Lane 1, 33277; lane 2, KDP164 (hbp35 insertion mutant); lane 3, KDP166 (hbp35 deletion mutant). (PPT 390 KB) Additional file 2: Preparation of the anti-HBP35-immunoreactive 27-kDa protein for PMF analysis. Immunoprecipitates of lysates of KDP164 (hbp35 insertion mutant) with anti-HBP35 antibody was analyzed by SDS-PAGE followed by staining with CBB (left)

or immunoblot analysis with anti-HBP35 antibody (right). A 27-kDa protein band on the gel indicated was subjected to PMF analysis. (PPT 222 KB) Additional file 3: Structures of the HBP35 protein GSK2118436 molecular weight and the hbp35 gene. A. Domain organization of HBP35 protein. HBP35 contains a signal peptide region, a thioredoxin domain and a C-terminal domain. B. The hbp35 gene loci in various buy BI-D1870 mutant strains. Mutated hbp35 genes of KDP164 (hbp35

insertion mutant), KDP168 (hbp35 [M115A] insertion mutant), KDP169 (hbp35 [M135A] insertion mutant) and KDP170 (hbp35 [M115A M135A] insertion mutant) were depicted. (PPT 170 KB) Additional file 4: N-terminal amino acid sequencing of the recombinant 27-kDa protein produced in an E. coli expressing the hbp35 gene. rHBP35 products, which were partially purified using a C-terminal histidine-tag, were analyzed by SDS-PAGE followed by staining with CBB (left) or immunoblot analysis with anti-HBP35 PF 2341066 antibody (right). The N-terminal amino acid sequence of the recombinant 27-kDa protein was determined Resveratrol by Edman sequencing, resulting in M135 as an N-terminal residue. (PPT 320 KB) Additional file 5: Bacterial strains and plasmids used in this study. (XLS 32 KB) Additional file 6: Oligonucleotides used in this study. (DOC 35 KB) References 1. Roper JM, Raux E, Brindley AA, Schubert HL, Gharbia SE, Shah HN, Warren MJ: The enigma of cobalamin (Vitamin B12) biosynthesis in Porphyromonas gingivalis . Identification and characterization of a functional corrin pathway. J Biol Chem 2000,275(51):40316–40323.PubMedCrossRef 2. Kusaba A, Ansai T, Akifusa S, Nakahigashi K, Taketani S, Inokuchi H, Takehara T: Cloning and expression of a Porphyromonas gingivalis gene for protoporphyrinogen oxidase by complementation of a hemG mutant of Escherichia

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