Cheng K J, Costerton J W
Appl Environ Microbiol. 1977 Nov;34(5):586-90. doi: 10.1128/aem.34.5.586-590.1977.
Of the 54 strains of rumen bacteria examined for alkaline phosphatase (APase) production, 9 of 33 gram-negative strains and none of 21 gram-positive strains produced the enzyme. The APase of the cells of the three strains of Bacteroides ruminicola that produced significant amounts of the enzyme was located in the periplasmic area of the cell envelope, whereas the enzyme was located in the strains of Selenomonas ruminantium and Succinivibrio dextrinosolvens was associated with the outer membrane. The localization of APase production in the cells of natural populations of rumen bacteria from hay-fed sheep was accomplished by reaction product deposition, and both the proportion of APase-producing bacteria and the location of the enzyme in the cell envelope of the producing cells could be determined. We suggest that this procedure is useful in detecting shifts in the bacterial population and the release of cell-bound APase that accompany feedlot bloat and other sequelae of dietary manipulation in ruminants.
在所检测的54株瘤胃细菌中,用于检测碱性磷酸酶(APase)产生情况,33株革兰氏阴性菌中有9株产生该酶,而21株革兰氏阳性菌均未产生该酶。三株产大量该酶的反刍拟杆菌细胞的碱性磷酸酶位于细胞膜的周质区域,而反刍月形单胞菌和右旋糖琥珀酸弧菌菌株中的该酶与外膜相关。通过反应产物沉积确定了干草喂养绵羊瘤胃细菌自然群体细胞中碱性磷酸酶产生的定位,并且可以确定产生碱性磷酸酶的细菌比例以及该酶在产生细胞的细胞膜中的位置。我们认为该方法有助于检测细菌群体的变化以及与饲养场瘤胃臌气和反刍动物饮食调控的其他后遗症相关的细胞结合碱性磷酸酶的释放。