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. 1995 Oct;177(19):5411–5418. doi: 10.1128/jb.177.19.5411-5418.1995

Role of Rfe and RfbF in the initiation of biosynthesis of D-galactan I, the lipopolysaccharide O antigen from Klebsiella pneumoniae serotype O1.

B R Clarke 1, D Bronner 1, W J Keenleyside 1, W B Severn 1, J C Richards 1, C Whitfield 1
PMCID: PMC177345  PMID: 7559323

Abstract

The 6.6-kb rfb gene cluster from Klebsiella pneumoniae serotype O1 (rfbKpO1) contains six genes whose products are required for the biosynthesis of a lipopolysaccharide O antigen with the following repeating unit structure: -->3-beta-D-Galf-1-->3-alpha-D-Galp-1-->(D-galactan I). rfbFKpO1 is the last gene in the cluster, and its gene product is required for the initiation of D-galactan I synthesis. Escherichia coli K-12 strains expressing the RfbFKpO1 polypeptide contain dual galactopyranosyl and galactofuranosyl transferase activity. This activity modifies the host lipopolysaccharide core by adding the disaccharide beta-D-Galf-1-->3-alpha-D-Galp, representing a single repeating unit of D-galactan I. The formation of the lipopolysaccharide substituted either with the disaccharide or with authentic polymeric D-galactan I is dependent on the activity of the Rfe enzyme. Rfe (UDP-GlcpNAc::undecaprenylphosphate GlcpNAc-1-phosphate transferase) catalyzes the formation of the lipid-linked biosynthetic intermediate to which galactosyl residues are transferred during the initial steps of D-galactan I synthesis. The rfbFKpO1 gene comprises 1,131 nucleotides, and the predicted polypeptide consists of 373 amino acid residues with a predicted M(r) of 42,600. A polypeptide with an M(r) of 42,000 was evident in sodium dodecyl sulfate-polyacrylamide gels when rfbKpO1 was expressed behind the T7 promoter. The carboxy-terminal region of RfbFKpO1 shares similarity with the carboxy terminus of RfpB, a galactopyranosyl transferase which is involved in the synthesis of the type 1 O antigen of Shigella dysenteriae.

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Selected References

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  1. Alexander D. C., Valvano M. A. Role of the rfe gene in the biosynthesis of the Escherichia coli O7-specific lipopolysaccharide and other O-specific polysaccharides containing N-acetylglucosamine. J Bacteriol. 1994 Nov;176(22):7079–7084. doi: 10.1128/jb.176.22.7079-7084.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Altschul S. F., Gish W., Miller W., Myers E. W., Lipman D. J. Basic local alignment search tool. J Mol Biol. 1990 Oct 5;215(3):403–410. doi: 10.1016/S0022-2836(05)80360-2. [DOI] [PubMed] [Google Scholar]
  3. Aucken H. M., Oxley D., Wilkinson S. G. Structural and serological characterisation of an O-specific polysaccharide from Serratia plymuthica. FEMS Microbiol Lett. 1993 Aug 1;111(2-3):295–300. doi: 10.1111/j.1574-6968.1993.tb06401.x. [DOI] [PubMed] [Google Scholar]
  4. Bachmann B. J. Linkage map of Escherichia coli K-12, edition 8. Microbiol Rev. 1990 Jun;54(2):130–197. doi: 10.1128/mr.54.2.130-197.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Bronner D., Clarke B. R., Whitfield C. Identification of an ATP-binding cassette transport system required for translocation of lipopolysaccharide O-antigen side-chains across the cytoplasmic membrane of Klebsiella pneumoniae serotype O1. Mol Microbiol. 1994 Nov;14(3):505–519. doi: 10.1111/j.1365-2958.1994.tb02185.x. [DOI] [PubMed] [Google Scholar]
