Zhou Ying, Yang Zhenming, Xu Yuezi, Sun Haoran, Sun Zhitao, Lin Bao, Sun Wenjing, You Jiangfeng
Laboratory of Soil and Plant Molecular Genetics, College of Plant Science, Jilin University, Changchun, China.
Front Plant Sci. 2018 Jan 10;8:2246. doi: 10.3389/fpls.2017.02246. eCollection 2017.
Malate accumulation has been suggested to balance Al-induced citrate synthesis and efflux in soybean roots. To test this hypothesis, characteristics of Al-induced accumulation and efflux of citrate and malate were compared between two soybean genotypes combining a functional analysis of putatively encode a cytosolic NADP-malic enzyme. Similar amounts of citrate were released, and root elongation was equally inhibited before 8 h of Al treatment of Jiyu 70 and Jiyu 62 cultivars. Jiyu 70 began to secrete more citrate and exhibited higher Al resistance than did Jiyu 62 at 12 h. A sustained increase in internal malate and citrate concentrations was observed in Jiyu 70 at 24 h of Al treatment. However, Jiyu 62 decreased its malate concentration at 12 h and its citrate concentration at 24 h of Al treatment. GmME1 localized to the cytoplast and clustered closely with cytosolic malic enzymes AtME2 and SgME1 and was constitutively expressed in the roots. Al treatment induced higher NADP-malic enzyme activities and expression levels in Jiyu 70 than in Jiyu 62 within 24 h. Compared with wild-type hairy roots, over-expressing in hairy roots (-OE) produced higher expression levels of but did not change the expression patterns of either of the putative citrate transporter genes and or the malate transporter gene , with or without Al treatment. -OE showed a higher internal concentration and external efflux of both citrate and malate at 4 h of Al stress. Lighter hematoxylin staining and lower Al contents in root apices of -OE hairy roots indicated greater Al resistance. Comprehensive experimental results suggest that sustaining Al-induced citrate efflux depends on the malate pool in soybean root apices. encodes a cytosolic malic enzyme that contributes to increased internal malate and citrate concentrations and their external efflux to confer higher Al resistance.
有人提出,苹果酸积累可平衡铝诱导的大豆根中柠檬酸的合成与外排。为验证这一假设,结合对推测编码胞质NADP - 苹果酸酶的功能分析,比较了两个大豆基因型中铝诱导的柠檬酸和苹果酸积累与外排特征。在对吉育70和吉育62品种进行铝处理8小时之前,释放的柠檬酸量相似,根伸长受到同等程度的抑制。在铝处理12小时时,吉育70开始分泌更多的柠檬酸,并且比吉育62表现出更高的耐铝性。在铝处理24小时时,观察到吉育70内部苹果酸和柠檬酸浓度持续增加。然而,在铝处理12小时时,吉育62的苹果酸浓度下降,在铝处理24小时时,其柠檬酸浓度下降。GmME1定位于细胞质体,与胞质苹果酸酶AtME2和SgME1紧密聚集,并在根中组成型表达。在24小时内,铝处理诱导吉育70中NADP - 苹果酸酶活性和表达水平高于吉育62。与野生型毛状根相比,在毛状根中过表达(-OE)产生更高的 表达水平,但在有无铝处理的情况下,均未改变推测的柠檬酸转运蛋白基因 和 或苹果酸转运蛋白基因 的表达模式。-OE在铝胁迫4小时时,柠檬酸和苹果酸的内部浓度和外部外排均较高。-OE毛状根根尖的苏木精染色较浅且铝含量较低,表明其耐铝性更强。综合实验结果表明,维持铝诱导的柠檬酸外排取决于大豆根尖中的苹果酸库。 编码一种胞质苹果酸酶,有助于增加内部苹果酸和柠檬酸浓度及其外部外排,从而赋予更高的耐铝性。