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. 1996 Oct;178(20):6043–6048. doi: 10.1128/jb.178.20.6043-6048.1996

Cyclic beta-(1,2)-glucan synthesis in Rhizobiaceae: roles of the 319-kilodalton protein intermediate.

O A Castro 1, A Zorreguieta 1, V Ielmini 1, G Vega 1, L Ielpi 1
PMCID: PMC178464  PMID: 8830704

Abstract

Cyclic beta-(1,2)-glucans are synthesized by members of the Rhizobiaceae family through protein-linked oligosaccharides as intermediates. The protein moiety is a large inner membrane molecule of about 319 kDa. In Agrobacterium tumefaciens and in Rhizobium meliloti the protein is termed ChvB and NdvB, respectively. Inner membranes of R. meliloti 102F34 and A. tumefaciens A348 were first incubated with UDP-[14C]Glc and then solubilized with Triton X-100 and analyzed by polyacrylamide gel electrophoresis under native conditions. A radioactive band corresponding to the 319-kDa protein was detected in both bacteria. Triton-solubilized inner membranes of A. tumefaciens were submitted to native electrophoresis and then assayed for oligosaccharide-protein intermediate formation in situ by incubating the gel with UDP-[14C]Glc. A [14C]glucose-labeled protein with an electrophoretic mobility identical to that corresponding to the 319-kDa [14C]glucan protein intermediate was detected. In addition, protein-linked radioactivity was partially chased when the gel was incubated with unlabeled UDP-Glc. A heterogeneous family of cyclic beta-(1,2)-glucans was formed upon incubation of the gel portion containing the 319-kDa protein intermediate with UDP-[14C]Glc. A protein with an electrophoretic behavior similar to the 319-kDa protein intermediate was "in gel" labeled by using Triton-solubilized inner membranes of an A. tumefaciens exoC mutant, which contains a protein intermediate without nascent glucan. These results indicate that initiation (protein glucosylation), elongation, and cyclization were catalyzed in situ. Therefore, the three enzymatic activities detected in situ reside in a unique protein component (i.e., cyclic beta-(1,2)-glucan synthase). It is suggested that the protein component is the 319-kDa protein intermediate, which might catalyze the overall cyclic beta-(1,2)-glucan synthesis.

