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Browsing by Author "Vemula, Chandra Kaladhar"

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    Moderate modulation by S-nitrosoglutathione of photorespiratory enzymes in pea (Pisum sativum) leaves, compared to the strong effects of high light
    (Springer Nature Publishing AG, 2024) Saini, Deepak; Bapatla, Ramesh B.; Vemula, Chandra Kaladhar; Gahir, Shashibhushan; Bharath, Pulimamidi; Gupta, Kapuganti Jagadis; Raghavendra, Agepati S.
    When plants are exposed to water stress, photosynthesis is downregulated due to enhanced reactive oxygen species (ROS) and nitric oxide (NO). In contrast, photorespiratory metabolism protected photosynthesis and sustained yield. Modulation of photorespiration by ROS was established, but the effect of NO on photorespiratory metabolism was unclear. We, therefore, examined the impact of externally added NO by using S-nitrosoglutathione (GSNO), a natural NO donor, in leaf discs of pea (Pisum sativum) under dark or light: moderate or high light (HL). Maximum NO accumulation with GSNO was under high light. The presence of 2-4-carboxyphenyl-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide (cPTIO), a NO scavenger, prevented the increase in NO, confirming the release of NO in leaves. The increase in S-nitrosothiols and tyrosine-nitrated proteins on exposure to GSNO confirmed the nitrosative stress in leaves. However, the changes by GSNO in the activities and transcripts of five photorespiratory enzymes: glycolate oxidase, hydroxypyruvate reductase, catalase, glycerate kinase, and phosphoglycolate phosphatase activities were marginal. The changes in photorespiratory enzymes caused by GSNO were much less than those with HL. Since GSNO caused only mild oxidative stress, we felt that the key modulator of photorespiration might be ROS, but not NO.
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    Nitric oxide-mediated modulation of photorespiratory enzymes and photochemical components in leaves of pea plants (Pisum sativum)
    (John Wiley & Sons, 2026) Saini, Deepak; Bharath, Pulimamidi; Gahir, Shashibhushan; Pandey, Jayendra; Vemula, Chandra Kaladhar; Gupta, Kapuganti Jagadis; Subramanyam, Rajagopal; Raghavendra, Agepati S
    The photorespiratory metabolism safeguards photosynthesis against abiotic and biotic stress. Nitric oxide (NO) and reactive oxygen species (ROS) levels rise in plants during abiotic stress. Low concentrations of NO or ROS are beneficial as signalling molecules, but they can be toxic to plant cells at high concentrations. ROS are known to modulate photorespiration; however, it is unclear whether NO affects photorespiratory enzymes and photochemical components simultaneously. We therefore used sodium nitroprusside (SNP) under dark, moderate light (ML), or high light (HL) conditions to simultaneously investigate its impact on photorespiratory enzymes and photochemical components. The NO levels were increased upon SNP exposure in Pisum sativum leaves, particularly under HL conditions. The NO release in leaves was confirmed when the NO scavenger cPTIO (2-(4-Carboxyphenyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide potassium salt) was present, since it decreased the majority of elevated NO. The nitrosative/oxidative stress in Pisum sativum leaves was confirmed by the increase in nitrosothiols and tyrosine-nitrated proteins, as well as reduced aconitase activity after SNP exposure at HL. The protein levels, mRNA levels, and the enzyme activities of the following four photorespiratory enzymes: glycolate oxidase (GO), hydroxypyruvate reductase (HPR), glycerate kinase (GK), and phosphoglycolate phosphatase (PGLP) were markedly increased under elevated NO conditions. Catalase (CAT), ascorbate peroxidase (APX), and superoxide dismutase (SOD) also showed increased activity, elevated protein and transcript levels upon exposure to SNP. Parallel studies on chlorophyll a fluorescence confirmed that NO restricted electron transport at both PSII and PSI, inhibited photosynthesis and respiration, and damaged photosynthetic pigments. We concluded from this study that NO at high concentrations upregulated photorespiratory enzymes while inhibiting photochemical components such as photosystem II and I (PSII/PSI) simultaneously.

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