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. 1990 May;56(5):1235–1244. doi: 10.1128/aem.56.5.1235-1244.1990

Regulation and distribution of Fibrobacter succinogenes subsp. succinogenes S85 endoglucanases.

M McGavin 1, J Lam 1, C W Forsberg 1
PMCID: PMC184389  PMID: 2339882

Abstract

The distribution of endoglucanase activities in cultures of Fibrobacter succinogenes subsp. succinogenes S85 grown on different carbon sources was examined by a variety of biochemical and immunological techniques. Total culture endoglucanase activity was primarily cell associated and was expressed constitutively, although synthesis of endoglucanase 1 (EG1) was repressed by cellobiose. Western immunoblotting showed that EG1 and EG3 were released into the culture fluid during growth, while EG2 remained largely associated with the cell. Subcellular localization showed low endoglucanase activity in the periplasmic fraction and similar, high levels in the cytoplasmic and membrane fractions. Western immunoblotting showed that EG2 was absent from the periplasmic fraction. Data from immunoelectron microscopy with either polyclonal or monoclonal antibody to EG2 revealed a high density of gold labeling at sites where there was a disruption in the regular features of the cell surface, such as in blebbing or physical tearing of the membrane. When cells were grown on cellulose, there was a high density of labeling on the cellulose but not on the cells, indicating that EG2 has limited exposure at the cell surface. On the basis of these data, export of enzymes from their intracellular locations appears to occur via three different mechanisms: a specific secretory pathway independent of cellulose, a secretory mechanism which is mediated by contact with cellulose, and a generalized blebbing process that occurs irrespective of the carbon source.

