首页> 外文期刊>Tree Physiology >Immunohistochemical localization of enzymes that catalyze the long sequential pathways of lignin biosynthesis during differentiation of secondary xylem tissues of hybrid aspen (Populus sieboldii x Populus grandidentata).
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Immunohistochemical localization of enzymes that catalyze the long sequential pathways of lignin biosynthesis during differentiation of secondary xylem tissues of hybrid aspen (Populus sieboldii x Populus grandidentata).

机译:酶的免疫组织化学定位,可在杂种白杨次生木质部组织(Populus sieboldii x Populus grandidentata)分化过程中催化木质素生物合成的长序列途径。

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We have investigated the spatial localization of enzymes that catalyze the sequential pathways of lignin biosynthesis in developing secondary xylem tissues of hybrid aspen (Populus sieboldii Miq. x Populus grandidentata Michx.) using immunohistochemical techniques. The enzymes phenylalanine ammonia-lyase, caffeic acid 3-O-methyltransferase and 4-coumarate:CoA ligase in the common phenylpropanoid pathway, cinnamyl-alcohol dehydrogenase (CAD) and peroxidase in the specific lignin pathway, 3-deoxy-D-arabino-heptulosonate 7-phosphate synthase (DAHPS) in the shikimate pathway and glutamine synthetase (GS) in the nitrogen reassimilation system were abundantly localized in the 6th to 9th wood fibers away from cambium; these wood fibers are likely undergoing the most intense lignification. Only weak immunolabeling of enzymes involved in the general phenylpropanoid and specific lignin pathways was detected in the cells near the cambium; lignification of these cells has likely been initiated after primary cell wall formation. In contrast, distinct localization of DAHPS and GS was observed around the cambium, which may be involved not only in lignin biosynthesis, but also in amino acid and protein synthesis, which are essential for cell survival. Our observations suggest that co-localization of enzymes related to the sequential shikimate, general phenylpropanoid and specific lignin branch pathways and to the nitrogen recycling system is associated with cell wall lignification of wood fibers during secondary xylem development.
机译:我们已经研究了使用免疫组织化学技术催化木质素生物合成的顺序路径的酶的空间定位,所述木质素在杂交白杨(Populus sieboldii Miq。x Populus grandidentata Michx。)的次生木质部组织的发育中。苯丙氨酸途径中的苯丙氨酸氨裂合酶,咖啡酸3-O-甲基转移酶和4-香豆酸酯:CoA连接酶,特定木质素途径中的肉桂酸-醇脱氢酶(CAD)和过氧化物酶,3-脱氧-D-阿拉伯糖- iki草酸途径中的庚二酸7-磷酸合酶(DAHPS)和氮重吸收系统中的谷氨酰胺合成酶(GS)大量位于远离形成层的第6至第9木纤维中。这些木纤维可能会经历最强烈的木质化。在形成层附近的细胞中仅检测到了与一般苯丙氨酸和特定的木质素途径有关的酶的弱免疫标记。这些细胞的木质化很可能在原代细胞壁形成后开始。相反,在形成层周围观察到了DAHPS和GS的独特定位,这不仅可能参与木质素的生物合成,而且可能参与氨基酸和蛋白质的合成,这对于细胞存活至关重要。我们的观察结果表明,与继发的iki草酸酯,一般的苯丙烷和特定的木质素分支途径以及氮循环系统相关的酶的共定位与木质部纤维在次生木质部发育过程中的细胞壁木质化有关。

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