7 research outputs found
Low pH-Induced Changes of Antioxidant Enzyme and ATPase Activities in the Roots of Rice (<i>Oryza sativa</i> L.) Seedlings
<div><p>Soil acidification is the main problem in the current rice production. Here, the effects of low pH on the root growth, reactive oxygen species metabolism, plasma membrane functions, and the transcript levels of the related genes were investigated in rice seedlings (<i>Oryza sativa</i> L.) in a hydroponic system at pH 3.5, 4.5, and 5.5. There were two hybrid rice cultivars in this trial, including Yongyou 12 (YY12, a japonica hybrid) and Zhongzheyou 1 (ZZY1, an indica hybrid). Higher H<sup>+</sup> activity markedly decreased root length, the proportion of fine roots, and dry matter production, but induced a significant accumulation of hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>), and led to serious lipid peroxidation in the roots of the two varieties. The transcript levels of copper/zinc superoxide dismutase 1 (Cu/Zn SOD1), copper/zinc superoxide dismutase 2 (Cu/Zn SOD2), catalase A (CATA) and catalase B (CATB) genes in YY12 and ZZY1 roots were significantly down-regulated after low pH exposure for two weeks. Meanwhile, a significant decrease was observed in the expression of the P-type Ca<sup>2+</sup>-ATPases in roots at pH 3.5. The activities of antioxidant enzymes (SOD, CAT) and plasma membrane (PM) Ca<sup>2+</sup>-ATPase in the two varieties were dramatically inhibited by strong rhizosphere acidification. However, the expression levels of ascorbate peroxidase 1 (APX1) and PM H<sup>+</sup>-ATPase isoform 7 were up-regulated under H<sup>+</sup> stress compared with the control. Significantly higher activities of APX and PM H<sup>+</sup>-ATPase could contribute to the adaptation of rice roots to low pH.</p></div
H<sub>2</sub>O<sub>2</sub> content (A), and MDA content (B) in roots of rice (<i>Oryza sativa</i> L.) grown at three pH levels.
<p>Each value is the mean ± standard error of three replicates. Different letters for each cultivar indicate means that differ significantly (<i>P</i> < 0.05).</p
Proportion of rice (<i>Oryza sativa</i> L. A, YY12; B, ZZY1) root lengths in different diameter classes at three pH levels.
<p>Each value is the mean ± standard error of three replicates. Different letters for each cultivar indicate means that differ significantly (<i>P</i> < 0.05) within a given diameter class.</p
Plasma membrane H<sup>+</sup>-ATPase (A) and Ca<sup>2+</sup>-ATPase (B) activities derived from rice seedling in the roots of rice (<i>Oryza sativa</i> L.) grown at three pH levels.
<p>Each value is the mean ± standard error of three replicates. Different letters for each cultivar indicate means that differ significantly (<i>P</i> < 0.05).</p
Relative expression ratios (ratio of each gene to actin) of genes encoding plasma membrane H<sup>+</sup>-ATPase in the roots of rice (<i>Oryza sativa</i> L.) grown at three pH levels.
<p>Each value is the mean ± standard error of three replicates. Different letters for each cultivar indicate means that differ significantly (P < 0.05).</p
Biomass and root morphology of rice (Oryza sativa L.) seedlings grown at different pH levels.
<p>Note: Each value is the mean ± standard error of three replicates. Different letters for each cultivar indicate means that differ significantly (P < 0.05).</p><p>Biomass and root morphology of rice (Oryza sativa L.) seedlings grown at different pH levels.</p
Comparative Study of the Selective Degradations of Two Enantiomers in the Racemate and an Enriched Concentration of Indoxacarb in Soils
In
this study, selective degradations of the two enantiomers of
indoxacarb in the concentrate (2.33S/1R) and racemate (1S/1R) are
examined. The absolute configurations of indoxacarb enantiomers were
determined using X-ray diffraction. The results showed that in two
alkaline soils, the <i>S</i>-(+)-indoxacarb was preferentially
degraded in both the concentrate and racemate. In one acid soil, the
two enantiomers degraded no-selectivity. In another acid soil and
one neutral soil, the <i>R</i>-(−)-indoxacarb was
preferentially degraded in both the concentrate and racemate. Indoxacarb
enantiomers were configurationally stable in the five soils, and no
interconversion was observed during the incubation. Because no significant
difference in degradation was observed after samples were sterilized,
the observed enantioselectivity may be attributed primarily to microbial
activity in soils. The results indicate that the selective degradation
behavior was the same for both formulations that were tested