  6. Bronner D., Sieberth V., Pazzani C., Roberts I. S., Boulnois G. J., Jann B., Jann K. Expression of the capsular K5 polysaccharide of Escherichia coli: biochemical and electron microscopic analyses of mutants with defects in region 1 of the K5 gene cluster. J Bacteriol. 1993 Sep;175(18):5984–5992. doi: 10.1128/jb.175.18.5984-5992.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Clarke B. R., Whitfield C. Molecular cloning of the rfb region of Klebsiella pneumoniae serotype O1:K20: the rfb gene cluster is responsible for synthesis of the D-galactan I O polysaccharide. J Bacteriol. 1992 Jul;174(14):4614–4621. doi: 10.1128/jb.174.14.4614-4621.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. DeAngelis P. L., Weigel P. H. Immunochemical confirmation of the primary structure of streptococcal hyaluronan synthase and synthesis of high molecular weight product by the recombinant enzyme. Biochemistry. 1994 Aug 9;33(31):9033–9039. doi: 10.1021/bi00197a001. [DOI] [PubMed] [Google Scholar]
  9. Ditta G., Schmidhauser T., Yakobson E., Lu P., Liang X. W., Finlay D. R., Guiney D., Helinski D. R. Plasmids related to the broad host range vector, pRK290, useful for gene cloning and for monitoring gene expression. Plasmid. 1985 Mar;13(2):149–153. doi: 10.1016/0147-619x(85)90068-x. [DOI] [PubMed] [Google Scholar]
  10. Ditta G., Stanfield S., Corbin D., Helinski D. R. Broad host range DNA cloning system for gram-negative bacteria: construction of a gene bank of Rhizobium meliloti. Proc Natl Acad Sci U S A. 1980 Dec;77(12):7347–7351. doi: 10.1073/pnas.77.12.7347. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Dunn S. D. Effects of the modification of transfer buffer composition and the renaturation of proteins in gels on the recognition of proteins on Western blots by monoclonal antibodies. Anal Biochem. 1986 Aug 15;157(1):144–153. doi: 10.1016/0003-2697(86)90207-1. [DOI] [PubMed] [Google Scholar]
  12. Finke A., Bronner D., Nikolaev A. V., Jann B., Jann K. Biosynthesis of the Escherichia coli K5 polysaccharide, a representative of group II capsular polysaccharides: polymerization in vitro and characterization of the product. J Bacteriol. 1991 Jul;173(13):4088–4094. doi: 10.1128/jb.173.13.4088-4094.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Fält I. C., Schweda E. K., Weintraub A., Sturm S., Timmis K. N., Lindberg A. A. Expression of the Shigella dysenteriae type-1 lipopolysaccharide repeating unit in Escherichia coli K12/Shigella dysenteriae type-1 hybrids. Eur J Biochem. 1993 Apr 1;213(1):573–581. doi: 10.1111/j.1432-1033.1993.tb17796.x. [DOI] [PubMed] [Google Scholar]
  14. Göhmann S., Manning P. A., Alpert C. A., Walker M. J., Timmis K. N. Lipopolysaccharide O-antigen biosynthesis in Shigella dysenteriae serotype 1: analysis of the plasmid-carried rfp determinant. Microb Pathog. 1994 Jan;16(1):53–64. doi: 10.1006/mpat.1994.1005. [DOI] [PubMed] [Google Scholar]
  15. HAKOMORI S. A RAPID PERMETHYLATION OF GLYCOLIPID, AND POLYSACCHARIDE CATALYZED BY METHYLSULFINYL CARBANION IN DIMETHYL SULFOXIDE. J Biochem. 1964 Feb;55:205–208. [PubMed] [Google Scholar]
