• ISSN 1008-505X
  • CN 11-3996/S
孙志宇, 刘欣悦, 张思威, 马明珠, 白蕊, 刘欢, 易伯涛, 韩晓日, 刘轶飞. 外源钙缓解花生亚低磷光合障碍的机制[J]. 植物营养与肥料学报, 2022, 28(6): 1055-1066. DOI: 10.11674/zwyf.2021514
引用本文: 孙志宇, 刘欣悦, 张思威, 马明珠, 白蕊, 刘欢, 易伯涛, 韩晓日, 刘轶飞. 外源钙缓解花生亚低磷光合障碍的机制[J]. 植物营养与肥料学报, 2022, 28(6): 1055-1066. DOI: 10.11674/zwyf.2021514
SUN Zhi-yu, LIU Xin-yue, ZHANG Si-wei, MA Ming-zhu, BAI Rui, LIU Huan, YI Bo-tao, HAN Xiao-ri, LIU Yi-fei. Exogenous calcium alleviates phosphorus deficiency-induced photosynthetic inhibition in peanut (Arachis hypogaea)[J]. Journal of Plant Nutrition and Fertilizers, 2022, 28(6): 1055-1066. DOI: 10.11674/zwyf.2021514
Citation: SUN Zhi-yu, LIU Xin-yue, ZHANG Si-wei, MA Ming-zhu, BAI Rui, LIU Huan, YI Bo-tao, HAN Xiao-ri, LIU Yi-fei. Exogenous calcium alleviates phosphorus deficiency-induced photosynthetic inhibition in peanut (Arachis hypogaea)[J]. Journal of Plant Nutrition and Fertilizers, 2022, 28(6): 1055-1066. DOI: 10.11674/zwyf.2021514

外源钙缓解花生亚低磷光合障碍的机制

Exogenous calcium alleviates phosphorus deficiency-induced photosynthetic inhibition in peanut (Arachis hypogaea)

  • 摘要:
    目的 亚低磷胁迫是制约我国花生优质高产的一个重要因素,而外源钙可有效改善中低产田花生的生长发育和产量。为此,研究了外源钙缓解花生亚低磷光合障碍的机制。
    方法 以我国东北花生主栽品种之一‘辽宁白沙’为试验材料,以Hoagland营养液为基础,在人工气候室内进行了砂培试验。花生幼苗催芽两周后进行处理,共设4个处理:1) CK,正常磷营养液(P 1 mmol/L)+喷清水对照;2) –P,亚低磷胁迫(P 0.5 mmol/L)+喷清水;3) –P+Ca,亚低磷胁迫+叶面喷施CaCl2 15 mmol/L;4) –P+TFP,亚低磷胁迫+钙调蛋白CaM抑制剂—三氟啦嗪(trifluoperazine, TFP)。处理后第9天,测定花生功能叶片气体交换、光系统活性;第10天,取样分析幼苗生长状况和类囊体膜完整性。
    结果 亚低磷胁迫显著降低了花生的干物质积累、总叶面积和相对叶绿素含量,降低了花生叶片净光合速率P_\rmn 、蒸腾速率T_\rmr 和气孔导度G_\rms ;亚低磷胁迫显著降低了花生叶片PSⅡ实际量子产量Y(Ⅱ)、PSⅠ实际量子产量Y(Ⅰ)。与–P处理相比,–P+Ca处理显著提升了花生植株干物质积累和总叶面积,分别提高了26.7%和31.9%;改善了花生叶片的光合作用水平,显著提高了叶片净光合速率和气孔导度;外源钙提高了Y(Ⅰ)、Y(Ⅱ),明显缓解了亚低磷诱导的花生叶片Y(Ⅰ)和Y(Ⅱ)下降,提升了PQ库大小和环式电子传递,显著提高了类囊体ATP合酶活性,降低了类囊体的∆pH,缓解了类囊体腔酸化。与–P处理相比,–P+TFP处理加剧了花生类囊体膜的损伤,并进一步降低了环式电子传递速率和ATP合酶活性。
    结论 亚低磷胁迫显著限制花生的生长发育,降低了ATP合酶活性,造成了花生光抑制。外源钙能有效缓解亚低磷胁迫诱导的花生植株干物质积累、叶面积和相对叶绿素含量下降,并缓解亚低磷胁迫对光系统Ⅰ和光系统Ⅱ的抑制,而花生钙调蛋白(Ca2+-modulin)作为钙离子(Ca2+)的受体,在外源钙缓解花生亚低磷光合障碍的营养信号转导中起到重要作用。

     

    Abstract:
    Objectives The phosphorus (P) deficiency is one of the main factors limiting photosynthetic carbon fixation and high-quality yield in peanut production. Calcium can enhance peanut growth and yield in low to medium yielding farmlands. Therefore, we explored the effects of exogenous calcium on alleviating P deficiency-induced photosynthetic inhibition in peanuts.
    Methods Peanut cultivar ‘Liaoning Baisha’ was used in a pot experiment conducted in an artificial climate chamber. The P deficiency treatment was imposed by adjusting the P concentration in Hoagland nutrition solution to 0.5 mmol/L (–P) from the normal level of 1 P mmol/L. The treatments were normal P + spraying ddH2O (CK), –P + spraying ddH2O, –P + spraying CaCl2, and –P + spraying trifluoperazine (TFP, a calmodulin inhibitor). We measured the photosynthetic functions, plant growth and thylakoid membrane integrity at 9 and 10 days after treatment imposition in peanuts.
    Results Compared with CK, P deficiency reduced the dry matter weight, total leaf area, relative chlorophyll concentration and limited the growth and development of peanuts. The P deficiency reduced the net photosynthetic rate, transpiration rate, and stomatal conductance of peanut leaves. It also reduced the efficiency of PSⅠ and PSⅡ of peanuts by 18% and 5.4%, respectively. Compared with –P treatment, exogenous Ca2+ enhanced the dry matter weight and total leaf area of peanuts under P deficiency by 26.7% and 31.9%, respectively. Exogenous Ca2+ alleviated P deficiency inhibition based on photosynthetic level and enhanced the net photosynthetic rate and the stomatal conductance of peanut leaves under P deficiency. Compared with –P treatment, exogenous Ca2+ enhanced the efficiency of PSⅠ and PSⅡ, alleviating the photoinhibition in peanut leaves under P deficiency. Exogenous Ca2+ enhanced the size of the PQ pool, the rate of cyclic electron flow, and the activity of ATP synthase. However, it reduced the ∆pH of thylakoid in peanut leaves under P deficiency. TFP increased the thylakoid membrane damage, reduced cyclic electron flow rate, and ATP synthase activity in P deficiency stressed peanuts compared with –P treatment.
    Conclusions P deficiency limited the growth and development of peanuts, reduced the activity of ATP synthase of thylakoid, Y(Ⅰ), Y(Ⅱ), and caused peanut photoinhibition. Exogenous Ca2+ alleviated inhibition of the dry matter weight, total leaf area, and relative chlorophyll concentration of peanuts. Exogenous Ca2+ ralleviated the Y(Ⅰ) and Y(Ⅱ) inhibition. The peanut CaM (Ca2+-modulin) acceptor for exogenous calcium (Ca2+) played an important role in the nutritional signalling of Ca2+, alleviating photosynthetic inhibition under P deficiency.

     

/

返回文章
返回