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丛枝菌根根内丛枝中碱性磷酸酶活性和多聚磷酸盐的同步原位检测。

Simultaneous in situ detection of alkaline phosphatase activity and polyphosphate in arbuscules within arbuscular mycorrhizal roots.

作者信息

Funamoto Rintaro, Saito Katsuharu, Oyaizu Hiroshi, Saito Masanori, Aono Toshihiro

机构信息

Biotechnology Research Center, The University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo 113-8657, Japan.

Faculty of Agriculture, Shinshu University, 8304 Minami-minowa, Nagano 399-4598, Japan.

出版信息

Funct Plant Biol. 2007 Sep;34(9):803-810. doi: 10.1071/FP06326.

Abstract

Inorganic phosphate (Pi) metabolism in arbuscules of arbuscular mycorrhizal (AM) fungi is not well understood, although recent research has revealed that host plants absorb Pi around arbuscules with mycorrhiza-specific transporters. Therefore, we analysed the localisation of polyphosphate (polyP) and alkaline phosphatase (ALP) activity in arbuscules, which could be indicators of Pi metabolism. We developed a dual-labelling method for polyP and ALP activity, i.e. first labelling with fluorescent probes 4',6-diamidino-2-phenyl-indole dihydrochloride (DAPI) and then labelling with enzyme-labelled fluorescence (ELF97). The dual-labelling method made it possible to observe polyP and ALP activity signals simultaneously in mycorrhizal roots. The dual-labelling method revealed that ALP activity was mainly observed in mature arbuscules where polyP was rarely observed. The expression of the AM fungal ALP gene was suppressed in the knockdown plants of an AM-inducible Pi-transporter, and there was much polyP in arbuscules that showed low ALP activity. These topological observations suggest that there may be some relationships between polyP metabolism and ALP activity in arbuscules, and that these are, in part, controlled by Pi uptake by plants via the AM-inducible Pi-transporter.

摘要

尽管最近的研究表明宿主植物通过菌根特异性转运蛋白在丛枝周围吸收无机磷酸盐(Pi),但丛枝菌根(AM)真菌丛枝中的无机磷酸盐(Pi)代谢仍未得到充分了解。因此,我们分析了丛枝中多聚磷酸盐(polyP)的定位和碱性磷酸酶(ALP)活性,它们可能是Pi代谢的指标。我们开发了一种用于多聚磷酸盐和ALP活性的双重标记方法,即先用荧光探针4',6-二脒基-2-苯基吲哚二盐酸盐(DAPI)标记,然后用酶标记荧光(ELF97)标记。这种双重标记方法使得在菌根根系中同时观察多聚磷酸盐和ALP活性信号成为可能。双重标记方法显示,ALP活性主要在成熟丛枝中观察到,而在这些成熟丛枝中很少观察到多聚磷酸盐。在AM诱导型Pi转运蛋白的敲低植物中,AM真菌ALP基因的表达受到抑制,并且在ALP活性较低的丛枝中有大量多聚磷酸盐。这些拓扑学观察结果表明,丛枝中的多聚磷酸盐代谢与ALP活性之间可能存在一些关系,并且这些关系部分受植物通过AM诱导型Pi转运蛋白吸收Pi的控制。

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