Hawkesbury Institute for the Environment, University of Western Sydney, Locked Bag 1797, Penrith, NSW, 2751, Australia.
ARC Centre of Excellence for Translational Photosynthesis, Australian National University, Canberra, ACT, 2601, Australia.
Photosynth Res. 2018 Nov;138(2):233-248. doi: 10.1007/s11120-018-0569-x. Epub 2018 Aug 4.
Expanding knowledge of the C photosynthetic pathway can provide key information to aid biological improvements to crop photosynthesis and yield. While the C NADP-ME pathway is well characterised, there is increasing agricultural and bioengineering interest in the comparably understudied NAD-ME and PEPCK pathways. Within this study, a systematic identification of key differences across species has allowed us to investigate the evolution of C-recruited genes in one C and eleven C grasses (Poaceae) spanning two independent origins of C photosynthesis. We present evidence for C-specific paralogs of NAD-malic enzyme 2, MPC1 and MPC2 (mitochondrial pyruvate carriers) via increased transcript abundance and associated rates of evolution, implicating them as genes recruited to perform C photosynthesis within NAD-ME and PEPCK subtypes. We then investigate the localisation of AspAT across subtypes, using novel and published evidence to place AspAT3 in both the cytosol and peroxisome. Finally, these findings are integrated with transcript abundance of previously identified C genes to provide an updated model for C grass NAD-ME and PEPCK photosynthesis. This updated model allows us to develop on the current understanding of NAD-ME and PEPCK photosynthesis in grasses, bolstering our efforts to understand the evolutionary 'path to C' and improve C photosynthesis.
扩展 C 光合作用途径的知识可以提供关键信息,有助于促进作物光合作用和产量的生物改良。虽然 C NADP-ME 途径已经得到很好的描述,但 NAD-ME 和 PEPCK 途径的研究相对较少,因此在农业和生物工程领域越来越受到关注。在本研究中,对不同物种的关键差异进行了系统的鉴定,使我们能够研究跨越 C 光合作用两次独立起源的一个 C 种和十一个 C 禾本科植物(禾本科)中 C 招募基因的进化。我们通过增加转录丰度和相关的进化速率,提供了 NAD-苹果酸酶 2、MPC1 和 MPC2(线粒体丙酮酸载体)的 C 特异性同工酶的证据,暗示它们是被招募到 NAD-ME 和 PEPCK 亚型中进行 C 光合作用的基因。然后,我们通过使用新的和已发表的证据,研究了 AspAT 在亚型中的定位,将 AspAT3 定位在细胞质和过氧化物酶体中。最后,将这些发现与先前鉴定的 C 基因的转录丰度相结合,为 C 禾本科植物 NAD-ME 和 PEPCK 光合作用提供了一个更新的模型。该更新模型使我们能够在当前对禾本科植物 NAD-ME 和 PEPCK 光合作用的理解基础上进一步发展,从而加强我们对“C 途径”进化的理解并提高 C 光合作用。