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Selected References

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  1. Altabe S., Iñn de Iannino N., de Mendoza D., Ugalde R. A. Expression of the Agrobacterium tumefaciens chvB virulence region in Azospirillum spp. J Bacteriol. 1990 May;172(5):2563–2567. doi: 10.1128/jb.172.5.2563-2567.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Ardila F. J., Tandecarz J. S. Potato Tuber UDP-Glucose:Protein Transglucosylase Catalyzes Its Own Glucosylation. Plant Physiol. 1992 Aug;99(4):1342–1347. doi: 10.1104/pp.99.4.1342. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bhagwat A. A., Tully R. E., Keister D. L. Isolation and characterization of an ndvB locus from Rhizobium fredii. Mol Microbiol. 1992 Aug;6(15):2159–2165. doi: 10.1111/j.1365-2958.1992.tb01389.x. [DOI] [PubMed] [Google Scholar]
  4. Breedveld M. W., Hadley J. A., Miller K. J. A novel cyclic beta-1,2-glucan mutant of Rhizobium meliloti. J Bacteriol. 1995 Nov;177(22):6346–6351. doi: 10.1128/jb.177.22.6346-6351.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Cangelosi G. A., Hung L., Puvanesarajah V., Stacey G., Ozga D. A., Leigh J. A., Nester E. W. Common loci for Agrobacterium tumefaciens and Rhizobium meliloti exopolysaccharide synthesis and their roles in plant interactions. J Bacteriol. 1987 May;169(5):2086–2091. doi: 10.1128/jb.169.5.2086-2091.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Cangelosi G. A., Martinetti G., Leigh J. A., Lee C. C., Thienes C., Theines C., Nester E. W. Role for [corrected] Agrobacterium tumefaciens ChvA protein in export of beta-1,2-glucan. J Bacteriol. 1989 Mar;171(3):1609–1615. doi: 10.1128/jb.171.3.1609-1615.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Chamberlain J. P. Fluorographic detection of radioactivity in polyacrylamide gels with the water-soluble fluor, sodium salicylate. Anal Biochem. 1979 Sep 15;98(1):132–135. doi: 10.1016/0003-2697(79)90716-4. [DOI] [PubMed] [Google Scholar]
  8. 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]
  9. Douglas C. J., Staneloni R. J., Rubin R. A., Nester E. W. Identification and genetic analysis of an Agrobacterium tumefaciens chromosomal virulence region. J Bacteriol. 1985 Mar;161(3):850–860. doi: 10.1128/jb.161.3.850-860.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Geiger O., Weissborn A. C., Kennedy E. P. Biosynthesis and excretion of cyclic glucans by Rhizobium meliloti 1021. J Bacteriol. 1991 May;173(9):3021–3024. doi: 10.1128/jb.173.9.3021-3024.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Ielpi L., Couso R. O., Dankert M. A. Sequential assembly and polymerization of the polyprenol-linked pentasaccharide repeating unit of the xanthan polysaccharide in Xanthomonas campestris. J Bacteriol. 1993 May;175(9):2490–2500. doi: 10.1128/jb.175.9.2490-2500.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Ielpi L., Dylan T., Ditta G. S., Helinski D. R., Stanfield S. W. The ndvB locus of Rhizobium meliloti encodes a 319-kDa protein involved in the production of beta-(1----2)-glucan. J Biol Chem. 1990 Feb 15;265(5):2843–2851. [PubMed] [Google Scholar]
  13. Krisman C. R., Barengo R. A precursor of glycogen biosynthesis: alpha-1,4-glucan-protein. Eur J Biochem. 1975 Mar 3;52(1):117–123. doi: 10.1111/j.1432-1033.1975.tb03979.x. [DOI] [PubMed] [Google Scholar]
  14. Miller K. J., Gore R. S., Benesi A. J. Phosphoglycerol substituents present on the cyclic beta-1,2-glucans of Rhizobium meliloti 1021 are derived from phosphatidylglycerol. J Bacteriol. 1988 Oct;170(10):4569–4575. doi: 10.1128/jb.170.10.4569-4575.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Miller K. J., Reinhold V. N., Weissborn A. C., Kennedy E. P. Cyclic glucans produced by Agrobacterium tumefaciens are substituted with sn-1-phosphoglycerol residues. Biochim Biophys Acta. 1987 Jul 10;901(1):112–118. doi: 10.1016/0005-2736(87)90262-8. [DOI] [PubMed] [Google Scholar]
  16. Moreno S., Cardini C. E., Tandecarz J. S. alpha-Glucan synthesis on a protein primer, uridine diphosphoglucose: protein transglucosylase I. Separation from starch synthetase and phosphorylase and a study of its properties. Eur J Biochem. 1986 Jun 16;157(3):539–545. doi: 10.1111/j.1432-1033.1986.tb09700.x. [DOI] [PubMed] [Google Scholar]
