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去除氧化还原敏感的 Rubisco 激活酶不会改变大豆中 Rubisco 的调节。

Removal of redox-sensitive Rubisco Activase does not alter Rubisco regulation in soybean.

机构信息

Agricultural Research Service, Global Change and Photosynthesis Research Unit, United States Department of Agriculture, Urbana, IL, USA.

Carl R. Woese Institute for Genomic Biology, University of Illinois at Urbana-Champaign, Urbana, IL, USA.

出版信息

Photosynth Res. 2022 Nov;154(2):169-182. doi: 10.1007/s11120-022-00962-3. Epub 2022 Sep 27.

Abstract

Rubisco activase (Rca) facilitates the catalytic repair of Rubisco, the CO-fixing enzyme of photosynthesis, following periods of darkness, low to high light transitions or stress. Removal of the redox-regulated isoform of Rubisco activase, Rca-α, enhances photosynthetic induction in Arabidopsis and has been suggested as a strategy for the improvement of crops, which may experience frequent light transitions in the field; however, this has never been tested in a crop species. Therefore, we used RNAi to reduce the Rca-α content of soybean (Glycine max cv. Williams 82) below detectable levels and then characterized the growth, photosynthesis, and Rubisco activity of the resulting transgenics, in both growth chamber and field conditions. Under a 16 h sine wave photoperiod, the reduction of Rca-α contents had no impact on morphological characteristics, leaf expansion rate, or total biomass. Photosynthetic induction rates were unaltered in both chamber-grown and field-grown plants. Plants with reduced Rca-α content maintained the ability to regulate Rubisco activity in low light just as in control plants. This result suggests that in soybean, Rca-α is not as centrally involved in the regulation of Rca oligomer activity as it is in Arabidopsis. The isoform stoichiometry supports this conclusion, as Rca-α comprises only ~ 10% of the Rubisco activase content of soybean, compared to ~ 50% in Arabidopsis. This is likely to hold true in other species that contain a low ratio of Rca-α to Rca-ß isoforms.

摘要

核酮糖-1,5-二磷酸羧化酶加氧酶激活酶(Rca)可促进光合作用 CO2 固定酶核酮糖-1,5-二磷酸羧化酶(Rubisco)在黑暗、高光到低光转换或胁迫期后的催化修复。去除 Rubisco 激活酶的氧化还原调节同工型 Rca-α,可增强拟南芥的光合作用诱导,并且已被提议作为提高作物的策略,这些作物可能在田间经历频繁的光转换;然而,这从未在作物物种中进行过测试。因此,我们使用 RNAi 将大豆(Glycine max cv. Williams 82)中的 Rca-α 含量降低到检测水平以下,然后在生长室和田间条件下对由此产生的转基因植物的生长、光合作用和 Rubisco 活性进行了表征。在 16 h 正弦光周期下,Rca-α 含量的降低对形态特征、叶片扩展率或总生物量没有影响。在生长室和田间生长的植物中,光合作用诱导率没有改变。Rca-α 含量降低的植物与对照植物一样,仍然能够在低光照下调节 Rubisco 活性。这一结果表明,在大豆中,Rca-α 不像在拟南芥中那样,在调节 Rca 寡聚物活性方面起核心作用。同工型的比例支持了这一结论,因为与拟南芥相比,Rca-α 仅占大豆 Rubisco 激活酶含量的10%,而在拟南芥中占50%。这很可能适用于其他含有低比例 Rca-α 和 Rca-ß 同工型的物种。

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