Skip to main content
Applied and Environmental Microbiology logoLink to Applied and Environmental Microbiology
. 1993 Jan;59(1):120–128. doi: 10.1128/aem.59.1.120-128.1993

Glucose Uptake and End Product Formation in an Intertidal Marine Sediment

T E Sawyer 1, G M King 1,*
PMCID: PMC202065  PMID: 16348837

Abstract

Glucose uptake was monitored on a seasonal basis, using [6-3H]glucose and undisturbed cores collected from an intertidal mud flat. The fate of glucose carbon, including the formation of CO2 and biomass, was assayed by using undisturbed cores and [U-14C]glucose; the production of short-chain fatty acids was monitored with [U-14C]glucose and sediment slurries. Rate constants for glucose uptake varied temporally, with temperature accounting for much of the variability; turnover times ranged from about 2 to 10 min. Rate constants decreased with increasing sediment depth and in the following order for several common monosaccharides: glucose>galactose>mannose∼fucose. Time course analyses of 14CO2 production provided evidence of significant isotopic dilution; although pore water glucose turnover times were on the order of minutes, 14CO2 did not plateau until after approximately 6 h of incubation. At this time a maximum of about 40% of the added radioglucose had been respired. The extent of respiration varied as a function of sediment depth and season, with the highest values below the surface (4 to 7 cm) and in summer and fall. Incorporation of radiolabelled glucose into biomass also varied seasonally, but the greatest extent of incorporation (about 40%) was observed in the fall and for the 0- to 1-cm depth interval. The production of short-chain fatty acid end products was largely limited to acetate, which accounted for only a small percentage of the added radiolabel. Other organic acids, pyruvate in particular, were observed in pore water and were due to artifacts in the heat-kill procedure used to terminate incubations. An accurate assessment of the distribution and importance of short-chain fatty acids as end products required the use of an enzymatic technique coupled with high-pressure liquid chromatography to verify qualitative identities.

Full text

PDF
120

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Canfield D. E. Sulfate reduction and oxic respiration in marine sediments: implications for organic carbon preservation in euxinic environments. Deep Sea Res A. 1989;36(1):121–138. doi: 10.1016/0198-0149(89)90022-8. [DOI] [PubMed] [Google Scholar]
  2. Harrison M. J., Wright R. T., Morita R. Y. Method for measuring mineralization in lake sediments. Appl Microbiol. 1971 Apr;21(4):698–702. doi: 10.1128/am.21.4.698-702.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. King G. M., Klug M. J. Glucose metabolism in sediments of a eutrophic lake: tracer analysis of uptake and product formation. Appl Environ Microbiol. 1982 Dec;44(6):1308–1317. doi: 10.1128/aem.44.6.1308-1317.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. King G. M., Klug M. J., Lovley D. R. Metabolism of acetate, methanol, and methylated amines in intertidal sediments of lowes cove, maine. Appl Environ Microbiol. 1983 Jun;45(6):1848–1853. doi: 10.1128/aem.45.6.1848-1853.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Lovley D. R., Klug M. J. Intermediary metabolism of organic matter in the sediments of a eutrophic lake. Appl Environ Microbiol. 1982 Mar;43(3):552–560. doi: 10.1128/aem.43.3.552-560.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Lovley D. R., Phillips E. J. Requirement for a Microbial Consortium To Completely Oxidize Glucose in Fe(III)-Reducing Sediments. Appl Environ Microbiol. 1989 Dec;55(12):3234–3236. doi: 10.1128/aem.55.12.3234-3236.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Sørensen J., Christensen D., Jørgensen B. B. Volatile Fatty acids and hydrogen as substrates for sulfate-reducing bacteria in anaerobic marine sediment. Appl Environ Microbiol. 1981 Jul;42(1):5–11. doi: 10.1128/aem.42.1.5-11.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Toerien D. F., Cavari B. Effect of temperature on heterotrophic glucose uptake, mineralization, and turnover rates in lake sediments. Appl Environ Microbiol. 1982 Jan;43(1):1–5. doi: 10.1128/aem.43.1.1-5.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Winfrey M. R., Ward D. M. Substrates for sulfate reduction and methane production in intertidal sediments. Appl Environ Microbiol. 1983 Jan;45(1):193–199. doi: 10.1128/aem.45.1.193-199.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Applied and Environmental Microbiology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES