OUTER-MEMBRANE GRAM-NEGATIVE BACTERIA .20. IDENTIFICATION OF THE PROTEIN PRODUCING TRANSMEMBRANE DIFFUSION PORES IN THE OUTER-MEMBRANE OF PSEUDOMONAS-AERUGINOSA PA01

被引:128
作者
HANCOCK, REW [1 ]
DECAD, GM [1 ]
NIKAIDO, H [1 ]
机构
[1] UNIV CALIF BERKELEY,DEPT BACTERIOL & IMMUNOL,BERKELEY,CA 94720
关键词
(Pseudomonas aeruginosa; Outer membrane); Membrane protein; Permeability; Porin; Reconstitution;
D O I
10.1016/0005-2736(79)90373-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The outer membrane of Pseudomonas aeruginosa PA01 is permeable to saccharides of molecular weights lower than about 6000. Triton X-100/EDTA-soluble outer membrane proteins were fractionated by ion-exchange chromatography in the presence of Triton X-100 and EDTA, and the protein contents of the various fractions analysed by sodium dodecyl sulphate polyacrylamide gel electrophoresis. Each of the major protein bands present in the Triton X-100/EDTA soluble outer membrane was separated from one another. Adjacent fractions were pooled, concentrated and extensively dialyzed to reduce the Triton X-100 concentration. Vesicles were reconstituted from lipopolysaccharide, phospholipids and each of these dialyzed fractions, and examined for their ability to retain [14C]sucrose. Control experiments indicated that the residual levels of Triton X-100 remaining in the dialyzed fractions had no effect on the formation or permeability to saccharides of the reconstituted vesicles. It was concluded that a major outer membrane polypeptide with an apparent weight of 35 000 is a porin, responsible for the size-dependent permeability of the outer membrane. © 1979.
引用
收藏
页码:323 / 331
页数:9
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