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            <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/dataset/743018.rdf" xlink:actuate="onRequest">Microbial enzyme activities: peptidase activities of sediment samples from the RV\Polarstern cruise ARKXXVII/3 in the Central Arctic Ocean and Laptev Sea, Aug-Sept. 2012</gmx:Anchor>
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            <gco:CharacterString>Cite this dataset as: Arnosti, C. (2020) Microbial enzyme activities: peptidase activities of sediment samples from the RV\Polarstern cruise ARKXXVII/3 in the Central Arctic Ocean and Laptev Sea, Aug-Sept. 2012. Biological and Chemical Oceanography Data Management Office (BCO-DMO). (Version 1) Version Date 2018-07-24 [if applicable, indicate subset used]. doi:10.26008/1912/bco-dmo.743018.1 [access date]</gco:CharacterString>
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        <gco:CharacterString>ARK27-3: sediment MCA Dataset Description: &amp;lt;p&amp;gt;This dataset includes peptidase hydrolysis rates from sediments to measure microbial enzyme activities. Links to archived CTD data are also provided.&amp;amp;nbsp;Five substrates linked to a 7-amido-4-methyl coumarin (MCA) fluorophore, one amino acid – leucine – and four oligopeptides – the chymotrypsin substrates alanine-alanine-phenylalanine (AAF) and alanine-alanine-proline-phenylalanine (AAPF), and the trypsin substrates glutamine-alanine-arginine (QAR) and glutamic acid-gylcine-arginine (EGR) – were used to measure exo- and endo-acting peptidase activities, respectively.&amp;lt;/p&amp;gt; Methods and Sampling: &amp;lt;p&amp;gt;Surficial sediments were collected using a multi-corer.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Five substrates linked to a 7-amido-4-methyl coumarin (MCA) fluorophore, one amino acid – leucine – and four oligopeptides – the chymotrypsin substrates alanine-alanine-phenylalanine (AAF) and alanine-alanine-proline-phenylalanine (AAPF), and the trypsin substrates glutamine-alanine-arginine (QAR) and glutamic acid-gylcine-arginine (EGR) – were used to measure exo- and endo-acting peptidase activities, respectively. Hydrolysis rates of the substrates were measured as an increase in fluorescence as the fluorophore was hydrolyzed from the substrate over time [as in Hoppe, 1993; Obayashi and Suzuki, 2005]. For sediment measurements, peptidase activities were measured in a 1:2 (vol: vol) sediment: autoclaved seawater slurry. 100 micromolar concentrations of substrate were added to triplicate live and single autoclaved killed control incubations. 2 ml of slurry was centrifuged at each timepoint (0, 1h ,2h, and 4 h), filtered, and diluted with 1 ml borate buffer; fluorescence was measured in a 4 ml cuvette.&amp;amp;nbsp; Hydrolysis rates were calculated from the rate of increase of fluorescence in the incubation over time relative to a set of standards of known concentration of fluorophore.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;All incubations were conducted at 0 C in the dark.&amp;lt;/p&amp;gt;</gco:CharacterString>
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