt.
PY - 2008
Y1 - 2008
N2 - With the successful application of molecular genetic methods to the plant alkaloid field, we now have sophisticated tools at our disposal to study regulation of enzymatic biosynthesis, as well as determining the cellular and subcellular localization of these enzymes. The availability of ever-increasing numbers of recombinant enzymes has enabled thorough analyses of selected alkaloid biosynthetic enzymes at the biochemical and structural levels. We are just beginning to use this knowledge to metabolically engineer alkaloid metabolism in plants and in in vitro cultures. Multicellular compartmentation of alkaloid pathways must be considered if meaningful metabolic engineering experiments are to be designed; for example, we will need to use promoters that drive transgene expression in the correct cell types. Regulation of these pathways at the gene and enzyme level is complex and there is still much to be learned about metabolite levels, multienzyme complexes, and pathway interconnections, as we systematically overexpress and suppress gene transcription. Today, pathway engineering in plants remains highly variable. When we perturb cellular physiology, metabolite homeostasis and intra- and intercellular partitioning can be affected in unpredictable ways. Predictive metabolic engineering to generate plants with tailored alkaloid profiles for basic research and for commercial production is clearly a challenge for the future.
AB - With the successful application of molecular genetic methods to the plant alkaloid field, we now have sophisticated tools at our disposal to study regulation of enzymatic biosynthesis, as well as determining the cellular and subcellular localization of these enzymes. The availability of ever-increasing numbers of recombinant enzymes has enabled thorough analyses of selected alkaloid biosynthetic enzymes at the biochemical and structural levels. We are just beginning to use this knowledge to metabolically engineer alkaloid metabolism in plants and in in vitro cultures. Multicellular compartmentation of alkaloid pathways must be considered if meaningful metabolic engineering experiments are to be designed; for example, we will need to use promoters that drive transgene expression in the correct cell types. Regulation of these pathways at the gene and enzyme level is complex and there is still much to be learned about metabolite levels, multienzyme complexes, and pathway interconnections, as we systematically overexpress and suppress gene transcription. Today, pathway engineering in plants remains highly variable. When we perturb cellular physiology, metabolite homeostasis and intra- and intercellular partitioning can be affected in unpredictable ways. Predictive metabolic engineering to generate plants with tailored alkaloid profiles for basic research and for commercial production is clearly a challenge for the future.
KW - (R,S)-3′-Hydroxy-N-methylcoclaurine 4′-O-methyltransferase
KW - (R,S)-Coclaurine
KW - (R,S)-Norcoclaurine 6-O-methyltransferase
KW - (R,S)-Reticuline 7-O-methyltransferase
KW - (S)-Canadine synthase
KW - (S)-N-Methylcoclaurine 3′-hydroxylase
KW - (S)-Scoulerine 9-O-methyltransferase
KW - Ajmaline
KW - Berberine
KW - Berberine bridge enzyme
KW - Calistegin
KW - Cocaine
KW - Codeinone reductase
KW - Deacetylvindoline 4-O-acetyltransferase
KW - Desacetoxyvindoline 4-hydroxlyase
KW - Dopamine
KW - Geraniol 10-hydroxylase
KW - Hyoscyamine
KW - Hyoscyamine 6β-hydroxylase
KW - Laudanine
KW - Major latex protein
KW - Morphine
KW - N-Methyltransferase
KW - Polyneuridine aldehyde esterase
KW - Putrescine N-methyltransferase
KW - Salutaridinol 7-O-acetyltransferase
KW - Sanguinarine
KW - Scopolamine
KW - Secologanin synthase
KW - Strictosidine
KW - Strictosidine glucosidase
KW - Strictosidine synthase
KW - Tabersonine 16-hydroxylase
KW - Tropinone reductase I
KW - Tropinone reductase II
KW - Tryptophan decarboxylase
KW - Tyrosine/dopa decarboxylase
KW - Vindoline
KW - Vinorine synthase
UR - http://www.scopus.com/inward/record.url?scp=65249133122&partnerID=8YFLogxK
U2 - 10.1016/S1755-0408(07)01010-7
DO - 10.1016/S1755-0408(07)01010-7
M3 - Chapter
AN - SCOPUS:65249133122
SN - 9780080449722
T3 - Advances in Plant Biochemistry and Molecular Biology
SP - 283
EP - 310
BT - Advances in Plant Biochemistry and Molecular Biology
ER -