Previous Article | Next Article ![]()
Appl. Environ. Microbiol., May 1995, 1757-1762, Vol 61, No. 5
JE Wells, JB Russell, Y Shi and PJ Weimer
When glucose or cellobiose was provided as an energy source for Fibrobacter
succinogenes, there was a transient accumulation (as much as 0.4 mM hexose
equivalent) of cellobiose or cellotriose, respectively, in the growth
medium. Nongrowing cell suspensions converted cellobiose to cellotriose and
longer-chain cellodextrins, and in this case the total cellodextrin
concentration was as much as 20 mM (hexose equivalent). Because cell
extracts of glucose- or cellobiose- grown cells cleaved cellobioise and
cellotriose by phosphate-dependent reactions and glucose 1-phosphate was an
end product, it appeared that cellodextrins were being produced by a
reversible phosphorylase reaction. This conclusion was supported by the
observation that the ratio of cellodextrins to cellodextrins with one
greater hexose [n/(n + 1)] was approximately 4, a value similar to the
equilibrium constant (Keq) of cellobiose phosphorylase (J. K. Alexander, J.
Bacteriol. 81:903-910, 1961). When F. succinogenes was grown in a
cellobiose- limited chemostat, cellobiose and cellotriose could both be
detected, and the ratio of cellotriose to cellobiose was approximately 1 to
4. On the basis of these results, cellodextrin production is an equilibrium
(mass action) function and not just an artifact of energy-rich cultural
conditions. Cellodextrins could not be detected in low-dilution-rate,
cellulose-limited continuous cultures, but these cultures had a large
number of nonadherent cells. Because the nonadherent cells had a large
reserve of polysaccharide and were observed at all stages of cell division,
it appeared that they were utilizing cellodextrins as an energy source for
growth.(ABSTRACT TRUNCATED AT 250 WORDS)
Copyright © 1995, American Society for Microbiology
Cellodextrin efflux by the cellulolytic ruminal bacterium Fibrobacter succinogenes and its potential role in the growth of nonadherent bacteria
Section of Microbiology, Cornell University, Ithaca, New York 14853, USA.
This article has been cited by other articles:
| J. Bacteriol. | Microbiol. Mol. Biol. Rev. | Eukaryot. Cell | All ASM Journals |
|---|