  16. Hitchcock P. J., Brown T. M. Morphological heterogeneity among Salmonella lipopolysaccharide chemotypes in silver-stained polyacrylamide gels. J Bacteriol. 1983 Apr;154(1):269–277. doi: 10.1128/jb.154.1.269-277.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Holst O., Zähringer U., Brade H., Zamojski A. Structural analysis of the heptose/hexose region of the lipopolysaccharide from Escherichia coli K-12 strain W3100. Carbohydr Res. 1991 Aug 20;215(2):323–335. doi: 10.1016/0008-6215(91)84031-9. [DOI] [PubMed] [Google Scholar]
  18. Jansson P. E., Lindberg A. A., Lindberg B., Wollin R. Structural studies on the hexose region of the core in lipopolysaccharides from Enterobacteriaceae. Eur J Biochem. 1981 Apr;115(3):571–577. doi: 10.1111/j.1432-1033.1981.tb06241.x. [DOI] [PubMed] [Google Scholar]
  19. Jiang X. M., Neal B., Santiago F., Lee S. J., Romana L. K., Reeves P. R. Structure and sequence of the rfb (O antigen) gene cluster of Salmonella serovar typhimurium (strain LT2). Mol Microbiol. 1991 Mar;5(3):695–713. doi: 10.1111/j.1365-2958.1991.tb00741.x. [DOI] [PubMed] [Google Scholar]
  20. Johnson K. G., Perry M. B. Improved techniques for the preparation of bacterial lipopolysaccharides. Can J Microbiol. 1976 Jan;22(1):29–34. doi: 10.1139/m76-004. [DOI] [PubMed] [Google Scholar]
  21. Kelly R. F., Severn W. B., Richards J. C., Perry M. B., MacLean L. L., Tomás J. M., Merino S., Whitfield C. Structural variation in the O-specific polysaccharides of Klebsiella pneumoniae serotype O1 and O8 lipopolysaccharide: evidence for clonal diversity in rfb genes. Mol Microbiol. 1993 Nov;10(3):615–625. doi: 10.1111/j.1365-2958.1993.tb00933.x. [DOI] [PubMed] [Google Scholar]
  22. Kido N., Torgov V. I., Sugiyama T., Uchiya K., Sugihara H., Komatsu T., Kato N., Jann K. Expression of the O9 polysaccharide of Escherichia coli: sequencing of the E. coli O9 rfb gene cluster, characterization of mannosyl transferases, and evidence for an ATP-binding cassette transport system. J Bacteriol. 1995 Apr;177(8):2178–2187. doi: 10.1128/jb.177.8.2178-2187.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Klena J. D., Ashford R. S., 2nd, Schnaitman C. A. Role of Escherichia coli K-12 rfa genes and the rfp gene of Shigella dysenteriae 1 in generation of lipopolysaccharide core heterogeneity and attachment of O antigen. J Bacteriol. 1992 Nov;174(22):7297–7307. doi: 10.1128/jb.174.22.7297-7307.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Klena J. D., Schnaitman C. A. Function of the rfb gene cluster and the rfe gene in the synthesis of O antigen by Shigella dysenteriae 1. Mol Microbiol. 1993 Jul;9(2):393–402. doi: 10.1111/j.1365-2958.1993.tb01700.x. [DOI] [PubMed] [Google Scholar]
  25. Kogan G., Haraguchi G., Hull S. I., Hull R. A., Shashkov A. S., Jann B., Jann K. Structural analysis of O4-reactive polysaccharides from recombinant Escherichia coli. Changes in the O-specific polysaccharide induced by cloning of the rfb genes. Eur J Biochem. 1993 May 15;214(1):259–265. doi: 10.1111/j.1432-1033.1993.tb17919.x. [DOI] [PubMed] [Google Scholar]
  26. Kol O., Wieruszeski J. M., Strecker G., Fournet B., Zalisz R., Smets P. Structure of the O-specific polysaccharide chain of Klebsiella pneumoniae O1K2 (NCTC 5055) lipopolysaccharide. A complementary elucidation. Carbohydr Res. 1992 Dec 15;236:339–344. doi: 10.1016/0008-6215(92)85028-x. [DOI] [PubMed] [Google Scholar]