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Selected References

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  1. Akin D. E. Ultrastructure of rumen bacterial attachment to forage cell walls. Appl Environ Microbiol. 1976 Apr;31(4):562–568. doi: 10.1128/aem.31.4.562-568.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bayer E. A., Kenig R., Lamed R. Adherence of Clostridium thermocellum to cellulose. J Bacteriol. 1983 Nov;156(2):818–827. doi: 10.1128/jb.156.2.818-827.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bayer E. A., Lamed R. Ultrastructure of the cell surface cellulosome of Clostridium thermocellum and its interaction with cellulose. J Bacteriol. 1986 Sep;167(3):828–836. doi: 10.1128/jb.167.3.828-836.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Bradford M. M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976 May 7;72:248–254. doi: 10.1006/abio.1976.9999. [DOI] [PubMed] [Google Scholar]
  5. Breuil C., Kushner D. J. Cellulase induction and the use of cellulose as a preferred growth substrate by Cellvibrio gilvus. Can J Microbiol. 1976 Dec;22(12):1776–1781. doi: 10.1139/m76-264. [DOI] [PubMed] [Google Scholar]
  6. Forsberg C. W., Beveridge T. J., Hellstrom A. Cellulase and Xylanase Release from Bacteroides succinogenes and Its Importance in the Rumen Environment. Appl Environ Microbiol. 1981 Nov;42(5):886–896. doi: 10.1128/aem.42.5.886-896.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Fusee M. C., Leatherwood J. M. Regulation of cellulase from Ruminococcus. Can J Microbiol. 1972 Mar;18(3):347–353. doi: 10.1139/m72-053. [DOI] [PubMed] [Google Scholar]
  8. Gawthorne J. M. Extracellular carbohydrase complex from rumen contents. Ann Rech Vet. 1979;10(2-3):249–250. [PubMed] [Google Scholar]
  9. Gong J., Forsberg C. W. Factors affecting adhesion of Fibrobacter succinogenes subsp. succinogenes S85 and adherence-defective mutants to cellulose. Appl Environ Microbiol. 1989 Dec;55(12):3039–3044. doi: 10.1128/aem.55.12.3039-3044.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Groleau D., Forsberg C. W. Cellulolytic activity of the rumen bacterium Bacteroides succinogenes. Can J Microbiol. 1981 May;27(5):517–530. doi: 10.1139/m81-077. [DOI] [PubMed] [Google Scholar]
  11. Groleau D., Forsberg C. W. Partial characterization of the extracellular carboxymethylcellulase activity produced by the rumen bacterium Bacteroides succinogenes. Can J Microbiol. 1983 May;29(5):504–517. doi: 10.1139/m83-080. [DOI] [PubMed] [Google Scholar]
  12. HALLIWELL G., BRYANT M. P. THE CELLULOLYTIC ACTIVITY OF PURE STRAINS OF BACTERIA FROM THE RUMEN OF CATTLE. J Gen Microbiol. 1963 Sep;32:441–448. doi: 10.1099/00221287-32-3-441. [DOI] [PubMed] [Google Scholar]
  13. HALLIWELL G. Cellulolysis by rumen micro-organisms. J Gen Microbiol. 1957 Aug;17(1):153–165. doi: 10.1099/00221287-17-1-153. [DOI] [PubMed] [Google Scholar]
  14. Hiltner P., Dehority B. A. Effect of soluble carbohydrates on digestion of cellulose by pure cultures of rumen bacteria. Appl Environ Microbiol. 1983 Sep;46(3):642–648. doi: 10.1128/aem.46.3.642-648.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Hirst T. R., Welch R. A. Mechanisms for secretion of extracellular proteins by gram-negative bacteria. Trends Biochem Sci. 1988 Jul;13(7):265–269. doi: 10.1016/0968-0004(88)90160-0. [DOI] [PubMed] [Google Scholar]
  16. Huang L., Forsberg C. W. Cellulose digestion and cellulase regulation and distribution in Fibrobacter succinogenes subsp. succinogenes S85. Appl Environ Microbiol. 1990 May;56(5):1221–1228. doi: 10.1128/aem.56.5.1221-1228.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Huang L., Forsberg C. W. Isolation of a Cellodextrinase from Bacteroides succinogenes. Appl Environ Microbiol. 1987 May;53(5):1034–1041. doi: 10.1128/aem.53.5.1034-1041.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Huang L., Forsberg C. W. Purification and Comparison of the Periplasmic and Extracellular Forms of the Cellodextrinase from Bacteroides succinogenes. Appl Environ Microbiol. 1988 Jun;54(6):1488–1493. doi: 10.1128/aem.54.6.1488-1493.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Huang L., Forsberg C. W., Thomas D. Y. Purification and characterization of a chloride-stimulated cellobiosidase from Bacteroides succinogenes S85. J Bacteriol. 1988 Jul;170(7):2923–2932. doi: 10.1128/jb.170.7.2923-2932.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Huang L., McGavin M., Forsberg C. W., Lam J. S., Cheng K. J. Antigenic nature of the chloride-stimulated cellobiosidase and other cellulases of Fibrobacter succinogenes subsp. succinogenes S85 and related fresh isolates. Appl Environ Microbiol. 1990 May;56(5):1229–1234. doi: 10.1128/aem.56.5.1229-1234.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Hungate R. E. Studies on Cellulose Fermentation: III. The Culture and Isolation for Cellulose-decomposing Bacteria from the Rumen of Cattle. J Bacteriol. 1947 May;53(5):631–645. doi: 10.1128/jb.53.5.631-645.1947. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
