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首页> 外文期刊>Soil Science and Plant Nutrition >Sucrose transporter NtSUT1 confers aluminum tolerance on cultured cells of tobacco (Nicotiana tabacum L.).
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Sucrose transporter NtSUT1 confers aluminum tolerance on cultured cells of tobacco (Nicotiana tabacum L.).

机译:蔗糖转运蛋白NtSUT1赋予烟草(Nicotiana tabacum L.)培养细胞铝耐受性。

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摘要

The role of plasma membrane-localized sucrose transporter (NtSUT1) was investigated using cultured tobacco cell (Nicotiana tabacum L.) line BY-2. The wild type (WT) cells were first transformed with the NtSUT1 gene or its fragments cloned from tobacco cell line SL to form the over-expression (OX) and suppression (RNAi) cell lines, respectively. Using OX and RNAi transgenics, the role of NtSUT1 in growth capacity of actively growing cells and in aluminum (Al)-treated cells was examined. During the logarithmic phase of growth in nutrient medium containing 2,4-dichlorophenoxyacetic acid (2,4-D), both the rate of sucrose uptake measured with radio-tracer and the content of soluble sugars were higher in OX and lower in RNAi cell lines compared to WT. Overall, the content of soluble sugars negatively correlated with the time necessary for doubling mass (fresh weight). When cells were treated without (control) or with Al in a simple medium containing calcium, sucrose and 2-(N-morpholino)ethanesulfonic acid (MES; pH 5.0) for up to 18 h, the expression of NtSUT1 under its native promoter, or under the control of strong constitutive cauliflower mosaic virus (CaMV) 35S promoter, was strongly dependent on the presence of 2,4-D. Thereafter, the cells were preferentially treated in the presence of 2,4-D. During 6 h after a start of the control treatment, sucrose uptake rates were, compared to WT, slightly higher and lower in OX and RNAi lines respectively. The addition of Al reduced the sucrose uptake rates of OX and WT to the level of RNAi line, indicating that Al inhibits sucrose uptake via NtSUT1. During the post-Al culture of control and Al-treated cells in a nutrient medium, sucrose uptake rates were much higher in OX compared to WT and RNAi lines, which closely and positively correlated with the growth capacity of the cells. Judging from the growth capacity of Al-treated cells relative to that of control cells, OX cells were more tolerant to Al than WT and RNAi. In summary, we conclude that over-expression of NtSUT1 confers higher growth capacity in actively growing cells as well as in Al-treated cells.
机译:使用培养的烟草细胞(Nicotiana tabacum L.)品系BY-2研究了质膜定位的蔗糖转运蛋白(NtSUT1)的作用。首先用NtSUT1基因或其从烟草细胞系SL克隆的片段转化野生型(WT)细胞,分别形成过表达(OX)和抑制(RNAi)细胞系。使用OX和RNAi转基因,检查了NtSUT1在活跃生长的细胞和铝(Al)处理的细胞的生长能力中的作用。在含有2,4-二氯苯氧基乙酸(2,4-D)的营养培养基中的对数生长期,用放射性示踪剂测得的蔗糖摄取率和OX中的可溶性糖含量均较高,而RNAi细胞中的可溶性糖含量较低。线相比WT。总体而言,可溶性糖的含量与质量加倍(鲜重)所需的时间呈负相关。当在含有钙,蔗糖和2-(N-吗啉代)乙磺酸(MES; pH 5.0)的简单培养基中不加(对照)或用Al处理细胞长达18小时时,NtSUT1在其天然启动子下的表达,或在强本构花椰菜花叶病毒(CaMV)35S启动子的控制下强烈依赖于2,4-D的存在。此后,在2,4-D存在下优先处理细胞。在开始对照治疗后的6小时内,与WT相比,OX和RNAi系中的蔗糖摄取率分别略高和较低。 Al的添加将OX和WT的蔗糖摄取速率降低至RNAi系水平,表明Al抑制了通过NtSUT1的蔗糖摄取。在营养培养基中的对照细胞和经Al处理的细胞进行Al的后培养过程中,与WT和RNAi系相比,OX中的蔗糖摄取率要高得多,这与细胞的生长能力密切相关且呈正相关。从经铝处理的细胞相对于对照细胞的生长能力来看,OX细胞比WT和RNAi更能耐受Al。总而言之,我们得出的结论是,NtSUT1的过度表达赋予了活跃生长的细胞以及经过Al处理的细胞更高的生长能力。

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