The tomato carotenoid cleavage dioxygenase 1 genes contribute to the formation of the flavor volatiles β-ionone, pseudoionone, and geranylacetone

被引:384
作者
Simkin, AJ
Schwartz, SH
Auldridge, M
Taylor, MG
Klee, HJ
机构
[1] Univ Florida, Hort Sci Plant Mol & Cellular Biol Program, Gainesville, FL 32611 USA
[2] Michigan State Univ, Dept Energy, Plant Res Lab, E Lansing, MI 48824 USA
[3] Michigan State Univ, Dept Plant Biol, E Lansing, MI 48824 USA
基金
欧盟地平线“2020”;
关键词
fruit; apocarotenoid; taste; transgenic plants; aroma;
D O I
10.1111/j.1365-313X.2004.02263.x
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Volatile terpenoid compounds, potentially derived from carotenoids, are important components of flavor and aroma in many fruits, vegetables and ornamentals. Despite their importance, little is known about the enzymes that generate these volatiles. The tomato genome contains two closely related genes potentially encoding carotenoid cleavage dioxygenases, LeCCD1A and LeCCD1B. A quantitative reverse transcriptase-polymerase chain reaction analysis revealed that one of these two genes, LeCCD1B, is highly expressed in ripening fruit (4 days post-breaker), where it constitutes 0.11% of total RNA. Unlike the related neoxanthin cleavage dioxygenases, import assays using pea chloroplasts showed that the LeCCD1 proteins are not plastid-localized. The biochemical functions of the LeCCD1 proteins were determined by bacterial expression and in vitro assays, where it was shown that they symmetrically cleave multiple carotenoid substrates at the 9,10 (9',10') positions to produce a C-14 dialdehyde and two C-13 cyclohexones that vary depending on the substrate. The potential roles of the LeCCD1 genes in vivo were assessed in transgenic tomato plants constitutively expressing the LeCCD1B gene in reverse orientation. This over-expression of the antisense transcript led to 87-93% reductions in mRNA levels of both LeCCD1A and LeCCD1B in the leaves and fruits of selected lines. Transgenic plants exhibited no obvious morphological alterations. High-performance liquid chromatography analysis showed no significant modification in the carotenoid content of fruit tissue. However, volatile analysis showed a greater than or equal to50% decrease in beta-ionone (a beta-carotene-derived C-13 cyclohexone) and a greater than or equal to60% decrease in geranylacetone (a C-13 acyclic product likely derived from a lycopene precursor) in selected lines, implicating the LeCCD1 genes in the formation of these important flavor volatiles in vivo.
引用
收藏
页码:882 / 892
页数:11
相关论文
共 56 条
[1]   SYNTHESIS OF THE SMALL SUBUNIT OF RIBULOSE-BISPHOSPHATE CARBOXYLASE FROM GENES CLONED INTO PLASMIDS CONTAINING THE SP6 PROMOTER [J].
ANDERSON, S ;
SMITH, SM .
BIOCHEMICAL JOURNAL, 1986, 240 (03) :709-715
[2]   Flavor trivia and tomato aroma: Biochemistry and possible mechanisms for control of important aroma components [J].
Baldwin, EA ;
Scott, JW ;
Shewmaker, CK ;
Schuch, W .
HORTSCIENCE, 2000, 35 (06) :1013-1022
[3]   QUANTITATIVE-ANALYSIS OF FLAVOR PARAMETERS IN 6 FLORIDA TOMATO CULTIVARS (LYCOPERSICON-ESCULENTUM MILL) [J].
BALDWIN, EA ;
NISPEROSCARRIEDO, MO ;
BAKER, R ;
SCOTT, JW .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1991, 39 (06) :1135-1140
[4]  
Bernacchi S, 2001, Nucleic Acids Res, V29, pE62, DOI 10.1093/nar/29.13.e62
[5]  
BLOCK MA, 1983, J BIOL CHEM, V258, P3281
[6]   MAX3/CCD7 is a carotenoid cleavage dioxygenase required for the synthesis of a novel plant signaling molecule [J].
Booker, J ;
Auldridge, M ;
Wills, S ;
McCarty, D ;
Klee, H ;
Leyser, O .
CURRENT BIOLOGY, 2004, 14 (14) :1232-1238
[7]   Biosynthesis of the food and cosmetic plant pigment bixin (annatto) [J].
Bouvier, F ;
Dogbo, O ;
Camara, B .
SCIENCE, 2003, 300 (5628) :2089-2091
[8]   Oxidative remodeling of chromoplast carotenoids:: Identification of the carotenoid dioxygenase CsCCD and CsZCD genes involved in crocus secondary metabolite biogenesis [J].
Bouvier, F ;
Suire, C ;
Mutterer, J ;
Camara, B .
PLANT CELL, 2003, 15 (01) :47-62
[9]   SYNTHESIS AND PLANT-GROWTH INHIBITORY PROPERTIES OF (+/-)-O-METHYLXANTHOXIN [J].
BURDEN, RS ;
TAYLOR, HF ;
DAWSON, GW .
PHYTOCHEMISTRY, 1972, 11 (07) :2295-+
[10]  
BUTTERY RG, 1993, ACS SYM SER, V525, P23