Abstract
A nonpigmented mutant of Porphyromonas gingivalis was constructed by using transposon mutagenesis. The mutant possessed the transposon DNA at the novel gene porR. Gene targeted mutagenesis revealed that porR was responsible for pigmentation. The porR gene shared similarities with genes of the degT family, the products of which are now considered to be transaminases involved in biosynthesis of sugar portions of cell-surface polysaccharides and aminoglycosides. The porR mutant showed a pleiotropic phenotype: delayed maturation of fimbrillin, preferential presence of Rgp and Kgp proteinases in culture supernatants, and no haemagglutination. The porR mutant had altered phenol extractable polysaccharide compared to the porR(+) sibling strain. A mAb, 1B5, that reacts with sugar portions of P. gingivalis cell surface polysaccharide and membrane-type Rgp proteinase showed no reaction with the cell lysates of the porR mutant. These results indicate that porR is involved in biosynthesis of cell surface polysaccharide that may function as an anchorage for Rgp, Kgp, haemagglutinins and the haemoglobin receptor protein.
MeSH Terms
Adhesins, Bacterial/metabolism
Amino Acid Sequence
Binding Sites
Chromosomes, Bacterial/genetics
Cysteine Endopeptidases/metabolism
Gingipain Cysteine Endopeptidases
Hemagglutination Tests
Hemagglutinins/metabolism
Molecular Sequence Data
Mutagenesis
Mutagenesis, Insertional
Phenotype
Pigmentation/genetics
Polysaccharides, Bacterial/metabolism
Porphyromonas gingivalis/genetics,pathogenicity
Restriction Mapping
Reverse Transcriptase Polymerase Chain Reaction
Sequence Alignment
Sequence Homology, Amino Acid
Transaminases/chemistry,genetics
Chemicals
Adhesins, Bacterial
Gingipain Cysteine Endopeptidases
Hemagglutinins
Polysaccharides, Bacterial
Transaminases
Cysteine Endopeptidases
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Shoji Mikio
Departments of Oral Infectious Diseases and Immunology1, Endodontology and Operative Dentistry2 and Pharmacology3, Faculty of Dental Science, Kyushu University, Fukuoka812-8582, Japan.
Ratnayake Dinath B
Departments of Oral Infectious Diseases and Immunology1, Endodontology and Operative Dentistry2 and Pharmacology3, Faculty of Dental Science, Kyushu University, Fukuoka812-8582, Japan.
Shi Yixin
Departments of Oral Infectious Diseases and Immunology1, Endodontology and Operative Dentistry2 and Pharmacology3, Faculty of Dental Science, Kyushu University, Fukuoka812-8582, Japan.
Kadowaki Tomoko
Departments of Oral Infectious Diseases and Immunology1, Endodontology and Operative Dentistry2 and Pharmacology3, Faculty of Dental Science, Kyushu University, Fukuoka812-8582, Japan.
Yamamoto Kenji
Departments of Oral Infectious Diseases and Immunology1, Endodontology and Operative Dentistry2 and Pharmacology3, Faculty of Dental Science, Kyushu University, Fukuoka812-8582, Japan.
Yoshimura Fuminobu
Department of Microbiology, School of Dentistry, Aichi-Gakuin University, Nagoya464-8650, Japan4.
Akamine Akifumi
Departments of Oral Infectious Diseases and Immunology1, Endodontology and Operative Dentistry2 and Pharmacology3, Faculty of Dental Science, Kyushu University, Fukuoka812-8582, Japan.
Curtis Michael A
Department of Medical Microbiology, Division of Molecular Pathology Infection and Immunity, St Bartholomew's and the Royal London School of Medicine and Dentistry, London E1 2AA, UK5.
Nakayama Koji
Department of Microbiology, School of Dentistry, Nagasaki University, Nagasaki 852-8588, Japan6.