2003
DOI: 10.3354/meps263001
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Ectohydrolase activity in surface waters of the Hudson River and western Long Island Sound estuaries

Abstract: Variability in hydrolytic ectoenzyme activity was investigated at 3 stations along the salinity gradient of the Hudson River estuary and at 1 station in western Long Island Sound between October 1996 and October 1998. Activities of aminopeptidase, β-glucosidase, chitinase, lipase and alkaline phosphatase were estimated at each station using fluorogenic substrate analogs (methylumbelliferyl [MUF]-and methylcoumarinylamide [MCA]-labeled). Potential hydrolysis rate constants for these ectohydrolases varied widely… Show more

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Cited by 48 publications
(35 citation statements)
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“…However, this author noticed also large day-to day fluctuations of ectoenzymatic activity and a prominent presence of lipase activity among isolates. Finally, nothing is known about the difference that can be obtained by using MUF-oleate (unsaturated fatty acid analog 18:1) and MUF-palmitate (saturated fatty acid analog 16:0 that we used) as fluorogenic substrates (Taylor et al, 2003).…”
Section: Bacterial Community Response To Nutrient Status Through Ectomentioning
confidence: 99%
“…However, this author noticed also large day-to day fluctuations of ectoenzymatic activity and a prominent presence of lipase activity among isolates. Finally, nothing is known about the difference that can be obtained by using MUF-oleate (unsaturated fatty acid analog 18:1) and MUF-palmitate (saturated fatty acid analog 16:0 that we used) as fluorogenic substrates (Taylor et al, 2003).…”
Section: Bacterial Community Response To Nutrient Status Through Ectomentioning
confidence: 99%
“…The Hudson River estuary experiences eutrophication from nutrient input in the New York/ New Jersey area (Taylor et al 2003). During the 8 April 2005 -20 April 2005 cruise aboard the RV Oceanus, EAAS sampled the ship's uncontaminated seawater system in the dry lab for peptidase using Leu-AMC as the substrate and a 5 min incubation.…”
Section: Gaas and Ammermanmentioning
confidence: 99%
“…High fluorescence yield and low background fluorescence will increase assay sensitivity (Ammerman and Glover 2000). Previous enzyme activity measurements have used incubation times ranging from a few hours to multiple days in oligotrophic regions (Perry 1972;Christian and Karl 1995;Taylor et al 2003;Kirchman et al 2004;Sebastian et al 2004). Although increasing incubation time does not affect the detection limit of fluorescence (there is no change in the quantum yield of the fluorescent compound), it does allow lower activities to be measured.…”
mentioning
confidence: 99%
“…At that rate, the mussels should have removed .80% of the entire free amino acid pool, excluding glutamate and aspartate, less than a day after each change of water (Baines et al 2005). Such a depletion is unlikely in situ, where zebra mussels typically filter a fraction of their ambient environment daily (Strayer 1999) and free amino acid pools are quickly turned over through the ectohydrolytic activity of microbes (Taylor et al 2003). If mussels in our experiments were in fact depleting these labile DOM pools, then the difference in growth rate between the high DOM and low DOM treatments should be greater when the water is replaced more frequently.…”
Section: Methodsmentioning
confidence: 99%