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   <subfield code="a">Changing trends in biotechnology of secondary metabolism in medicinal and aromatic plants</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Sumit Gandhi, Vidushi Mahajan, Yashbir Bedi]</subfield>
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   <subfield code="a">Main conclusion : Medicinal and aromatic plants are known to produce secondary metabolites that find uses as flavoring agents, fragrances, insecticides, dyes and drugs. Biotechnology offers several choices through which secondary metabolism in medicinal plants can be altered in innovative ways, to overproduce phytochemicals of interest, to reduce the content of toxic compounds or even to produce novel chemicals. Detailed investigation of chromatin organization and microRNAs affecting biosynthesis of secondary metabolites as well as exploring cryptic biosynthetic clusters and synthetic biology options, may provide additional ways to harness this resource. Plant secondary metabolites are a fascinating class of phytochemicals exhibiting immense chemical diversity. Considerable enigma regarding their natural biological functions and the vast array of pharmacological activities, amongst other uses, make secondary metabolites interesting and important candidates for research. Here, we present an update on changing trends in the biotechnological approaches that are used to understand and exploit the secondary metabolism in medicinal and aromatic plants. Bioprocessing in the form of suspension culture, organ culture or transformed hairy roots has been successful in scaling up secondary metabolite production in many cases. Pathway elucidation and metabolic engineering have been useful to get enhanced yield of the metabolite of interest; or, for producing novel metabolites. Heterologous expression of putative plant secondary metabolite biosynthesis genes in a microbe is useful to validate their functions, and in some cases, also, to produce plant metabolites in microbes. Endophytes, the microbes that normally colonize plant tissues, may also produce the phytochemicals produced by the host plant. The review also provides perspectives on future research in the field.</subfield>
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   <subfield code="a">Springer-Verlag Berlin Heidelberg, 2014</subfield>
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   <subfield code="a">Bioprocessing</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Endophyte</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Hairy roots</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Heterologous expression</subfield>
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   <subfield code="a">Metabolic engineering</subfield>
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   <subfield code="a">Suspension culture</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">4CL : 4-Coumaroyl:CoA ligase</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">CHI : Chalcone isomerase</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">CUS : Curcuminoid synthase</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">CYPs : Cytochrome P450 enzymes</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">DMAPP : Dimethylallyl pyrophosphate</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">EST : Expressed sequenced tag</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">IPP : Isopentenyl pyrophosphate</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">mA : Milli ampere (electric current)</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">MAP : Medicinal and aromatic plants</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">MEP : Methylerythritolphosphate pathway</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">MEV : Mevalonate pathway</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">ORF : Open reading frame</subfield>
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   <subfield code="a">PAL : Phenylalanine ammonia-lyase</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">PLR : Pinoresinol/lariciresinol reductase</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">STS : Stilbene synthase</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">T DNA : Transfer deoxyribose nucleic acid</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">TIA : Terpenoid indole alkaloid pathway</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">US-FDA : United States Food and Drug Administration</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">UV : Ultra violet</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">VIGS : Virus induced gene silencing</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Metadata rights reserved</subfield>
   <subfield code="b">Springer special CC-BY-NC licence</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="D">1</subfield>
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   <subfield code="F">NATIONALLICENCE</subfield>
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