...
首页> 外文期刊>Cellulose >Antibodies against a Gossypium hirsutum recombinant cellulose synthase (Ces A) specifically label cellulose synthase in Micrasterias denticulata
【24h】

Antibodies against a Gossypium hirsutum recombinant cellulose synthase (Ces A) specifically label cellulose synthase in Micrasterias denticulata

机译:一种针对陆地棉重组纤维素合酶(Ces A)的抗体,可特异性标记牙本质草中的纤维素合酶

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Using immunocytochemistry combined with light and electron microscopy, antibodies against cotton ( Gossypium hirsutum) Ces A3 were used to identify and localize Ces A proteins in Micrasterias denticulata. Silver-enhanced, immuno-gold labeling of Ces A was localized on the plasma membrane with light and immuno-electron microscopy. Immuno-gold labeling of beta-1,4-glucan synthase always was observed in contact with the tips of negatively stained cellulose microfibrils. Although the beta-1,4-glucan synthesizing system in the cell wall of Micrasterias denticulata has been investigated by several methods in the past few decades, these results provide the first significant evidence that the hexagonal arrays of 'rosettes' observed in the freeze-etch replica techniques within the plasma membrane of Micrasterias denticulata are beta-1, 4-glucan synthases. In addition, the antibodies to cotton Ces A3 show no reactivity with beta-1,4-glucan synthases from Boergesenia forbesii ( a Siphonocladaceaen alga with linear terminal complexes = TCs). These results suggest that the specific morphology of TCs ( e. g., rosette or linear arrangement) is closely related to the cellulose synthase antibody binding sites ( catalytic domains). These data are consistent with a recent phylogenic analysis which shows that Mesotaenium caldariorum possesses Ces A-type genes that are closely related to Ces A's in vascular plants. This report suggests a significant divergence between the cellulose synthase catalytic subunits of the Chlorophyta ( linear TCs) and the Streptophyta ( rosette TCs).
机译:使用免疫细胞化学结合光学和电子显微镜,针对棉花(棉)Ces A3的抗体被用于鉴定和定位小叶草中的Ces A蛋白。用光镜和免疫电子显微镜将Ces A的银增强免疫金标记定位在质膜上。总是在与阴性染色的纤维素微纤维尖端接触时观察到β-1,4-葡聚糖合酶的免疫金标记。尽管过去几十年来已通过多种方法研究了小Mi草细胞壁中的β-1,4-葡聚糖合成系统,但这些结果提供了第一个重要证据,即在冷冻状态下观察到的“玫瑰花”的六边形阵列米氏微藻质膜内的蚀刻复制技术是β-1、4-葡聚糖合酶。此外,抗棉Ces A3的抗体与来自Boergesenia forbesii的β-1,4-葡聚糖合酶(具有线性末端复合物的虹吸藻藻类= TCs)没有反应。这些结果表明TC的特定形态(例如,玫瑰花结或线性排列)与纤维素合酶抗体结合位点(催化结构域)密切相关。这些数据与最近的系统发育分析一致,该分析表明,中空介球藻具有与维管植物中的Ces A密切相关的Ces A型基因。该报告表明,在绿藻(线性TCs)和链霉菌(玫瑰花TCs)的纤维素合酶催化亚基之间存在显着差异。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号