Metabolic engineering of ketocarotenoid formation in higher plants

被引:135
作者
Ralley, L
Enfissi, EMA
Misawa, N
Schuch, W
Bramley, PM
Fraser, PD [1 ]
机构
[1] Univ London, Sch Biol Sci, Egham TW20 0EX, Surrey, England
[2] Marine Biotechnol Inst, Heita, Kamashi 0260001, Japan
[3] Cellfor Inc, Vancouver, BC V6C 268, Canada
关键词
metabolic engineering; carotenoids; multi-gene construct; metabolite profiling; oxygenase; hydroxylase;
D O I
10.1111/j.1365-313X.2004.02151.x
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Although higher plants synthesize carotenoids, they do not possess the ability to form ketocarotenoids. In order to generate higher plants capable of synthesizing combinations of ketolated and hydroxylated carotenoids the genes responsible for the carotene 4,4' oxygenase and 3,3' hydroxylase have been transformed into tomato and tobacco. The gene products were produced as a polyprotein. Subsequent cleavage of the polyprotein, targeting of the two enzymes to the plastid and enzyme activities have been shown for both gene products. Metabolite profiling has shown the formation of ketolated carotenoids from beta-carotene and its hydroxylated intermediates in tobacco and tomato leaf. In the nectary tissues of tobacco flowers a quantitative increase (10-fold) as well as compositional changes were evident, including the presence of astaxanthin, canthaxanthin and 4-ketozeaxanthin. Interestingly, in this tissue the newly formed carotenoids resided predominantly as esters. These data are discussed in terms of metabolic engineering of carotenoids and their sequestration in higher plant tissues.
引用
收藏
页码:477 / 486
页数:10
相关论文
共 38 条
[21]   Metabolic engineering of astaxanthin production in tobacco flowers [J].
Mann, V ;
Harker, M ;
Pecker, I ;
Hirschberg, J .
NATURE BIOTECHNOLOGY, 2000, 18 (08) :888-892
[22]  
MERZ U, 2000, BUSINESS REPORT GLOB
[23]   EXPRESSION OF AN ERWINIA PHYTOENE DESATURASE GENE NOT ONLY CONFERS MULTIPLE RESISTANCE TO HERBICIDES INTERFERING WITH CAROTENOID BIOSYNTHESIS BUT ALSO ALTERS XANTHOPHYLL METABOLISM IN TRANSGENIC PLANTS [J].
MISAWA, N ;
MASAMOTO, K ;
HORI, T ;
OHTANI, T ;
BOGER, P ;
SANDMANN, G .
PLANT JOURNAL, 1994, 6 (04) :481-489
[24]   STRUCTURE AND FUNCTIONAL-ANALYSIS OF A MARINE BACTERIAL CAROTENOID BIOSYNTHESIS GENE-CLUSTER AND ASTAXANTHIN BIOSYNTHETIC-PATHWAY PROPOSED AT THE GENE LEVEL [J].
MISAWA, N ;
SATOMI, Y ;
KONDO, K ;
YOKOYAMA, A ;
KAJIWARA, S ;
SAITO, T ;
OHTANI, T ;
MIKI, W .
JOURNAL OF BACTERIOLOGY, 1995, 177 (22) :6575-6584
[25]  
Miura Y, 1998, APPL ENVIRON MICROB, V64, P1226
[26]   ASTAXANTHIN AND CANTHAXANTHIN ARE POTENT ANTIOXIDANTS IN A MEMBRANE MODEL [J].
PALOZZA, P ;
KRINSKY, NI .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1992, 297 (02) :291-295
[27]   Lutein and lutein ester content in different types of Tagetes patula and T-erecta [J].
Piccaglia, R ;
Marotti, M ;
Grandi, S .
INDUSTRIAL CROPS AND PRODUCTS, 1998, 8 (01) :45-51
[28]   Coordinate expression of multiple bacterial carotenoid genes in canola leading to altered carotenoid production [J].
Ravanello, MP ;
Ke, DY ;
Alvarez, J ;
Huang, BH ;
Shewmaker, CK .
METABOLIC ENGINEERING, 2003, 5 (04) :255-263
[29]   NATURAL OCCURRENCE OF ENANTIOMETRIC AND MESO-ASTAXANTHIN .3. OPTICAL PURITY OF (3S,3'S)-ASTAXANTHIN FROM HAEMATOCOCCUS-PLUVIALIS [J].
RENSTROM, B ;
BORCH, G ;
SKULBERG, OM ;
LIAAENJENSEN, S .
PHYTOCHEMISTRY, 1981, 20 (11) :2561-2564
[30]   Elevation of the provitamin A content of transgenic tomato plants [J].
Römer, S ;
Fraser, PD ;
Kiano, JW ;
Shipton, CA ;
Misawa, N ;
Schuch, W ;
Bramley, PM .
NATURE BIOTECHNOLOGY, 2000, 18 (06) :666-669