TY - JOUR
T1 - Subcellular distribution of Plp-40, a lipoprotein in a serotype A strain of Pasteurella multocida
AU - Nsofor, Margaret N.
AU - Ryals, Phillip E.
AU - Champlin, Franklin R.
N1 - Funding Information:
The authors are grateful to Dr. Masatoshi Inukai for generously providing the globomycin used in this investigation. We acknowledge Dr. M.M. Wade for her participation in discussions of segments of this research. Portions of this work were supported by Sigma Xi Grants-in-aid of research to Margaret N. Nsofor.
PY - 2006/8
Y1 - 2006/8
N2 - A 40-kDa lipoprotein (Plp-40) is expressed by serotype A strains of Pasteurella multocida in amounts which correlate with the amount of capsular material present. We hypothesized that Plp-40 is exposed at the outer surface of the outer membrane (OM) of the cell and is associated with the serotype A exopolysaccharide material. The objectives of the present study were to confirm the lipoprotein nature of Plp-40 and to determine its subcellular location. Plp-40 maturation was shown to be sensitive to globomycin, thereby confirming it to be a bacterial lipoprotein. Plp-40 was shown to be present in the OM fractions of P. multocida obtained by both sarkosyl extraction and sucrose density gradient centrifugation, as well as in capsule fractions obtained by either hyaluronidase treatment or warm buffer extraction. [3H]palmitic acid-labeled Plp-40 could be removed from the surface of whole cells by exposure to proteinase K. Autoradiography of 125I-labeled cell surface proteins exhibited a 40-kDa band that was prominent in capsulated strains and greatly diminished in a noncapsulated strain. These results support the hypothesis that Plp-40 is a lipid-modified OM protein, which is exposed on the outer cell surface and is likely associated with serotype A extracellular polysaccharide.
AB - A 40-kDa lipoprotein (Plp-40) is expressed by serotype A strains of Pasteurella multocida in amounts which correlate with the amount of capsular material present. We hypothesized that Plp-40 is exposed at the outer surface of the outer membrane (OM) of the cell and is associated with the serotype A exopolysaccharide material. The objectives of the present study were to confirm the lipoprotein nature of Plp-40 and to determine its subcellular location. Plp-40 maturation was shown to be sensitive to globomycin, thereby confirming it to be a bacterial lipoprotein. Plp-40 was shown to be present in the OM fractions of P. multocida obtained by both sarkosyl extraction and sucrose density gradient centrifugation, as well as in capsule fractions obtained by either hyaluronidase treatment or warm buffer extraction. [3H]palmitic acid-labeled Plp-40 could be removed from the surface of whole cells by exposure to proteinase K. Autoradiography of 125I-labeled cell surface proteins exhibited a 40-kDa band that was prominent in capsulated strains and greatly diminished in a noncapsulated strain. These results support the hypothesis that Plp-40 is a lipid-modified OM protein, which is exposed on the outer cell surface and is likely associated with serotype A extracellular polysaccharide.
KW - Capsule
KW - Cell envelope
KW - Outer membrane lipoprotein
KW - Pasteurella multocida
UR - http://www.scopus.com/inward/record.url?scp=33745280964&partnerID=8YFLogxK
U2 - 10.1016/j.bbagen.2006.03.004
DO - 10.1016/j.bbagen.2006.03.004
M3 - Article
C2 - 16735091
AN - SCOPUS:33745280964
SN - 0304-4165
VL - 1760
SP - 1160
EP - 1166
JO - Biochimica et Biophysica Acta - General Subjects
JF - Biochimica et Biophysica Acta - General Subjects
IS - 8
ER -