Light promotes the synthesis of lignin through the production of H2O2 mediated by diamine oxidases in soybean hypocotyls.

In order to analyze the relationship between polyamine oxidative degradation induced by light and the Lignin synthesis in cell walls, the activities of diamine oxidases and peroxidase, the contents of H2O2 and lignin, and the growth of hypocotyls in soybean [Glycine max (Linn.) Merr.] grown under tight or in darkness were investigated. In comparison with the dark treatment, light irradiation significantly inhibited the growth of soybean hypocotyls and promoted the activities of diamine oxidases and peroxidase as well as the accumulation of H2O2 and lignin. Treatments with the different concentrations of diamine oxidase inhibitors (2-hydroxyethylhydrazine and aminoguanidine) under the light condition inhibited diamine oxidase activity, and decreased the contents of H2O2 and lignin. The results provide evidence for the hypothesis that light irradiation could promote the accumulation of H2O2 and lignin in cell walls by activating polyamine oxidative degradation mediated by diamine oxidases.

[Mechanism of heavy metal ions on RNase activity from bovine pancreas].

This paper studied mechanism of Ce3+, Cd2+, Pb2+ on RNase activity from bovine pancreas. The results showed that the activity of RNase was enhanced under the treatment by Ce3+, Cd2+, Pb2+ at lower concentration (10-60 or 10-30 mumol.L-1), but was inhibited by Ce3+, Cd2+, Pb2+ at higher concentration (40 or 70 mumol.L-1 above), and the inhibition was in the order as Pb2+ > Cd2+ > Ce3+. The equilibrium dialysis demonstrates that RNase may have one Ca(2+)-binding site. The fluorescence titration showed that one molecule of RNase has one binding site for Ce3+, the association constant k for its low-affinity Ce(3+)-binding site is 1.22 x 10(8) L.mol-1. However, it can bind three Cd2+ or Pb2+ and the association causing constant k for its low-affinity Cd2+ or Pb(2+)-binding site is 1.8 x 10(8) L.mol-1, 2.01 x 10(8) L.mol-1, respectively, and caused the conformational changes of RNase.

Polyamine-induced nitric oxide generation and its potential requirement for peroxide in suspension cells of soybean cotyledon node callus.

Polyamines (PAs) induce nitric oxide (NO) generation in plant tissues; however, their mechanism is still unclear. In the present study, suspension cells of soybean cotyledon-node callus were employed. Using a NO-specific fluorescent dye, DAF-FM-DA (3-amino, 4-aminomethyl-2', 7'-difluorescein, diacetate), and laser confocal scanning microscopy, changes in NO generation induced by exogenous PAs were examined. The results of this study showed that NO fluorescence was significantly induced above endogenous levels when callus cells were treated with 0.05 mM PAs. However, putrescine (Put) was the most active PA. The observed NO release by PAs was rapid and without an apparent lag phase. The response was quenched when the suspension cells were treated with the NO-specific scavenger cPTIO (2-(4-carboxyphenyl)-4,4,5,5-tetramethylimidazoline-1-1-oxy-3-oxide). When 0.01 mM l-aminoguanidine (L-AG) was applied prior to the PA treatments, the NO fluorescence was diminished, and the inhibition of NO fluorescence was correlated with a decrease in diamine oxidase (DAO) activity. When callus cells were incubated with 0.1 mM catalase (CAT) and 1.0 mM N'N-dimethylthiourea (DMTU) prior to PA application, NO release was significantly reduced. In sum, our data provided evidence for PA-induced NO generation in suspension cells of soybean cotyledon node callus and demonstrated that peroxide, potentially derived from PA oxidative degradation, was involved in NO release induced by PAs.