1975
DOI: 10.1073/pnas.72.6.2112
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Use of the adenylate energy charge ratio to measure growth state of natural microbial communities.

Abstract: Measurement of the adenylate energy charge ratio is proposed as a means of determining the growth state of natural microbial communities and the effect of environmental changes on them. Observations on microbial cultures and on natural microbial populations from the Western North Atlantic Ocean water and from sediments of a coastal salt marsh show that energy charge measurements do show the metabolic state of communities as well as species populations.

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Cited by 76 publications
(35 citation statements)
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“…First, it is nonspecific and is generally applicable: and second, its response to environmental changes is rapid, from minutes for microorganisms (Wiebe & Bancroft, 1975) to 24 h for a mollusc (Wijsman, 1976). Changes of the A EC have been observed in several studies with perturbations in environmental conditions (salinity, temperature, exposure to hydrocarbons, and lack of oxygen) or with growth state.…”
Section: Energy Statusmentioning
confidence: 99%
“…First, it is nonspecific and is generally applicable: and second, its response to environmental changes is rapid, from minutes for microorganisms (Wiebe & Bancroft, 1975) to 24 h for a mollusc (Wijsman, 1976). Changes of the A EC have been observed in several studies with perturbations in environmental conditions (salinity, temperature, exposure to hydrocarbons, and lack of oxygen) or with growth state.…”
Section: Energy Statusmentioning
confidence: 99%
“…In these microcosms, microbial biomass remained sufficiently high to support C. capitata activities. In addition, changes in DNA synthesis in microcosms with aerobic and anaerobic aged detritus followed the AEC ratio which is a relative measure of microbial growth rate (Wiebe and Bancroft, 1975). Therefore, if microbial biomass is high, C. capitata production is not tightly coupled to microbial production.…”
Section: Discussionmentioning
confidence: 99%
“…After grinding the frozen tissue with a mortar and pestle, the powder (about I mg of wet weight) was boiled immediately for 3 min in 1.5 ml of 50 mA/ Tris-HCI buffer, pH 7.75, containing 4 mM EDTA, to extract ATP [ 12], After adding 0.5 ml of ATP-releasing agent (An alytical Luminescence Laboratory, San Diego, Calif., USA), the extract was centrifuged at 2,500 rpm for 10 min, and cooled 4°C. The supernatant was used for the ATP assay, based on a linear bioluminescence response of luciferine-luciferase [ 13], using the Lumiphometer (TD4000, Labo Science, Tokyo, Japan).…”
Section: Methodsmentioning
confidence: 99%