New Factors for Protoplast-Callose-Fiber Formation in Salt-Tolerant Mangrove Plants, Avicennia alba and Bruguiera sexangula and Analysis of Fiber Substructures

Asami Kurita-Tashiro, N. Hayashi, Tomoya Oyanagi, H. Sasamoto
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引用次数: 2

Abstract

Elongated and spiral β-1,3-glucan (callose) fibers were obtained by new factors from protoplasts cultured in liquid medium from suspension cultured cells of two salt-tolerant mangrove species; Avicennia alba and Bruguiera sexangula. Differences in salt factor for protoplast-fiber formation were compared with those of the callose fibers developed from protoplasts of non-mangrove tree plants, Larix leptolepis and Betula platyphylla, which high concentrations of divalent cations, Mg2+ (50 mM) or Ca2+ (100 mM), were stimulatory. In the halophilic A. alba protoplasts, whose cell division was stimulated by up to 400 mM NaCl, addition of Mg2+, Ca2+, K+ ions inhibited protoplast-fiber formation. In B. sexangula, protoplast-fibers were rapidly and efficiently formed only by another new factor, electric cell fusion treatment of protoplasts. Spiral fibers developed from mangrove protoplasts were detected under an inverted microscope, and their specific blue-green color for callose after staining with Aniline Blue dye was detected under a fluorescence microscope. Enzymatic certification of callose was further performed with laminarinase, specific for callose, in comparison with cellulase CBH1, specific for cellulose. Differences in sub-structures, fibrils and sub-fibrils of two mangrove protoplast-fibers were analyzed using laser confocal scanning microscopy, atomic force microscopy and image J analysis. Tube-like fine structure was observed using transmission electron microscopy in single protoplast-fiber of B. sexangula selected with a micromanipulator.
红树耐盐原生质体-胼胝质纤维形成的新因素及纤维亚结构分析
从两种耐盐红树悬浮液培养的原生质体中,利用新因子获得了细长和螺旋形的β-1,3-葡聚糖(胼胶)纤维;白翅海棠和黄翅海棠。在高浓度的二价阳离子Mg2+ (50 mM)和Ca2+ (100 mM)的刺激下,比较了原生质体纤维形成的盐因子与非红树植物落叶松和白桦原生质体胼胝质纤维形成的盐因子差异。在高达400 mM NaCl刺激嗜盐藻原生质体细胞分裂的过程中,Mg2+、Ca2+、K+离子的加入抑制了原生质体纤维的形成。在六角藻中,原生质体纤维的快速有效形成需要另一个新的因素,即原生质体的细胞融合处理。倒置显微镜下检测了红树原生质体发育的螺旋纤维,荧光显微镜下检测了苯胺蓝染色后的胼胝质的蓝绿色。与纤维素酶CBH1相比,对胼胝质进行了进一步的酶鉴定,该酶是胼胝质的特异性酶。采用激光共聚焦扫描显微镜、原子力显微镜和图像J分析分析了两种红树原生质体纤维的亚结构、原纤维和亚原纤维的差异。用微操机对六角藻单根原生质体纤维进行筛选,透射电镜观察到其具有管状精细结构。
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