  17. O'Connell K. P., Handelsman J. chvA locus may be involved in export of neutral cyclic beta-1,2-linked D-glucan from Agrobacterium tumefaciens. Mol Plant Microbe Interact. 1989 Jan-Feb;2(1):11–16. [PubMed] [Google Scholar]
  18. Osborn M. J., Munson R. Separation of the inner (cytoplasmic) and outer membranes of Gram-negative bacteria. Methods Enzymol. 1974;31:642–653. doi: 10.1016/0076-6879(74)31070-1. [DOI] [PubMed] [Google Scholar]
  19. Pitcher J., Smythe C., Campbell D. G., Cohen P. Identification of the 38-kDa subunit of rabbit skeletal muscle glycogen synthase as glycogenin. Eur J Biochem. 1987 Dec 15;169(3):497–502. doi: 10.1111/j.1432-1033.1987.tb13637.x. [DOI] [PubMed] [Google Scholar]
  20. Pitcher J., Smythe C., Cohen P. Glycogenin is the priming glucosyltransferase required for the initiation of glycogen biogenesis in rabbit skeletal muscle. Eur J Biochem. 1988 Sep 15;176(2):391–395. doi: 10.1111/j.1432-1033.1988.tb14294.x. [DOI] [PubMed] [Google Scholar]
  21. Smythe C., Caudwell F. B., Ferguson M., Cohen P. Isolation and structural analysis of a peptide containing the novel tyrosyl-glucose linkage in glycogenin. EMBO J. 1988 Sep;7(9):2681–2686. doi: 10.1002/j.1460-2075.1988.tb03121.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Stanfield S. W., Ielpi L., O'Brochta D., Helinski D. R., Ditta G. S. The ndvA gene product of Rhizobium meliloti is required for beta-(1----2)glucan production and has homology to the ATP-binding export protein HlyB. J Bacteriol. 1988 Aug;170(8):3523–3530. doi: 10.1128/jb.170.8.3523-3530.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Tolmasky M. E., Staneloni R. J., Leloir L. F. Lipid-bound saccharides in Rhizobium meliloti. J Biol Chem. 1982 Jun 25;257(12):6751–6757. [PubMed] [Google Scholar]
  24. Uttaro A. D., Cangelosi G. A., Geremia R. A., Nester E. W., Ugalde R. A. Biochemical characterization of avirulent exoC mutants of Agrobacterium tumefaciens. J Bacteriol. 1990 Mar;172(3):1640–1646. doi: 10.1128/jb.172.3.1640-1646.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Williamson G., Damani K., Devenney P., Faulds C. B., Morris V. J., Stevens B. J. Mechanism of action of cyclic beta-1,2-glucan synthetase from Agrobacterium tumefaciens: competition between cyclization and elongation reactions. J Bacteriol. 1992 Dec;174(24):7941–7947. doi: 10.1128/jb.174.24.7941-7947.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Zevenhuizen L. P., van Veldhuizen A., Fokkens R. H. Re-examination of cellular cyclic beta-1,2-glucans of Rhizobiaceae: distribution of ring sizes and degrees of glycerol-1-phosphate substitution. Antonie Van Leeuwenhoek. 1990 Apr;57(3):173–178. doi: 10.1007/BF00403952. [DOI] [PubMed] [Google Scholar]
  27. Zorreguieta A., Geremia R. A., Cavaignac S., Cangelosi G. A., Nester E. W., Ugalde R. A. Identification of the product of an Agrobacterium tumefaciens chromosomal virulence gene. Mol Plant Microbe Interact. 1988 Mar;1(3):121–127. doi: 10.1094/mpmi-1-121. [DOI] [PubMed] [Google Scholar]
  28. Zorreguieta A., Tolmasky M. E., Staneloni R. J. The enzymatic synthesis of beta 1-2 glucans. Arch Biochem Biophys. 1985 May 1;238(2):368–372. doi: 10.1016/0003-9861(85)90176-6. [DOI] [PubMed] [Google Scholar]
  29. Zorreguieta A., Ugalde R. A. Formation in Rhizobium and Agrobacterium spp. of a 235-kilodalton protein intermediate in beta-D(1-2) glucan synthesis. J Bacteriol. 1986 Sep;167(3):947–951. doi: 10.1128/jb.167.3.947-951.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Zorreguieta A., Ugalde R. A., Leloir L. F. An intermediate in cyclic beta 1-2 glucan biosynthesis. Biochem Biophys Res Commun. 1985 Jan 16;126(1):352–357. doi: 10.1016/0006-291x(85)90613-8. [DOI] [PubMed] [Google Scholar]
  31. de Iannino N. I., Ugalde R. A. Biochemical characterization of avirulent Agrobacterium tumefaciens chvA mutants: synthesis and excretion of beta-(1-2)glucan. J Bacteriol. 1989 May;171(5):2842–2849. doi: 10.1128/jb.171.5.2842-2849.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]

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