Lancaster Environment Centre, Lancaster University, Lancaster LA1 4YQ, U.K.
Biochem J. 2024 Aug 7;481(15):1043-1056. doi: 10.1042/BCJ20240209.
Rubisco activity is highly regulated and frequently limits carbon assimilation in crop plants. In the chloroplast, various metabolites can inhibit or modulate Rubisco activity by binding to its catalytic or allosteric sites, but this regulation is complex and still poorly understood. Using rice Rubisco, we characterised the impact of various chloroplast metabolites which could interact with Rubisco and modulate its activity, including photorespiratory intermediates, carbohydrates, amino acids; as well as specific sugar-phosphates known to inhibit Rubisco activity - CABP (2-carboxy-d-arabinitol 1,5-bisphosphate) and CA1P (2-carboxy-d-arabinitol 1-phosphate) through in vitro enzymatic assays and molecular docking analysis. Most metabolites did not directly affect Rubisco in vitro activity under both saturating and limiting concentrations of Rubisco substrates, CO2 and RuBP (ribulose-1,5-bisphosphate). As expected, Rubisco activity was strongly inhibited in the presence of CABP and CA1P. High physiologically relevant concentrations of the carboxylation product 3-PGA (3-phosphoglyceric acid) decreased Rubisco activity by up to 30%. High concentrations of the photosynthetically derived hexose phosphates fructose 6-phosphate (F6P) and glucose 6-phosphate (G6P) slightly reduced Rubisco activity under limiting CO2 and RuBP concentrations. Biochemical measurements of the apparent Vmax and Km for CO2 and RuBP (at atmospheric O2 concentration) and docking interactions analysis suggest that CABP/CA1P and 3-PGA inhibit Rubisco activity by binding tightly and loosely, respectively, to its catalytic sites (i.e. competing with the substrate RuBP). These findings will aid the design and biochemical modelling of new strategies to improve the regulation of Rubisco activity and enhance the efficiency and sustainability of carbon assimilation in rice.
Rubisco 活性受到高度调控,通常会限制作物中碳的同化。在叶绿体中,各种代谢物可以通过与 Rubisco 的催化或变构位点结合来抑制或调节 Rubisco 活性,但这种调控非常复杂,目前仍知之甚少。我们使用水稻 Rubisco 来表征各种可能与 Rubisco 相互作用并调节其活性的叶绿体代谢物的影响,包括光呼吸中间产物、碳水化合物、氨基酸;以及已知能抑制 Rubisco 活性的特定糖磷酸——CABP(2-羧基-D-阿拉伯糖醇 1,5-双磷酸)和 CA1P(2-羧基-D-阿拉伯糖醇 1-磷酸),这是通过体外酶促测定和分子对接分析得出的。在 Rubisco 底物 CO2 和 RuBP(核酮糖 1,5-二磷酸)的饱和和限制浓度下,大多数代谢物并没有直接影响体外的 Rubisco 活性。正如预期的那样,CABP 和 CA1P 的存在强烈抑制了 Rubisco 活性。生理相关浓度的羧化产物 3-PGA(3-磷酸甘油酸)使 Rubisco 活性降低了 30%。在限制 CO2 和 RuBP 浓度下,高浓度的光合作用衍生六碳磷酸果糖 6-磷酸(F6P)和葡萄糖 6-磷酸(G6P)会略微降低 Rubisco 活性。对 CO2 和 RuBP 的表观 Vmax 和 Km(在大气 O2 浓度下)的生化测量和对接相互作用分析表明,CABP/CA1P 和 3-PGA 通过紧密和松散地结合 Rubisco 的催化位点(即与底物 RuBP 竞争)来抑制 Rubisco 活性。这些发现将有助于设计和生化建模新策略,以改善 Rubisco 活性的调控,提高水稻中碳同化的效率和可持续性。