  23. Lamed R., Naimark J., Morgenstern E., Bayer E. A. Specialized cell surface structures in cellulolytic bacteria. J Bacteriol. 1987 Aug;169(8):3792–3800. doi: 10.1128/jb.169.8.3792-3800.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Lamed R., Setter E., Bayer E. A. Characterization of a cellulose-binding, cellulase-containing complex in Clostridium thermocellum. J Bacteriol. 1983 Nov;156(2):828–836. doi: 10.1128/jb.156.2.828-836.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Lin E., Wilson D. B. Regulation of beta-1,4-Endoglucanase Synthesis in Thermomonospora fusca. Appl Environ Microbiol. 1987 Jun;53(6):1352–1357. doi: 10.1128/aem.53.6.1352-1357.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. MALAMY M., HORECKER B. L. The localization of alkaline phosphatase in E. coli K12. Biochem Biophys Res Commun. 1961 Jun 2;5:104–108. doi: 10.1016/0006-291x(61)90020-1. [DOI] [PubMed] [Google Scholar]
  27. McGavin M. J., Forsberg C. W., Crosby B., Bell A. W., Dignard D., Thomas D. Y. Structure of the cel-3 gene from Fibrobacter succinogenes S85 and characteristics of the encoded gene product, endoglucanase 3. J Bacteriol. 1989 Oct;171(10):5587–5595. doi: 10.1128/jb.171.10.5587-5595.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. McGavin M., Forsberg C. W. Catalytic and substrate-binding domains of endoglucanase 2 from Bacteroides succinogenes. J Bacteriol. 1989 Jun;171(6):3310–3315. doi: 10.1128/jb.171.6.3310-3315.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. McGavin M., Forsberg C. W. Isolation and characterization of endoglucanases 1 and 2 from Bacteroides succinogenes S85. J Bacteriol. 1988 Jul;170(7):2914–2922. doi: 10.1128/jb.170.7.2914-2922.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Moreno J. D., Bayer R. The limits of the ledger in public health promotion. Hastings Cent Rep. 1985 Dec;15(6):37–41. [PubMed] [Google Scholar]
  31. Neu H. C., Heppel L. A. The release of enzymes from Escherichia coli by osmotic shock and during the formation of spheroplasts. J Biol Chem. 1965 Sep;240(9):3685–3692. [PubMed] [Google Scholar]
  32. Ng T. K., Weimer T. K., Zeikus J. G. Cellulolytic and physiological properties of Clostridium thermocellum. Arch Microbiol. 1977 Jul 26;114(1):1–7. doi: 10.1007/BF00429622. [DOI] [PubMed] [Google Scholar]
  33. Olmsted J. B. Affinity purification of antibodies from diazotized paper blots of heterogeneous protein samples. J Biol Chem. 1981 Dec 10;256(23):11955–11957. [PubMed] [Google Scholar]
  34. Pugsley A. P., Chapon C., Schwartz M. Extracellular pullulanase of Klebsiella pneumoniae is a lipoprotein. J Bacteriol. 1986 Jun;166(3):1083–1088. doi: 10.1128/jb.166.3.1083-1088.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. REYNOLDS E. S. The use of lead citrate at high pH as an electron-opaque stain in electron microscopy. J Cell Biol. 1963 Apr;17:208–212. doi: 10.1083/jcb.17.1.208. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. SCOTT H. W., DEHORITY B. A. VITAMIN REQUIREMENTS OF SEVERAL CELLULOLYTIC RUMEN BACTERIA. J Bacteriol. 1965 May;89:1169–1175. doi: 10.1128/jb.89.5.1169-1175.1965. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Smith W. R., Yu I., Hungate R. E. Factors affecting cellulolysis by Ruminococcus albus. J Bacteriol. 1973 May;114(2):729–737. doi: 10.1128/jb.114.2.729-737.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Stewart B. J., Leatherwood J. M. Derepressed synthesis of cellulase by Cellulomonas. J Bacteriol. 1976 Nov;128(2):609–615. doi: 10.1128/jb.128.2.609-615.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Stoppok W., Rapp P., Wagner F. Formation, Location, and Regulation of Endo-1,4-beta-Glucanases and beta-Glucosidases from Cellulomonas uda. Appl Environ Microbiol. 1982 Jul;44(1):44–53. doi: 10.1128/aem.44.1.44-53.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Thompson S. S., Naidu Y. M., Pestka J. J. Ultrastructural localization of an extracellular protease in Pseudomonas fragi by using the peroxidase-antiperoxidase reaction. Appl Environ Microbiol. 1985 Oct;50(4):1038–1042. doi: 10.1128/aem.50.4.1038-1042.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. 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]
  42. Wood W. E., Neubauer D. G., Stutzenberger F. J. Cyclic AMP levels during induction and repression of cellulase biosynthesis in Thermomonospora curvata. J Bacteriol. 1984 Dec;160(3):1047–1054. doi: 10.1128/jb.160.3.1047-1054.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. Wu H. C., Tokunaga M. Biogenesis of lipoproteins in bacteria. Curr Top Microbiol Immunol. 1986;125:127–157. doi: 10.1007/978-3-642-71251-7_9. [DOI] [PubMed] [Google Scholar]
  44. d'Enfert C., Chapon C., Pugsley A. P. Export and secretion of the lipoprotein pullulanase by Klebsiella pneumoniae. Mol Microbiol. 1987 Jul;1(1):107–116. doi: 10.1111/j.1365-2958.1987.tb00534.x. [DOI] [PubMed] [Google Scholar]

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