Saponins are bioactive compounds generally considered to be produced by plants to counteract pathogens and herbivores. Besides their role in plant defense, saponins are of growing interest for drug research as they are active constituents of several folk medicines and provide valuable pharmacological properties. Accordingly, much effort has been put into unraveling the modes of action of saponins, as well as in exploration of their potential for industrial processes and pharmacology. However, the exploitation of saponins for bioengineering crop plants with improved resistances against pests as well as circumvention of laborious and uneconomical extraction procedures for industrial production from plants is hampered by the lack of knowledge and availability of genes in saponin biosynthesis. Although the ability to produce saponins is rather widespread among plants, a complete synthetic pathway has not been elucidated in any single species. Current conceptions consider saponins to be derived from intermediates of the phytosterol pathway, and predominantly enzymes belonging to the multigene families of oxidosqualene cyclases (OSCs), cytochromes P450 (P450s) and family 1 UDP-glycosyltransferases (UGTs) are thought to be involved in their biosynthesis. Formation of unique structural features involves additional biosynthetical enzymes of diverse phylogenetic background. As an example of this, a serine carboxypeptidase-like acyltransferase (SCPL) was recently found to be involved in synthesis of triterpenoid saponins in oats. However, the total number of identified genes in saponin biosynthesis remains low as the complexity and diversity of these multigene families impede gene discovery based on sequence analysis and phylogeny. This review summarizes current knowledge of triterpenoid saponin biosynthesis in plants, molecular activities, evolutionary aspects and perspectives for further gene discovery. (C) 2011 Elsevier Ltd. All rights reserved.
机构:Mem Sloan Kettering Canc Ctr, Dept Med, Mol Pharmacol & Chem Program, New York, NY 10065 USA
Adams, Michelle M.
Damani, Payal
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Damani, Payal
Perl, Nicholas R.
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Perl, Nicholas R.
Won, Annie
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Won, Annie
Hong, Feng
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Hong, Feng
Livingston, Philip O.
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Mem Sloan Kettering Canc Ctr, Dept Med, Mol Pharmacol & Chem Program, New York, NY 10065 USAMem Sloan Kettering Canc Ctr, Dept Med, Mol Pharmacol & Chem Program, New York, NY 10065 USA
Livingston, Philip O.
Ragupathi, Govind
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Ragupathi, Govind
Gin, David Y.
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机构:Mem Sloan Kettering Canc Ctr, Dept Med, Mol Pharmacol & Chem Program, New York, NY 10065 USA
机构:Mem Sloan Kettering Canc Ctr, Dept Med, Mol Pharmacol & Chem Program, New York, NY 10065 USA
Adams, Michelle M.
Damani, Payal
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机构:Mem Sloan Kettering Canc Ctr, Dept Med, Mol Pharmacol & Chem Program, New York, NY 10065 USA
Damani, Payal
Perl, Nicholas R.
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机构:Mem Sloan Kettering Canc Ctr, Dept Med, Mol Pharmacol & Chem Program, New York, NY 10065 USA
Perl, Nicholas R.
Won, Annie
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机构:Mem Sloan Kettering Canc Ctr, Dept Med, Mol Pharmacol & Chem Program, New York, NY 10065 USA
Won, Annie
Hong, Feng
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机构:Mem Sloan Kettering Canc Ctr, Dept Med, Mol Pharmacol & Chem Program, New York, NY 10065 USA
Hong, Feng
Livingston, Philip O.
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Mem Sloan Kettering Canc Ctr, Dept Med, Mol Pharmacol & Chem Program, New York, NY 10065 USAMem Sloan Kettering Canc Ctr, Dept Med, Mol Pharmacol & Chem Program, New York, NY 10065 USA
Livingston, Philip O.
Ragupathi, Govind
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h-index: 0
机构:Mem Sloan Kettering Canc Ctr, Dept Med, Mol Pharmacol & Chem Program, New York, NY 10065 USA
Ragupathi, Govind
Gin, David Y.
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机构:Mem Sloan Kettering Canc Ctr, Dept Med, Mol Pharmacol & Chem Program, New York, NY 10065 USA