The NAD Kinase Slr0400 Functions as a Growth Repressor in Synechocystis sp. PCC 6803.

Ishikawa, Yuuma; Cassan, Cedric; Kadeer, Aikeranmu; Yuasa, Koki; Sato, Nozomu; Sonoike, Kintake; Kaneko, Yasuko; Miyagi, Atsuko; Takahashi, Hiroko; Ishikawa, Toshiki; Yamaguchi, Masatoshi; Nishiyama, Yoshitaka; Hihara, Yukako; Gibon, Yves; Kawai-Yamada, Maki

NADP , the phosphorylated form of nicotinamide adenine dinucleotide (NAD), plays an essential role in many cellular processes. NAD kinase (NADK), which is conserved in all living organisms, catalyzes the phosphorylation of NAD to NADP . However, the physiological role of phosphorylation of NAD to NADP in the cyanobacterium Synechocystis remains unclear. In this study, we report that slr0400 , an NADK-encoding gene in Synechocystis , functions as a growth repressor under light-activated heterotrophic growth conditions and light and dark cycle conditions in the presence of glucose. We show, via characterization of NAD(P)(H) content and enzyme activity, that NAD accumulation in slr0400 -deficient mutant results in the unsuppressed activity of glycolysis and tricarboxylic acid (TCA) cycle enzymes. In determining whether Slr0400 functions as a typical NADK, we found that constitutive expression of slr0400 in an Arabidopsis nadk2 -mutant background complements the pale-green phenotype. Moreover, to determine the physiological background behind the growth advantage of mutants lacking slr04000 , we investigated the photobleaching phenotype of slr0400 -deficient mutant under high-light conditions. Photosynthetic analysis found in the slr0400 -deficient mutant resulted from malfunctions in the Photosystem II (PSII) photosynthetic machinery. Overall, our results suggest that NADP(H)/NAD(H) maintenance by slr0400 plays a significant role in modulating glycolysis and the TCA cycle to repress the growth rate and maintain the photosynthetic capacity.

NAD (Coenzyme); SYNECHOCYSTIS; PHOTOSYSTEMS; TRICARBOXYLIC acids; PHENOTYPES; PHOSPHORYLATION

Plant & Cell Physiology, 2021, Vol 62, Issue 4, p668

0032-0781

Academic Journal

10.1093/pcp/pcab023