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生长素增强玉米胚芽鞘细胞壁中的葡聚糖自动水解。

Auxin-enhanced glucan autohydrolysis in maize coleoptile cell walls.

机构信息

Department of Vegetable Crops, University of California, Davis, California 95616.

出版信息

Plant Physiol. 1991 May;96(1):285-90. doi: 10.1104/pp.96.1.285.

Abstract

Cell walls isolated from auxin-pretreated maize (Zea mays L.) coleoptile segments were assayed to disclose evidence for the existence of enhanced autolysis. To improve the sensitivity of the measurements and to facilitate kinetic analysis, isolated cell walls were consolidated within a small column, and the autolysis rate was directly determined from the sugar content of the effluent. This protocol revealed that the maximum rate of autohydrolysis of walls prepared from segments occurs within the first 2 hours and a steady decline commences almost immediately. Walls from indoleacetic acid pretreated segments (0.5-4 hours) released sugar at a higher rate initially (110-125% of controls) and the enhanced rate of autolysis continued for 6 to 8 hours, but then it became equivalent to that of the controls. Pretreatment of the segments at acidic pH had no effect on the measurable rates of autolysis. The (1-->3), (1-->4)-beta-d-glucan content of the walls and the extractable glucanase activities support the hypothesis that temporal enhancement of autohydrolysis is a function of auxin on enzyme activity. The progressive decline in autolysis during prolonged incubations is consistent with the decrease in the quantity of the beta-d-glucan in the wall. The relationship between glucan content and autolysis rate is supported by the observation that while glucose pretreatment of segments had only a small effect on initial autolysis rates, the presence of the sugar during pretreatment served to extend the interval over which higher rates of autolysis could be sustained. The results demonstrate that autolysis is related to auxin-induced wall metabolism in maize coleoptiles.

摘要

从生长素预处理的玉米(Zea mays L.)胚芽鞘段分离的细胞壁进行了测定,以揭示增强自溶的证据。为了提高测量的灵敏度并便于动力学分析,将分离的细胞壁整合到一个小柱中,并直接从流出物中的糖含量来确定自溶率。该方案表明,从段制备的细胞壁的最大自水解速率在最初的 2 小时内发生,并且几乎立即开始稳定下降。吲哚乙酸预处理段(0.5-4 小时)的细胞壁最初以更高的速率释放糖(对照的 110-125%),并且增强的自溶速率持续 6 至 8 小时,但随后与对照相同。在酸性 pH 下预处理段对可测量的自溶速率没有影响。细胞壁的(1-->3),(1-->4)-β-d-葡聚糖含量和可提取的葡聚糖酶活性支持这样的假设,即自水解的时间增强是生长素对酶活性的功能。在延长孵育期间自溶的逐渐下降与壁中β-d-葡聚糖数量的减少一致。葡聚糖含量与自溶率之间的关系得到了观察结果的支持,即虽然葡萄糖预处理段对初始自溶率只有很小的影响,但在预处理期间存在该糖有助于延长可以维持更高自溶率的间隔。结果表明,自溶与玉米胚芽鞘中生长素诱导的壁代谢有关。

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