Isolation and characterization of flagellar filaments from Bacillus cereus ATCC 14579

被引:7
|
作者
Tagawa, Yuichi [1 ]
机构
[1] NARO, Natl Inst Anim Hlth, Tsukuba, Ibaraki 3050856, Japan
来源
ANTONIE VAN LEEUWENHOEK INTERNATIONAL JOURNAL OF GENERAL AND MOLECULAR MICROBIOLOGY | 2014年 / 106卷 / 06期
关键词
Bacillus cereus; Flagellar filament; Flagellin; Flagellin-specific antibody; H-ANTIGEN PROTEIN; LISTERIA-MONOCYTOGENES; SEQUENCE DIVERSITY; THURINGIENSIS; IDENTIFICATION; INVOLVEMENT; MOTILITY; GLYCOSYLATION; ANTHRACIS; CLONING;
D O I
10.1007/s10482-014-0285-2
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Isolated flagellar filaments from the type strain of Bacillus cereus, ATCC 14579, were shown to consist of 34, 32 and 31 kDa proteins in similar proportions as judged by band intensities on sodium dodecyl sulfate-polyacrylamide gel electrophoresis. The N-terminal amino acid sequences of these three proteins of strain ATCC 14579 were identical with the deduced sequences of three flagellin genes BC1657, BC1658 and BC1659 in the whole genome sequence. Strain ATCC 14579 was classified into serotype T2 by a flagellar serotyping scheme for B. cereus strains that are untypeable into known flagellar serotypes H1 to H23. Flagellar filaments from a reference strain of serotype T2 contained two protein bands at 34 and 32 kDa, but a single protein band at 39 kDa was detected in flagellar filaments of a reference strain of serotype H1. Two murine monoclonal antibodies, 1A5 and 2A5, which recognize both the 34 and 32 kDa flagellins and a single flagellin of 32 kDa, respectively, were specifically reactive with B. cereus strains ATCC 14579 and serotype T2 in whole-cell ELISA and bacterial motility inhibition tests. In immunoelectron microscopy with monoclonal antibodies 1A5 and 2A5, colloidal gold spheres were shown to localize almost evenly over the entire part of flagellar filaments. Since strain ATCC 14579, and presumably strain serotype T2, are unusual among B. cereus strains in possessing multiple genes that encode flagellin subunits, a possible unique mechanism may contribute to assembly of multiple flagellin subunits into the filament over its entire length.
引用
收藏
页码:1157 / 1165
页数:9
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