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Applied and Environmental Microbiology, October 1998, p. 3838-3845, Vol. 64, No. 10
Istituto Scienze Ambientali Marine,
Received 26 March 1998/Accepted 23 July 1998
Enzymatic activities of aminopeptidase and
0099-2240/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Enzymatic Activity, Bacterial Distribution, and
Organic Matter Composition in Sediments of the Ross Sea
(Antarctica)
-glucosidase were
investigated in Antarctic Ross Sea sediments at two sites (sites B and
C, 567 and 439 m deep, respectively). The sites differed in
trophic conditions related to organic matter (OM) composition and
bacterial distribution. Carbohydrate concentrations at site B were
about double those at site C, while protein and lipid levels were 10 times higher. Proteins were mainly found in a soluble fraction
(>90%). Chloropigment content was generally low and phaeopigments were almost absent, indicating the presence of reduced inputs of
primary organic matter. ATP concentrations (as a measure of the living
microbial biomass) were significantly higher at site B. By contrast,
benthic bacterial densities at site C were about double those at site
B. Bacterial parameters do not appear to be "bottom-up controlled"
by the amount of available food but rather "top-down controlled" by
meiofauna predatory pressure, which was significantly higher at site B. Aminopeptidase and
-glucosidase extracellular enzyme activities
(EEA) in Antarctic sediments appear to be high and comparable to those
reported for temperate or Arctic sediments and characterized by low
aminopeptidase/
-glucosidase ratios (about 10). Activity profiles
showed decreasing patterns with increasing sediment depth, indicating
vertical shifts in both availability and nutritional quality of
degradable OM. Vertical profiles of aminopeptidase activity were
related to a decrease in protein concentration and/or to an increase in
the insoluble refractory proteinaceous fraction. The highest
aminopeptidase activity rates were observed at site C, characterized by
much lower protein concentrations. Differences in EEA between sites do
not seem to be explained by differences in the in situ temperature (
1.6 and
0.8°C at sites B and C, respectively). Aminopeptidase activity profiles are consistent with the bacterial biomass and frequency of dividing cells. Enzyme substrate affinity was generally dependent upon substrate concentrations. EEA, normalized to bacterial numbers, indicated specific activities comparable to those reported for
equally deep sediments at temperate latitudes. Vertical patterns of
specific enzymatic activity appeared to be controlled by chloroplastic pigment concentrations that accumulate in the deeper sediment layers.
The overall conclusion from the analysis of EEA in Antarctic sediments
is that enzyme-dependent transformations of OM proceed at rates similar
to those measured in temperate environments. Protein carbon potentially
liberated by aminopeptidase activities (12.597 to 26.190 mg of C
m
2 day
1) indicates that the whole protein
pool could be mobilized within 1.3 to 17 h. Carbohydrate carbon
mobilization (773 to 2,552 mg of C m
2 day
1)
is sufficient to turn over the carbohydrate pool within 16 to 20 h. Such rates are 6 to 45 times higher than fluxes of particulate organic proteins and carbohydrates, indicating an "uncoupled
hydrolysis" by the Antarctic benthic assemblages, in which bacteria
appear to be able to rapidly exploit episodic OM pulses.
*
Corresponding author. Mailing address: Marine Biology
Section, Faculty of Science, University of Ancona, Via Brecce Bianche, Monte D'Ago, 60131 Ancona, Italy. Phone: 39 71 220 4654. Fax: 39 71 220 4650. E-mail: danovaro{at}popcsi.unian.it.
Applied and Environmental Microbiology, October 1998, p. 3838-3845, Vol. 64, No. 10
0099-2240/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
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