Evinger M, Agabian N
J Bacteriol. 1977 Oct;132(1):294-301. doi: 10.1128/jb.132.1.294-301.1977.
Envelope-associated nucleoids have been isolated from Caulobacter crescentus by using a modification of the procedure of T. Kornberg et al. (Proc. Natl. Acad. Sci. U.S.A. 71:3189-3193, 1974). The development of a Ludox density gradient procedure has permitted preparation of large quantities of synchronous cells. The sedimentation coefficients of the envelope-associated nucleoids of stalked and swarmer cells, prepared under conditions of equivalent cell lysis, were 3,000S and greater than 6,000S respectively. Small differences in the relative amounts of deoxyribonucleic acid, ribonucleic acid, and protein in stalked and swarmer cell envelope-associated nucleoids could not account for the large differences in sedimentation behavior. These characteristic sedimentation coefficients were retained in mixing experiments.
通过对T. 科恩伯格等人(《美国国家科学院院刊》71:3189 - 3193, 1974年)的实验方法进行改进,从新月柄杆菌中分离出了与包膜相关的类核体。卢多克斯密度梯度法的发展使得大量同步细胞的制备成为可能。在等效细胞裂解条件下制备的柄细胞和游动细胞的与包膜相关的类核体的沉降系数分别为3000S和大于6000S。柄细胞和游动细胞的与包膜相关的类核体中脱氧核糖核酸、核糖核酸和蛋白质的相对含量的微小差异并不能解释沉降行为上的巨大差异。在混合实验中,这些特征性的沉降系数得以保留。