College of Resources and Environment, Northeast Agricultural University, Harbin, Heilongjiang, China.
College of Veterinary Medicine, Northeast Agricultural University, Harbin, Heilongjiang, China.
Ecotoxicol Environ Saf. 2019 Nov 30;184:109624. doi: 10.1016/j.ecoenv.2019.109624. Epub 2019 Sep 2.
In order to explore the response and adaptation mechanisms of photosynthesis of the leaves of mulberry (Morus alba L.) seedlings to saline-alkali stress. Photosynthetic activity, and the response of related proteomics of M. alba seedling leaves under NaCl and NaHCO stress were studied by using chlorophyll fluorescence and gas exchange technique combined with TMT proteomics. The results showed that NaCl stress had no significant effect on photosystem II (PSII) activity in M. alba seedling leaves. In addition, the expressions of proteins of the PSII oxygen-evolving complex (OEE3-1 and PPD4) and the LHCII antenna (CP24 10A, CP26, and CP29) were increased, and the photosystem I (PSI) activity in the leaves of M. alba seedlings was increased, as well as expressions of proteins, such as PsaF, PsaG, PsaH, PsaL, PsaN, and Ycf4. Under NaHCO stress, the activity of PSII and PSI and the expression of their protein complexes and the electron transfer-related proteins significantly decreased. NaCl stress had little effect on RuBP regeneration during dark reaction in the leaves and the expressions of glucose synthesis related proteins and net photosynthetic rate (P) did not decrease significantly. The leaves could adapt to NaCl stress by reducing stomatal conductance (G) and increasing water use efficiency (WUE). Under NaHCO stress, the expression of dark reaction-related proteins was mostly down-regulated, while G was reduced, which indicated that non-stomatal factors can be responsible for inhibition of carbon assimilation.
为了探索桑树(Morus alba L.)幼苗叶片光合作用对盐碱胁迫的响应和适应机制。采用叶绿素荧光和气体交换技术结合 TMT 蛋白质组学研究了 NaCl 和 NaHCO 胁迫下桑树幼苗叶片的光合作用活性及相关蛋白质组的响应。结果表明,NaCl 胁迫对桑树幼苗叶片 PSII 活性无显著影响。此外,PSII 放氧复合体(OEE3-1 和 PPD4)和 LHCII 天线(CP24 10A、CP26 和 CP29)的蛋白表达增加,PS I 活性增强,PsaF、PsaG、PsaH、PsaL、PsaN 和 Ycf4 等蛋白的表达也增加。在 NaHCO 胁迫下,PSII 和 PSI 的活性及其蛋白复合物和电子传递相关蛋白的表达显著降低。NaCl 胁迫对暗反应中 RuBP 再生的影响较小,与葡萄糖合成相关的蛋白表达和净光合速率(P)没有明显下降。叶片可以通过降低气孔导度(G)和增加水分利用效率(WUE)来适应 NaCl 胁迫。在 NaHCO 胁迫下,暗反应相关蛋白的表达大多下调,同时 G 降低,表明非气孔因素可能导致碳同化抑制。