  27. Kol O., Wieruszeski J. M., Strecker G., Montreuil J., Fournet B., Zalisz R., Smets P. Structure of the O-specific polysaccharide chain from Klebsiella pneumoniae O1K2 (NCTC 5055) lipopolysaccharide. Carbohydr Res. 1991 Sep 18;217:117–125. doi: 10.1016/0008-6215(91)84122-u. [DOI] [PubMed] [Google Scholar]
  28. Lidholt K., Fjelstad M., Jann K., Lindahl U. Substrate specificities of glycosyltransferases involved in formation of heparin precursor and E. coli K5 capsular polysaccharides. Carbohydr Res. 1994 Mar 4;255:87–101. doi: 10.1016/s0008-6215(00)90972-8. [DOI] [PubMed] [Google Scholar]
  29. Lidholt K., Weinke J. L., Kiser C. S., Lugemwa F. N., Bame K. J., Cheifetz S., Massagué J., Lindahl U., Esko J. D. A single mutation affects both N-acetylglucosaminyltransferase and glucuronosyltransferase activities in a Chinese hamster ovary cell mutant defective in heparan sulfate biosynthesis. Proc Natl Acad Sci U S A. 1992 Mar 15;89(6):2267–2271. doi: 10.1073/pnas.89.6.2267. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Lind T., Lindahl U., Lidholt K. Biosynthesis of heparin/heparan sulfate. Identification of a 70-kDa protein catalyzing both the D-glucuronosyl- and the N-acetyl-D-glucosaminyltransferase reactions. J Biol Chem. 1993 Oct 5;268(28):20705–20708. [PubMed] [Google Scholar]
  31. MacLean L. L., Whitfield C., Perry M. B. Characterization of the polysaccharide antigen of Klebsiella pneumoniae O:9 lipopolysaccharide. Carbohydr Res. 1993 Feb 1;239:325–328. doi: 10.1016/0008-6215(93)84231-t. [DOI] [PubMed] [Google Scholar]
  32. Meier-Dieter U., Barr K., Starman R., Hatch L., Rick P. D. Nucleotide sequence of the Escherichia coli rfe gene involved in the synthesis of enterobacterial common antigen. Molecular cloning of the rfe-rff gene cluster. J Biol Chem. 1992 Jan 15;267(2):746–753. [PubMed] [Google Scholar]
  33. Meier-Dieter U., Starman R., Barr K., Mayer H., Rick P. D. Biosynthesis of enterobacterial common antigen in Escherichia coli. Biochemical characterization of Tn10 insertion mutants defective in enterobacterial common antigen synthesis. J Biol Chem. 1990 Aug 15;265(23):13490–13497. [PubMed] [Google Scholar]
  34. Morona R., Mavris M., Fallarino A., Manning P. A. Characterization of the rfc region of Shigella flexneri. J Bacteriol. 1994 Feb;176(3):733–747. doi: 10.1128/jb.176.3.733-747.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Neuhard J., Thomassen E. Altered deoxyribonucleotide pools in P2 eductants of Escherichia coli K-12 due to deletion of the dcd gene. J Bacteriol. 1976 May;126(2):999–1001. doi: 10.1128/jb.126.2.999-1001.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Oxley D., Wilkinson S. G. Structures of neutral glycans isolated from the lipopolysaccharides of reference strains for Serratia marcescens serogroups O16 and O20. Carbohydr Res. 1989 Oct 31;193:241–248. doi: 10.1016/0008-6215(89)85122-5. [DOI] [PubMed] [Google Scholar]
  37. Pavelka M. S., Jr, Wright L. F., Silver R. P. Identification of two genes, kpsM and kpsT, in region 3 of the polysialic acid gene cluster of Escherichia coli K1. J Bacteriol. 1991 Aug;173(15):4603–4610. doi: 10.1128/jb.173.15.4603-4610.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Reeves P. Evolution of Salmonella O antigen variation by interspecific gene transfer on a large scale. Trends Genet. 1993 Jan;9(1):17–22. doi: 10.1016/0168-9525(93)90067-R. [DOI] [PubMed] [Google Scholar]
