| Literature DB >> 26113639 |
Thilo Winzer1, Marcelo Kern1, Andrew J King1, Tony R Larson1, Roxana I Teodor1, Samantha L Donninger1, Yi Li1, Adam A Dowle2, Jared Cartwright2, Rachel Bates2, David Ashford2, Jerry Thomas2, Carol Walker3, Tim A Bowser3, Ian A Graham1.
Abstract
Morphinan alkaloids from the opium poppy are used for pain relief. The direction of metabolites to morphinan biosynthesis requires isomerization of (S)- to (R)-reticuline. Characterization of high-reticuline poppy mutants revealed a genetic locus, designated STORR [(S)- to (R)-reticuline] that encodes both cytochrome P450 and oxidoreductase modules, the latter belonging to the aldo-keto reductase family. Metabolite analysis of mutant alleles and heterologous expression demonstrate that the P450 module is responsible for the conversion of (S)-reticuline to 1,2-dehydroreticuline, whereas the oxidoreductase module converts 1,2-dehydroreticuline to (R)-reticuline rather than functioning as a P450 redox partner. Proteomic analysis confirmed that these two modules are contained on a single polypeptide in vivo. This modular assembly implies a selection pressure favoring substrate channeling. The fusion protein STORR may enable microbial-based morphinan production.Entities:
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Year: 2015 PMID: 26113639 DOI: 10.1126/science.aab1852
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728