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Expression of a Pseudomonas aeruginosa Citrate Synthase Gene in Tobacco Is Not Associated with Either Enhanced Citrate Accumulation or Efflux

机译:铜绿假单胞菌柠檬酸盐的表达 烟草中的合成酶基因与柠檬酸盐含量均不相关 积累或外流

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摘要

Aluminum (Al) toxicity and poor phosphorus (P) availability are factors that limit plant growth on many agricultural soils. Previous work reported that expression of a Pseudomonas aeruginosa citrate synthase gene in tobacco (Nicotiana tabacum; CSb lines) resulted in improved Al tolerance (J.M. de la Fuente, V. Ramírez-Rodríguez, J.L. Cabrera-Ponce, L. Herrera-Estrella [1997] Science 276: 1566–1568) and an enhanced ability to acquire P from alkaline soils (J. López-Bucio, O. Martínez de la Vega, A. Guevara-García, L. Herrera-Estrella [2000] Nat Biotechnol 18: 450–453). These effects were attributed to the P. aeruginosa citrate synthase increasing the biosynthesis and efflux of citrate from roots. To verify these findings we: (a) characterized citrate efflux from roots of wild-type tobacco; (b) generated tobacco lines expressing the citrate synthase gene from P. aeruginosa; and (c) analyzed selected CSb lines described above. Al stimulated citrate efflux from intact roots of wild-type tobacco and root apices were found to be responsible for most of the efflux. Despite generating transgenic tobacco lines that expressed the citrate synthase protein at up to a 100-fold greater level than the previously described CSb lines, these lines did not show increased accumulation of citrate in roots or increased Al-activated efflux of citrate from roots. Selected CSb lines, similarly, failed to show differences compared with controls in either citrate accumulation or efflux. We conclude that expression of the P. aeruginosa citrate synthase gene in plants is unlikely to be a robust and easily reproducible strategy for enhancing the Al tolerance and P-nutrition of crop and pasture species.
机译:铝(Al)的毒性和磷(P)的利用率差是限制许多农业土壤上植物生长的因素。先前的工作报道,在烟草中(烟草(Nicotiana tabacum; CSb品系)表达铜绿假单胞菌柠檬酸合酶基因可提高铝的耐受性(JM de la Fuente,V。Ramírez-Rodríguez,JL Cabrera-Ponce,L。Herrera-Estrella [1997] ] Science 276:1566-1568)和从碱性土壤中获取P的能力得到增强(J.López-Bucio,O。Martínezde la Vega,A。Guevara-García,L。Herrera-Estrella [2000] Nat Biotechnol 18: 450–453)。这些作用归因于铜绿假单胞菌柠檬酸合酶增加了柠檬酸根的生物合成和外排。为了验证这些发现,我们:(a)表征了野生型烟草根部的柠檬酸盐外流; (b)产生表达铜绿假单胞菌柠檬酸合酶基因的烟草品系; (c)分析了上述选择的CSb线。铝刺激的野生型烟草完整根和根尖的柠檬酸外排是 负责大部分外排。尽管产生了转基因 表达柠檬酸合酶蛋白的烟草品系高达 这些水平比之前描述的CSb线高100倍 品系没有显示柠檬酸盐在根或 增加了铝激活的柠檬酸根。选定的CSb 类似地,与 柠檬酸盐蓄积或流出。我们得出结论, 植物中的铜绿假单胞菌柠檬酸合酶基因是 不可能是一个健壮且易于复制的增强策略 作物和牧草品种的耐铝性和磷营养。

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