  39. Richards J. C., Leitch R. A. Elucidation of the structure of the Pasteurella haemolytica serotype T10 lipopolysaccharide O-antigen by n.m.r. spectroscopy. Carbohydr Res. 1989 Mar 15;186(2):275–286. doi: 10.1016/0008-6215(89)84041-8. [DOI] [PubMed] [Google Scholar]
  40. Rick P. D., Hubbard G. L., Barr K. Role of the rfe gene in the synthesis of the O8 antigen in Escherichia coli K-12. J Bacteriol. 1994 May;176(10):2877–2884. doi: 10.1128/jb.176.10.2877-2884.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Sanger F., Nicklen S., Coulson A. R. DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci U S A. 1977 Dec;74(12):5463–5467. doi: 10.1073/pnas.74.12.5463. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Sarvas M., Nikaido H. Biosynthesis of T1 antigen in Salmonella: origin of D-galactofuranose and D-ribofuranose residues. J Bacteriol. 1971 Mar;105(3):1063–1072. doi: 10.1128/jb.105.3.1063-1072.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. Schnaitman C. A., Austin E. A. Efficient incorporation of galactose into lipopolysaccharide by Escherichia coli K-12 strains with polar galE mutations. J Bacteriol. 1990 Sep;172(9):5511–5513. doi: 10.1128/jb.172.9.5511-5513.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  44. Smith A. N., Boulnois G. J., Roberts I. S. Molecular analysis of the Escherichia coli K5 kps locus: identification and characterization of an inner-membrane capsular polysaccharide transport system. Mol Microbiol. 1990 Nov;4(11):1863–1869. doi: 10.1111/j.1365-2958.1990.tb02035.x. [DOI] [PubMed] [Google Scholar]
  45. Stachel S. E., An G., Flores C., Nester E. W. A Tn3 lacZ transposon for the random generation of beta-galactosidase gene fusions: application to the analysis of gene expression in Agrobacterium. EMBO J. 1985 Apr;4(4):891–898. doi: 10.1002/j.1460-2075.1985.tb03715.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  46. Steenbergen S. M., Vimr E. R. Mechanism of polysialic acid chain elongation in Escherichia coli K1. Mol Microbiol. 1990 Apr;4(4):603–611. doi: 10.1111/j.1365-2958.1990.tb00629.x. [DOI] [PubMed] [Google Scholar]
  47. Steenbergen S. M., Wrona T. J., Vimr E. R. Functional analysis of the sialyltransferase complexes in Escherichia coli K1 and K92. J Bacteriol. 1992 Feb;174(4):1099–1108. doi: 10.1128/jb.174.4.1099-1108.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  48. Stevenson G., Neal B., Liu D., Hobbs M., Packer N. H., Batley M., Redmond J. W., Lindquist L., Reeves P. Structure of the O antigen of Escherichia coli K-12 and the sequence of its rfb gene cluster. J Bacteriol. 1994 Jul;176(13):4144–4156. doi: 10.1128/jb.176.13.4144-4156.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  49. Sturm S., Jann B., Jann K., Fortnagel P., Timmis K. N. Genetic and biochemical analysis of Shigella dysenteriae 1 O antigen polysaccharide biosynthesis in Escherichia coli K-12: 9 kb plasmid of S. dysenteriae 1 determines addition of a galactose residue to the lipopolysaccharide core. Microb Pathog. 1986 Jun;1(3):299–306. doi: 10.1016/0882-4010(86)90055-0. [DOI] [PubMed] [Google Scholar]
  50. Sturm S., Timmis K. N. Cloning of the rfb gene region of Shigella dysenteriae 1 and construction of an rfb-rfp gene cassette for the development of lipopolysaccharide-based live anti-dysentery vaccines. Microb Pathog. 1986 Jun;1(3):289–297. doi: 10.1016/0882-4010(86)90054-9. [DOI] [PubMed] [Google Scholar]
