Burchard R P, Bloodgood R A
Department of Biological Sciences, University of Maryland Baltimore County 21228.
J Bacteriol. 1990 Jun;172(6):3379-87. doi: 10.1128/jb.172.6.3379-3387.1990.
Surface proteins of the gliding bacterium Cytophaga sp. strain U67 that make contact with glass substrata were radioiodinated, using a substratum-immobilized catalyst (Iodo-Gen). At least 15 polypeptides were iodinated, fewer than the number labeled by surface biotinylation of whole cells; these polypeptides define the set of possible candidates for the surface protein(s) that mediates gliding-associated substratum adhesion. The labeling of three adhesion-defective mutants exhibited two characteristic patterns of surface iodination which involved addition, loss, or alteration of several polypeptides of high molecular weight. An adhesion-competent revertant of mutant Adh3 and one of Adh2 exhibited the wild-type labeling pattern. Two other Adh2 revertants resembled their adhesion-defective parent. The labeling pattern of surface polypeptides of a nongliding but adhesive cell strain was similar to that of the wild type.
利用固定在基质上的催化剂(碘甘醚)对滑行细菌噬纤维菌属菌株U67中与玻璃基质接触的表面蛋白进行放射性碘化标记。至少有15种多肽被碘化,其数量少于全细胞表面生物素化标记的数量;这些多肽确定了介导与滑行相关的基质黏附的表面蛋白的可能候选物。三个黏附缺陷突变体的标记显示出两种特征性的表面碘化模式,涉及几种高分子量多肽的增加、缺失或改变。突变体Adh3和Adh2的一个具有黏附能力的回复突变体表现出野生型标记模式。另外两个Adh2回复突变体与其黏附缺陷亲本相似。一个非滑行但具有黏附性的细胞菌株的表面多肽标记模式与野生型相似。