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Induction of (1→3,1→4)-β-D-glucan hydrolases in leaves of dark-incubated barley seedlings

机译:暗温大麦幼苗叶片中(1→3,1→4)-β-D-葡聚糖水解酶的诱导

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摘要

When seedlings of barley (Hordeum vulgare L.) were transferred from a natural light/dark cycle into darkness, (1→3,1→4)-β-D-glucan endohydrolase (EC 3.2.1.73) activity in leaf extracts increased 3- to 4-fold after 2 days. Activity decreased to normal levels within a day if the light/dark cycle was restored. Although there are two (1→3,1→4)-β-D-glucan endohydrolase isoenzymes in barley, the increased enzyme activity in dark-grown seedlings was attributable entirely to increases in isoenzyme EI. Northern hybridization analyses confirmed that mRNA transcripts encoding (1→3,1→4)-β-D-glucan endohydrolase isoenzyme EI accumulated in the leaves of dark-incubated seedlings; no isoenzyme EII mRNA was detected. Activity of β-D-glucan glucohydrolases also increased 10-fold after 2 days of dark treatment. The latter, broad-specificity enzymes release glucose from (1→3,1→4)-β-D-glucans and from β-D-oligoglucosides released by (1→3,1→4)-β-D-glucan endohydrolases. Consistent with the activity patterns of these enzymes, the (1→3,1→4)-β-D-glucan content of leaf cell walls decreased by about 30% when barley seedlings were transferred into darkness. Soluble sugars in the leaves decreased by about 60% during the same period. Because no measurable leaf elongation was detected during the various light/dark treatments, the enzymes were unlikely to be participating in wall loosening and cell elongation. Instead, the results suggest that cell wall (1→3,1→4)-β-D-glucans can be re-mobilized in the non-elongating, dark-incubated leaves and the glucose so generated could serve as an energy source under conditions of sugar depletion.
机译:当大麦(Hordeum vulgare L.)幼苗从自然光照/黑暗循环转移到黑暗时,叶提取物中的(1→3,1→4)-β-D-葡聚糖内切酶(EC 3.2.1.73)活性增加3 -2天后变为4倍。如果恢复了明/暗循环,一天之内的活动就会降至正常水平。虽然大麦中有两种(1→3,1→4)-β-D-葡聚糖内切酶同工酶,但黑苗中酶活性的增加完全归功于同工酶EI的增加。 Northern杂交分析证实,编码(1→3,1→4)-β-D-葡聚糖内切酶同工酶EI的mRNA转录物在黑暗培养的幼苗叶片中积累。没有检测到同工酶EII mRNA。在黑暗处理2天后,β-D-葡聚糖葡糖水解酶的活性也增加了10倍。后者,宽特异性酶从(1→3,1→4)-β-D-葡聚糖和(1→3,1→4)-β-D-葡聚糖内切酶释放的β-D-寡糖苷释放葡萄糖。与这些酶的活性模式一致,当大麦幼苗转移到黑暗中时,叶细胞壁的(1→3,1→4)-β-D-葡聚糖含量降低了约30%。在同一时期,叶子中的可溶性糖减少了约60%。由于在各种明/暗处理过程中均未检测到可测的叶片伸长,因此这些酶不太可能参与壁松和细胞伸长。取而代之的是,结果表明细胞壁(1→3,1→4)-β-D-葡聚糖可以在非延长的,黑暗培养的叶片中重新动员,并且所产生的葡萄糖可以作为能量来源。糖耗的条件。

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