» Articles » PMID: 38902617

A Comprehensive Assessment of Photosynthetic Acclimation to Shade in C4 Grass (Cynodon Dactylon (L.) Pers.)

Overview
Journal BMC Plant Biol
Publisher Biomed Central
Specialty Biology
Date 2024 Jun 20
PMID 38902617
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Light deficit in shaded environment critically impacts the growth and development of turf plants. Despite this fact, past research has predominantly concentrated on shade avoidance rather than shade tolerance. To address this, our study examined the photosynthetic adjustments of Bermudagrass when exposed to varying intensities of shade to gain an integrative understanding of the shade response of C4 turfgrass.

Results: We observed alterations in photosynthetic pigment-proteins, electron transport and its associated carbon and nitrogen assimilation, along with ROS-scavenging enzyme activity in shaded conditions. Mild shade enriched Chl b and LHC transcripts, while severe shade promoted Chl a, carotenoids and photosynthetic electron transfer beyond Q (ET/RC, φE, Ψ). The study also highlighted differential effects of shade on leaf and root components. For example, Soluble sugar content varied between leaves and roots as shade diminished SPS, SUT1 but upregulated BAM. Furthermore, we observed that shading decreased the transcriptional level of genes involving in nitrogen assimilation (e.g. NR) and SOD, POD, CAT enzyme activities in leaves, even though it increased in roots.

Conclusions: As shade intensity increased, considerable changes were noted in light energy conversion and photosynthetic metabolism processes along the electron transport chain axis. Our study thus provides valuable theoretical groundwork for understanding how C4 grass acclimates to shade tolerance.

References
1.
Sonawane B, Sharwood R, Whitney S, Ghannoum O . Shade compromises the photosynthetic efficiency of NADP-ME less than that of PEP-CK and NAD-ME C4 grasses. J Exp Bot. 2018; 69(12):3053-3068. PMC: 5972597. DOI: 10.1093/jxb/ery129. View

2.
Testerink C, Dekker H, Lim Z, Johns M, Holmes A, Koster C . Isolation and identification of phosphatidic acid targets from plants. Plant J. 2004; 39(4):527-36. DOI: 10.1111/j.1365-313X.2004.02152.x. View

3.
Yu W, Peng F, Wang W, Liang J, Xiao Y, Yuan X . SnRK1 phosphorylation of SDH positively regulates sorbitol metabolism and promotes sugar accumulation in peach fruit. Tree Physiol. 2021; 41(6):1077-1086. PMC: 8190949. DOI: 10.1093/treephys/tpaa163. View

4.
Cho Y, Yoo S, Sheen J . Glucose signaling through nuclear hexokinase1 complex in Arabidopsis. Plant Signal Behav. 2009; 2(2):123-4. PMC: 2633915. DOI: 10.4161/psb.2.2.3894. View

5.
Bou-Torrent J, Toledo-Ortiz G, Ortiz-Alcaide M, Cifuentes-Esquivel N, Halliday K, Martinez-Garcia J . Regulation of Carotenoid Biosynthesis by Shade Relies on Specific Subsets of Antagonistic Transcription Factors and Cofactors. Plant Physiol. 2015; 169(3):1584-94. PMC: 4634050. DOI: 10.1104/pp.15.00552. View