Division of Biochemistry, ICAR-Indian Agricultural Research Institute, New Delhi, India.
Division of Biochemistry, ICAR-Indian Agricultural Research Institute, New Delhi, India.
Plant Physiol Biochem. 2020 Dec;157:239-243. doi: 10.1016/j.plaphy.2020.10.018. Epub 2020 Oct 27.
ADP glucose pyrophosphorylase (AGPase, EC 2.7.7.27) and starch synthase (SS, EC 2.4.1.21) are key regulatory enzymes involved in the starch biosynthesis. Comprehensive analysis of transcription levels of ADP-glucose pyrophosphorylase and starch synthase genes was performed in leaves, roots, and developing grains of drought susceptible (IR64) and drought-tolerant (N22) cultivars under applied water deficit stress (WDS). AGPase and SS genes are differentially regulated in leaves, roots, and grains under the drought stress. The expression pattern of SS and AGPase genes was correlated with the activity of both AGPase, SS, and starch content of developing grains under the drought. Drought stress reduced transitory starch in leaves and enhanced storage starch in developing grains. An increase in the activity of AGPase in developing grains was due to induced expression of ADP glucose pyrophosphorylase large subunit 3 (AGPL3) in N22 and both ADP glucose pyrophosphorylase small subunit 2 (AGPS2) & ADP glucose pyrophosphorylase large subunit 3 (AGPL3) in IR64 and a positive correlation was established with starch content. Similarly, an increase in the SS activity in developing grains was due to induced expression of soluble starch synthase (SSIIB, SSIVA, and SSIVB) in N22 and SSIVB in IR64.
ADP 葡萄糖焦磷酸化酶(AGPase,EC 2.7.7.27)和淀粉合酶(SS,EC 2.4.1.21)是参与淀粉生物合成的关键调节酶。在应用水分亏缺胁迫(WDS)下,对耐旱品种(N22)和耐旱品种(IR64)的叶片、根和发育中的籽粒中 ADP-葡萄糖焦磷酸化酶和淀粉合酶基因的转录水平进行了综合分析。在干旱胁迫下,AGPase 和 SS 基因在叶片、根和籽粒中受到不同的调节。SS 和 AGPase 基因的表达模式与 AGPase、SS 和发育中的籽粒淀粉含量的活性相关。干旱胁迫减少了叶片中转瞬即逝的淀粉,增加了发育中的籽粒中的储存淀粉。AGPase 在发育中的籽粒中的活性增加是由于 N22 中 ADP 葡萄糖焦磷酸化酶大亚基 3(AGPL3)的诱导表达以及 IR64 中 ADP 葡萄糖焦磷酸化酶小亚基 2(AGPS2)和 ADP 葡萄糖焦磷酸化酶大亚基 3(AGPL3)的诱导表达,并与淀粉含量呈正相关。同样,发育中的籽粒中 SS 活性的增加是由于 N22 中可溶性淀粉合酶(SSIIB、SSIVA 和 SSIVB)和 IR64 中 SSIVB 的诱导表达所致。