Research Article

[Retracted] Leaf Rolling and Stem Fasciation in Grass Pea (Lathyrus sativus L.) Mutant Are Mediated through Glutathione-Dependent Cellular and Metabolic Changes and Associated with a Metabolic Diversion through Cysteine during Phenotypic Reversal

Table 3

Activities of γ-glutamylcysteine synthetase (γ-ECS, nmol min−1 g−1 FW), serine acetyl transferase (SAT, U mg−1 protein), O-acetylserine thiol lyase (OAS-TL, nmol cysteine min−1 mg−1 protein), superoxide dismutase (SOD, U min−1 mg−1 protein), ascorbate peroxidase (APX, µmol ascorbate oxidized min−1 mg−1 protein), glutathione reductase (GR, nmol NADPH oxidized min−1 mg−1 protein), glutathione-S transferases (GSTs, U mg−1 protein), and glutathione peroxidase (GPX, nmol NADPH min−1 mg−1 (protein)), L-cysteine desulfhydrase (LCD, nmol H2S min−1 mg−1 protein), D-cysteine desulfhydrase (DCD, nmol H2S min−1 mg−1 protein), hydrogen sulfide level (H2S, µmol g−1 FW) and glycolate oxidase (GO, µmol glyoxylate min−1 mg−1 protein) H2O2 (µmol g−1 FW), malondialdehyde (MDA, nmol g−1 FW) in rlfL-1 mutant and its mother variety Biol-212 under untreated and BSO-treated conditions.

TraitsMCMuCMuTTM

γ-ECS NDND
SAT
OAS-TL
SOD-leaf
SOD-stems
APX-leaf
APX-stems
GR-leaf
GR-stems
GSTs-leaf
GSTs-stem
GPX-leaf
GPX-stems
LCD-leaf
LCD-stems
DCD-leaf
DCD-stems
H2S level-leaf
H2S level-stems
GO activity-leaf
H2O2-leaf
H2O2-stem
MDA-leaf
MDA-stems
EL%-leaf
EL%-stems 25.58 ± 0.50

Data are means ± SE of at least four replicates. Means followed by same alphabets are not significantly ( > 0.05) different at ANOVA followed by Duncan’s multiple range test. MC-untreated (no BSO) mother control, MuC-untreated (no BSO), MuT-BSO-treated mutant, and TM-BSO treated mother plant.