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. 1992 Jan;174(1):309–314. doi: 10.1128/jb.174.1.309-314.1992

Lamina, a novel multicellular form of Methanosarcina mazei S-6.

L E Mayerhofer 1, A J Macario 1, E C de Macario 1
PMCID: PMC205710  PMID: 1370285

Abstract

A novel multicellular form of Methanosarcina mazei S-6 is described. It was termed lamina, and it formed during the exponential growth phase when packets or single cells were grown in 40 mM trimethylamine and a total concentration of 8.3 to 15.6 mM Ca2+ and/or Mg2+, in cultures that were not shaken. A distinct molecular event represented by the increment in expression and a spatial redistribution of an antigen during lamina formation is documented.

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Selected References

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  1. Boone D. R., Mah R. A. Effects of Calcium, Magnesium, pH, and Extent of Growth on the Morphology of Methanosarcina mazei S-6. Appl Environ Microbiol. 1987 Jul;53(7):1699–1700. doi: 10.1128/aem.53.7.1699-1700.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Boone D. R., Mathrani I. M., Mah R. A. H(2)-CO(2) Recirculation and pH Control for Growth of Methanogens in Mass Culture. Appl Environ Microbiol. 1987 May;53(5):946–948. doi: 10.1128/aem.53.5.946-948.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Boone D. R., Xun L. Effects of pH, Temperature, and Nutrients on Propionate Degradation by a Methanogenic Enrichment Culture. Appl Environ Microbiol. 1987 Jul;53(7):1589–1592. doi: 10.1128/aem.53.7.1589-1592.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Codogno P., Doyennette-Moyne M. A., Aubery M., Dieckhoff J., Lietzke R., Mannherz H. G. Polyclonal and monoclonal antibodies against chicken gizzard 5'-nucleotidase inhibit the spreading process of chicken embryonic fibroblasts on laminin substratum. Exp Cell Res. 1988 Feb;174(2):344–354. doi: 10.1016/0014-4827(88)90305-9. [DOI] [PubMed] [Google Scholar]
  5. Conway de Macario E., Macario A. J., Jovell R. J. Slide immunoenzymatic assay (SIA) in hybridoma technology. Methods Enzymol. 1986;121:509–525. doi: 10.1016/0076-6879(86)21051-4. [DOI] [PubMed] [Google Scholar]
  6. Edelman G. M. Morphoregulatory molecules. Biochemistry. 1988 May 17;27(10):3533–3543. doi: 10.1021/bi00410a001. [DOI] [PubMed] [Google Scholar]
  7. Gill J. S., Dworkin M. Cell surface antigens during submerged development of Myxococcus xanthus examined with monoclonal antibodies. J Bacteriol. 1986 Nov;168(2):505–511. doi: 10.1128/jb.168.2.505-511.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Harris J. E. Spontaneous Disaggregation of Methanosarcina mazei S-6 and Its Use in the Development of Genetic Techniques for Methanosarcina spp. Appl Environ Microbiol. 1987 Oct;53(10):2500–2504. doi: 10.1128/aem.53.10.2500-2504.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Liu Y., Boone D. R., Sleat R., Mah R. A. Methanosarcina mazei LYC, a New Methanogenic Isolate Which Produces a Disaggregating Enzyme. Appl Environ Microbiol. 1985 Mar;49(3):608–613. doi: 10.1128/aem.49.3.608-613.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Macario A. J., Conway de Macario E., Ney U., Schoberth S. M., Sahm H. Shifts in methanogenic subpopulations measured with antibody probes in a fixed-bed loop anaerobic bioreactor treating sulfite evaporator condensate. Appl Environ Microbiol. 1989 Aug;55(8):1996–2001. doi: 10.1128/aem.55.8.1996-2001.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Robinson R. W., Aldrich H. C., Hurst S. F., Bleiweis A. S. Role of the Cell Surface of Methanosarcina mazei in Cell Aggregation. Appl Environ Microbiol. 1985 Feb;49(2):321–327. doi: 10.1128/aem.49.2.321-327.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Robinson R. W. Life Cycles in the Methanogenic Archaebacterium Methanosarcina mazei. Appl Environ Microbiol. 1986 Jul;52(1):17–27. doi: 10.1128/aem.52.1.17-27.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Shimkets L. J. Control of morphogenesis in myxobacteria. Crit Rev Microbiol. 1987;14(3):195–227. doi: 10.3109/10408418709104439. [DOI] [PubMed] [Google Scholar]
  14. Sowers K. R., Gunsalus R. P. Adaptation for growth at various saline concentrations by the archaebacterium Methanosarcina thermophila. J Bacteriol. 1988 Feb;170(2):998–1002. doi: 10.1128/jb.170.2.998-1002.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Woese C. R. Bacterial evolution. Microbiol Rev. 1987 Jun;51(2):221–271. doi: 10.1128/mr.51.2.221-271.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Woese C. R., Kandler O., Wheelis M. L. Towards a natural system of organisms: proposal for the domains Archaea, Bacteria, and Eucarya. Proc Natl Acad Sci U S A. 1990 Jun;87(12):4576–4579. doi: 10.1073/pnas.87.12.4576. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Xun L. Y., Mah R. A., Boone D. R. Isolation and characterization of disaggregatase from Methanosarcina mazei LYC. Appl Environ Microbiol. 1990 Dec;56(12):3693–3698. doi: 10.1128/aem.56.12.3693-3698.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Xun L., Boone D. R., Mah R. A. Control of the Life Cycle of Methanosarcina mazei S-6 by Manipulation of Growth Conditions. Appl Environ Microbiol. 1988 Aug;54(8):2064–2068. doi: 10.1128/aem.54.8.2064-2068.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Zillig W., Palm P., Reiter W. D., Gropp F., Pühler G., Klenk H. P. Comparative evaluation of gene expression in archaebacteria. Eur J Biochem. 1988 May 2;173(3):473–482. doi: 10.1111/j.1432-1033.1988.tb14023.x. [DOI] [PubMed] [Google Scholar]

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