Molecular cloning, expression and characterization of tropinone reductase II, an enzyme of the SDR family in Solanum tuberosum (L.)

被引:32
作者
Keiner, R
Kaiser, H
Nakajima, K
Hashimoto, T
Dräger, B
机构
[1] Univ Halle Wittenberg, Inst Pharmazeut Biol, D-06120 Halle An Der Saale, Germany
[2] Nara Inst Sci & Technol, Grad Sch Biol Sci, Nara 6300101, Japan
基金
日本学术振兴会;
关键词
calystegine; expression; potato; SDR enzymes; tropinone; tropinone reductase;
D O I
10.1023/A:1013315110746
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Calystegines are nortropane alkaloids that are found in Solanaceae containing the classical tropane alkaloids hyoscyamine and scopolamine, and in other Solanaceae such as potato, Solanum tuberosum (L.). Calystegines are assumed to derive from the classical tropane alkaloid pathway. We isolated a cDNA from S. tuberosum with high homology to the pseudotropine-forming tropinone reductase (TRII), which presents as the first putative metabolite specific to calystegines. The equivalent amino acid sequence shows typical motifs of a short-chain dehydrogenase (SDR). The recombinant TRII protein expressed in Escherichia coli catalyzes pseudotropine formation from tropinone with a K-m, value, a pH optimum, substrate and co-substrate preferences similar to those reported for the TRII enzymes from other Solanaceae species. The gene is expressed in roots, tubers and aerial parts of potato. The distribution of the TRII transcript in comparison with the calystegine concentrations in the tissues suggests transport of calystegines or their precursors between potato organs.
引用
收藏
页码:299 / 308
页数:10
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