TY - JOUR
T1 - Identification of structural genes for Clostridium botulinum type C neurotoxin-converting phage particles
AU - Hwang, Hyun Jung
AU - Lee, Jae Chul
AU - Yamamoto, Yumiko
AU - Sarker, Mahfuzur R.
AU - Tsuchiya, Tomofusa
AU - Oguma, Keiji
N1 - Copyright:
Copyright 2009 Elsevier B.V., All rights reserved.
PY - 2007/5
Y1 - 2007/5
N2 - The structural genes for strain C-Stockholm (c-st) phage particles, a representative type C toxin-converting phage of Clostridium botulinum, have been determined. First, by determining the N-terminal amino acid sequences of sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) bands of c-st phage particles, it became clear that four proteins, 14, 25, 32 and 42 kDa, are the products of the ORFs, cst166, cst165, cst160 and cst164, respectively, of the c-st phage genome. The Western blot analyses reacting these phage bands with an antiphage serum prepared previously indicated that the products of cst165 and cst160 are the main proteins of the phage particles. Then, six candidates for the phage structural proteins, including cst165 and cst160 gene products, were prepared as recombinant proteins. Also, the protein corresponding to the cst164 gene product was excised from SDS-PAGE gels. The antibodies against these seven proteins were prepared in rabbits, and finally, the reaction of these antibodies to the c-st phage particles was analyzed by electron microscopy. It was concluded that a sheath protein and a head protein of the c-st phage are the products of genes cst160 and cst165, respectively, and that these two proteins are conserved in the other three converting phages, but not in the nonconverting phage.
AB - The structural genes for strain C-Stockholm (c-st) phage particles, a representative type C toxin-converting phage of Clostridium botulinum, have been determined. First, by determining the N-terminal amino acid sequences of sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) bands of c-st phage particles, it became clear that four proteins, 14, 25, 32 and 42 kDa, are the products of the ORFs, cst166, cst165, cst160 and cst164, respectively, of the c-st phage genome. The Western blot analyses reacting these phage bands with an antiphage serum prepared previously indicated that the products of cst165 and cst160 are the main proteins of the phage particles. Then, six candidates for the phage structural proteins, including cst165 and cst160 gene products, were prepared as recombinant proteins. Also, the protein corresponding to the cst164 gene product was excised from SDS-PAGE gels. The antibodies against these seven proteins were prepared in rabbits, and finally, the reaction of these antibodies to the c-st phage particles was analyzed by electron microscopy. It was concluded that a sheath protein and a head protein of the c-st phage are the products of genes cst160 and cst165, respectively, and that these two proteins are conserved in the other three converting phages, but not in the nonconverting phage.
KW - Botulinum toxin
KW - Clostridium botulinum
KW - Immunoelectron microscopy
KW - Phage
KW - Phage conversion
UR - http://www.scopus.com/inward/record.url?scp=34247117950&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=34247117950&partnerID=8YFLogxK
U2 - 10.1111/j.1574-6968.2007.00653.x
DO - 10.1111/j.1574-6968.2007.00653.x
M3 - Article
C2 - 17302935
AN - SCOPUS:34247117950
SN - 0378-1097
VL - 270
SP - 82
EP - 89
JO - FEMS Microbiology Letters
JF - FEMS Microbiology Letters
IS - 1
ER -