  51. Sugiyama T., Kido N., Komatsu T., Ohta M., Kato N. Expression of the cloned Escherichia coli O9 rfb gene in various mutant strains of Salmonella typhimurium. J Bacteriol. 1991 Jan;173(1):55–58. doi: 10.1128/jb.173.1.55-58.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  52. Szabo M., Bronner D., Whitfield C. Relationships between rfb gene clusters required for biosynthesis of identical D-galactose-containing O antigens in Klebsiella pneumoniae serotype O1 and Serratia marcescens serotype O16. J Bacteriol. 1995 Mar;177(6):1544–1553. doi: 10.1128/jb.177.6.1544-1553.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  53. Tabor S., Richardson C. C. A bacteriophage T7 RNA polymerase/promoter system for controlled exclusive expression of specific genes. Proc Natl Acad Sci U S A. 1985 Feb;82(4):1074–1078. doi: 10.1073/pnas.82.4.1074. [DOI] [PMC free article] [PubMed] [Google Scholar]
  54. Towbin H., Staehelin T., Gordon J. Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications. Proc Natl Acad Sci U S A. 1979 Sep;76(9):4350–4354. doi: 10.1073/pnas.76.9.4350. [DOI] [PMC free article] [PubMed] [Google Scholar]
  55. Tsai C. M., Frasch C. E. A sensitive silver stain for detecting lipopolysaccharides in polyacrylamide gels. Anal Biochem. 1982 Jan 1;119(1):115–119. doi: 10.1016/0003-2697(82)90673-x. [DOI] [PubMed] [Google Scholar]
  56. Vimr E. R., Bergstrom R., Steenbergen S. M., Boulnois G., Roberts I. Homology among Escherichia coli K1 and K92 polysialytransferases. J Bacteriol. 1992 Aug;174(15):5127–5131. doi: 10.1128/jb.174.15.5127-5131.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  57. Wang L., Reeves P. R. Involvement of the galactosyl-1-phosphate transferase encoded by the Salmonella enterica rfbP gene in O-antigen subunit processing. J Bacteriol. 1994 Jul;176(14):4348–4356. doi: 10.1128/jb.176.14.4348-4356.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  58. Whitfield C. Biosynthesis of lipopolysaccharide O antigens. Trends Microbiol. 1995 May;3(5):178–185. doi: 10.1016/s0966-842x(00)88917-9. [DOI] [PubMed] [Google Scholar]
  59. Whitfield C., Perry M. B., MacLean L. L., Yu S. H. Structural analysis of the O-antigen side chain polysaccharides in the lipopolysaccharides of Klebsiella serotypes O2(2a), O2(2a,2b), and O2(2a,2c). J Bacteriol. 1992 Aug;174(15):4913–4919. doi: 10.1128/jb.174.15.4913-4919.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  60. Whitfield C., Richards J. C., Perry M. B., Clarke B. R., MacLean L. L. Expression of two structurally distinct D-galactan O antigens in the lipopolysaccharide of Klebsiella pneumoniae serotype O1. J Bacteriol. 1991 Feb;173(4):1420–1431. doi: 10.1128/jb.173.4.1420-1431.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  61. Whitfield C., Valvano M. A. Biosynthesis and expression of cell-surface polysaccharides in gram-negative bacteria. Adv Microb Physiol. 1993;35:135–246. doi: 10.1016/s0065-2911(08)60099-5. [DOI] [PubMed] [Google Scholar]
  62. Yao Z., Valvano M. A. Genetic analysis of the O-specific lipopolysaccharide biosynthesis region (rfb) of Escherichia coli K-12 W3110: identification of genes that confer group 6 specificity to Shigella flexneri serotypes Y and 4a. J Bacteriol. 1994 Jul;176(13):4133–4143. doi: 10.1128/jb.176.13.4133-4143.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]

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