Choi A H, O'Day D H
J Bacteriol. 1984 Jan;157(1):291-6. doi: 10.1128/jb.157.1.291-296.1984.
Calcofluor White ST was used to monitor the morphological events in the biogenesis of cellulose in the microcyst wall of the wild-type strain (WS-320) and two developmental mutants (mic-1 and mic-2) of Polysphondylium pallidum. During encystment, the cell surface acquires a Calcofluor-specific material which appears to be cellulose because of its sensitivity to purified cellulase. Cellulose-containing vesicles appear distributed throughout the cytoplasm of encysting cells of the three strains. Later, the cellulose-rich vesicles appear near the cell surface. Subsequently, the cell surface stains with Calcofluor, and the vesicles are no longer detectable. Intracellular vesicles resembling the cellulose-rich vesicles in size, in the timing of appearance, and in cellular location are also seen in thin sections. These vesicles are surrounded by a single unit membrane, and their amorphous matrix, which contains a dense irregular core, further implicates them as the basis for the bilayered microcyst wall.
用荧光增白剂ST监测了野生型菌株(WS - 320)以及苍白聚孢黏菌的两个发育突变体(mic - 1和mic - 2)微囊壁中纤维素生物合成的形态学事件。在包囊形成过程中,细胞表面获得一种荧光增白剂特异性物质,由于其对纯化纤维素酶敏感,该物质似乎是纤维素。含纤维素的囊泡似乎分布在这三个菌株包囊化细胞的整个细胞质中。之后,富含纤维素的囊泡出现在细胞表面附近。随后,细胞表面被荧光增白剂染色,囊泡不再可检测到。在薄片中也可见到在大小、出现时间和细胞位置上与富含纤维素的囊泡相似的细胞内囊泡。这些囊泡被单层单位膜包围,其无定形基质包含一个致密的不规则核心,进一步表明它们是双层微囊壁的基础。