乌头酸酶
突变体
柠檬酸循环
生物化学
生物
番茄
光合作用
基因
焊剂(冶金)
新陈代谢
酶
化学
植物
有机化学
作者
Fernando Carrari,Adriano Nunes‐Nesi,Yves Gibon,Anna Lytovchenko,Marcelo Loureiro,Lee Sweetlove
出处
期刊:Plant Physiology
[Oxford University Press]
日期:2003-11-01
卷期号:133 (3): 1322-1335
被引量:207
标识
DOI:10.1104/pp.103.026716
摘要
Abstract Wild species tomato (Lycopersicon pennellii) plants bearing a genetic lesion in the gene encoding aconitase (Aco-1; aconitate hydratase EC 4.2.1.3) were characterized at molecular and biochemical levels. The genetic basis of this lesion was revealed by cloning the wild-type and mutant alleles. The mutation resulted in lowered expression of the Aco-1 transcript and lowered levels of both cytosolic and mitochondrial aconitase protein and activity. After in silico analysis, we concluded that in the absence of a recognizable target sequence, the best explanation for the dual location of this protein is inefficient targeting. Biochemical analysis of leaves of the Aco-1 accession suggested that they exhibited a restricted flux through the Krebs cycle and reduced levels of Krebs cycle intermediates but were characterized by elevated adenylate levels and an enhanced rate of CO2 assimilation. Furthermore, the analysis of both steady-state metabolite levels and metabolic fluxes revealed that this accession also exhibited elevated rates of photosynthetic Suc synthesis and a corresponding increase in fruit yield. Therefore, we conclude that the Krebs cycle normally competes with the Suc synthetic pathway for carbon but is not essential for the supply of energy to fuel the operation of this pathway.
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