1) Streptococcus suis WcgA proteins are similar to the BpOF4_065

1). Streptococcus suis WcgA proteins are similar to the BpOF4_06575 protein predicted to be UDP-galactose phosphate transferase (71% identity) of Bacillus pseudofirmus OF4 (accession number: NC_013791). The initial sugar of the repeat unit is also the donor sugar in the polymerization of the repeat units. The specificity of the Wzy polymerase determines the other component of the CPS linkage (Bentley et al., 2006). The Wzy polymerase is quite different in the 15 serotypes. There are five polymerase HGs associated with WchA, two with WciI, 5 with WcaJ and one with WcgA (Table 1). These associations

are mostly exclusive, with only one polymerase HG (HG39) associated with two HGs of initial transferases. In such cases, the linkages may involve the same acceptor sugar anomerism (α or β isomer) and the same or closely related donor sugar. Wzx flippase can transport the repeat unit across the cytoplasmic membrane after CPS polymerization. GS-1101 cell line Except for serotype 16, only one wzx gene is located in the S. suis cps locus. Two wzx genes (cps16N and cps16R) exist in the cps16 locus. cps16O is similar to transposase gene (83% identity) of

Streptococcus mutans at the nucleic acid level. cps16N may be inactivated in the transposition-like events caused by Cps16O transposase. In the serotype 1, 2, 14, 16 and 1/2 cps locus, all the flippases belong to HG7. Each Wzx protein may transport polysaccharides see more with a similar composition and/or structure (Liu et al., 1996). The composition and/or structure were predicted to be similar in the five serotypes. GTs are important enzymes that catalyze the attachment of sugars (donor) to an aglycone (acceptor) in CPS synthesis.

Ignoring initial glycosylphosphotransferase, GTs in all 15 cps loci fall into 38 HGs. Two to seven GTs exist in each cps locus (Table 1). The predicted function of each GT HG is listed in Table S1. A putative GT enhancer (wchJ) is located in serotype 1, 14, 16 and 25. The mechanism and substrate of these enhancers are unknown. Aminotransferase genes are present in the serotype 3, 4, 5, 7, 19 and 23 cps loci. Amino-sugars are important Mirabegron components of some bacterial capsules (Hofmann et al., 1985; Beynon et al., 1990; Flahaut et al., 2008). Aminotransferases can transfer amino groups to sugars or form amino linked amidically to the carboxyl group (Beynon et al., 1990). We predicted that the CPS of serotypes 3, 4, 5, 7, 19 and 23 should be amino-sugar. Twelve different putative HGs of acetyltransferase, which play an important role in CPS structure determination (Calix & Nahm, 2010), are present in the 15 cps locus. Five genes (neuA, B, C, D and sialyltransferase) involved in sialic acid synthesis exist in the serotype 1, 2, 14, 16 and 1/2 cps loci. Because the identities of the genes involved in sialic acid synthesis between serotype 16 and 2 are very low (Wang et al.

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