Engineering the plant cell factory for secondary metabolite production

被引:0
作者
R. Verpoorte
R. van der Heijden
J. Memelink
机构
[1] Leiden University,Division of Pharmacognosy, Leiden/Amsterdam Center for Drug Research
[2] Leiden University,Institute of Molecular Plant Sciences
来源
Transgenic Research | 2000年 / 9卷
关键词
Plant secondary metabolism; plant cell factory; metabolic engineering;
D O I
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中图分类号
学科分类号
摘要
Plant secondary metabolism is very important for traits such as flower color, flavor of food, and resistance against pests and diseases. Moreover, it is the source of many fine chemicals such as drugs, dyes, flavors, and fragrances. It is thus of interest to be able to engineer the secondary metabolite production of the plant cell factory, e.g. to produce more of a fine chemical, to produce less of a toxic compound, or even to make new compounds, Engineering of plant secondary metabolism is feasible nowadays, but it requires knowledge of the biosynthetic pathways involved. To increase secondary metabolite production different strategies can be followed, such as overcoming rate limiting steps, reducing flux through competitive pathways, reducing catabolism and overexpression of regulatory genes. For this purpose genes of plant origin can be overexpressed, but also microbial genes have been used successfully. Overexpression of plant genes in microorganisms is another approach, which might be of interest for bioconversion of readily available precursors into valuable fine chemicals. Several examples will be given to illustrate these various approaches. The constraints of metabolic engineering of the plant cell factory will also be discussed. Our limited knowledge of secondary metabolite pathways and the genes involved is one of the main bottlenecks.
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页码:323 / 343
页数:20
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[1]  
Artsaenko O(1994)Construction and functional characterization of a single chain FV antibody-binding to the plant hormone abscicic acid J Plant Physiol 144 427-429
[2]  
Weiler EW(1995)Expression of a single-chain FV antibody against abscisic acid creates a wilty phenotype in transgenic tobacco Plant J 8 745-750
[3]  
Muntz K(1994)Quantitative relationship between phenylalanine ammonia lyase levels and phenylpropnaoid accumulation in transgenic tobacco identifies a rate determining step in natural product synthesis Proc Natl Acad Sci USA 91 7608-7612
[4]  
Conrad U(1993)Increased production of serotonin by suspension and root cultures of Transgen Res 2 336-344
[5]  
Artsaenko O(1999) transformed with a tryptophan decarboxylase cDNA clone from Proc Natl Acad Sci USA 26 12929-12935
[6]  
Peisker M(2000)Interactions among enzymes of the Science 287 818-819
[7]  
Zurnieden U(1998) flavonoid bioynthetic pathway Planta 205 414-419
[8]  
Fiedler U(2000)Biosynthesis meets bioinformatics TibTech 18 181-182
[9]  
Weiler EW(1995)Effects of over-expression of strictosidine synthase and tryptophan decarboxylase on alkaloid production by cell cultures of Annu Rev Plant Physiol Mol Biol 46 521-547
[10]  
Muntz K(2000)New insights into our understanding of the regulation and organization of cell factories Curr Opin Biotechnol 11 209-214