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Nitrate reductase activity, nitrate uptake and iodine speciation in the marine environment.

机译:海洋环境中的硝酸还原酶活性,硝酸盐吸收和碘形态。

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摘要

The present method for the determination of new production (NP) by measuring the uptake of added 15NO3 suffers from a number of limitations. In an attempt to improve this situation, this research examined the possibility of estimating 15NO 3 uptake by measuring the activity of nitrate reductase (NRA). In addition, because it has long been suspected that the biological reduction of IO3 to I may be mediated by nitrate reductase (NR), this research investigated the ability of NR to catalyze the reduction of iodate to iodide.; An improved method for the determination of NRA was developed. The sensitivity of this method is about five times higher than methods used in previous studies. NRA and 15NO3 uptake (NU) were determined over a wide range of nitrate concentrations in the East China Sea and in the adjoining Kuroshio Current in May, 1996. In light and nitrate-replete waters ([NO3]>1 μM, %PAR > 10%, PAR: photosynthetically active radiance), NRA was linearly related to NP so that NRA may be used for estimating NP. A high ratio of NU/NRA was found in nitrate-depleted ([NO 3] 1 μM) and light-replete (%PAR > 10%) conditions. The high ratio of NU/NRA data might have been caused by an overestimation of NU due to the stimulation of the addition of 15NO3 to nitrate-deficient water. This result revealed that NRA may be a reliable index for estimating new production in oligotrophic waters. In comparing NU in the literature with our NU values in different hydrographic realms, the NU values estimated from NRA fall well with recently reported values in similar types of waters.; NRA and iodine speciation were measured in the East China Sea in May, 1996. The results suggest that the reduction of iodate to iodide in the upwelling areas is caused by the enzyme NR. In the process of iodate reduction, the depletion of iodate and the enrichment of iodide relative to the composition of the source water of a surface water mass represent an integration of NRA through the residence time of the water mass.; A method for estimating the reduction of iodate to iodide by NR by using 125IO3 was developed. The reduction of IO3 to I by NR was observed in the cultures of S. costatum and in natural phytoplankton assemblages. The rates were 0.008 to 0.019 n mol I μg chl a–1 h–1 in natural samples. The iodate reduction rate was linearly related to NRA, suggesting that iodate reduction may be coupled to nitrate reduction.
机译:通过测量添加的 15 NO 3 的摄取量来确定新产品(NP)的现有方法存在许多局限性。为了改善这种情况,本研究探讨了通过测量硝酸还原酶(NRA)的活性来估算 15 NO 3 摄取的可能性。 )。此外,由于长期以来一直怀疑IO 3 从生物还原到I 可能是由硝酸还原酶(NR)介导的,这项研究调查了NR催化将碘酸盐还原为碘化物的能力。开发了一种测定NRA的改进方法。这种方法的灵敏度大约是以前研究中使用的方法的五倍。在东海及毗邻黑潮的硝酸盐浓度范围内,测定了NRA和 15 NO 3 的摄取量当前于1996年5月。在淡水和富含硝酸盐的水中([NO 3 ]> 1μM,%PAR> 10%,PAR:光合有效辐射), NRA与NP线性相关,因此NRA可用于估算NP。在贫硝酸盐([NO 3 ] <1μM)和光照充足(%PAR> 10%)的条件下,发现NU / NRA的比例很高。 NU / NRA数据比率高可能是由于刺激了 15 NO 3 的刺激而导致的NU高估所致硝酸盐缺乏的水。该结果表明,NRA可能是估计贫营养水域新产量的可靠指标。在将文献中的NU值与我们在不同水文领域的NU值进行比较时,根据NRA估算的NU值与最近报告的类似类型水域中的NU值相吻合。 1996年5月在东海测量了NRA和碘的形态。结果表明,上升流区的碘酸盐还原为碘化物是由NR酶引起的。在碘酸盐还原过程中,相对于地表水团的源水组成而言,碘酸盐的消耗和碘化物的富集代表了NRA在水团停留时间中的积分。开发了一种利用 125 IO 3 估算NR将碘酸盐还原为碘化物的方法。在 S培养物中观察到NR将IO 3 还原为I 。 costatum 和天然浮游植物组合。天然样品中I μgchl a –1 h –1 的比率为0.008至0.019 n mol。碘酸盐的还原速率与NR​​A呈线性关系,表明碘酸盐的还原可能与硝酸盐的还原有关。

著录项

  • 作者

    Hung, Chin-Chang.;

  • 作者单位

    Old Dominion University.;

  • 授予单位 Old Dominion University.;
  • 学科 Biology Oceanography.; Chemistry Biochemistry.
  • 学位 Ph.D.
  • 年度 1999
  • 页码 200 p.
  • 总页数 200
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 海洋生物;生物化学;
  • 关键词

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