用微孔板阅读器光度法测定海水介质中铵和磷酸盐

IF 1.2 Q2 Biochemistry, Genetics and Molecular Biology
Hanna S. Ruppersberg, M. R. Goebel, S. I. Kleinert, Daniel Wünsch, K. Trautwein, R. Rabus
{"title":"用微孔板阅读器光度法测定海水介质中铵和磷酸盐","authors":"Hanna S. Ruppersberg, M. R. Goebel, S. I. Kleinert, Daniel Wünsch, K. Trautwein, R. Rabus","doi":"10.1159/000454814","DOIUrl":null,"url":null,"abstract":"To more efficiently process the large sample numbers for quantitative determination of ammonium (NH<sub>4</sub><sup>+</sup>) and phosphate (orthophosphate, PO<sub>4</sub><sup>3-</sup>) generated during comprehensive growth experiments with the marine Roseobacter group member Phaeobacter inhibens DSM 17395, specific colorimetric assays employing a microplate reader (MPR) were established. The NH<sub>4</sub><sup>+</sup> assay is based on the reaction of NH<sub>4</sub><sup>+</sup> with hypochlorite and salicylate, yielding a limit of detection of 14 µ<smlcap>M</smlcap>, a limit of quantitation of 36 µ<smlcap>M,</smlcap> and a linear range for quantitative determination up to 200 µ<smlcap>M</smlcap>. The PO<sub>4</sub><sup>3-</sup>assay is based on the complex formation of PO<sub>4</sub><sup>3-</sup> with ammonium molybdate in the presence of ascorbate and zinc acetate, yielding a limit of detection of 13 µ<smlcap>M</smlcap>, a limit of quantitation of 50 µ<smlcap>M,</smlcap> and a linear range for quantitative determination up to 1 m<smlcap>M</smlcap>. Both MPR-based assays allowed for fast (significantly lower than 1 h) analysis of 21 samples plus standards for calibration (all measured in triplicates) and showed only low variation across a large collection of biological samples.","PeriodicalId":16370,"journal":{"name":"Journal of Molecular Microbiology and Biotechnology","volume":null,"pages":null},"PeriodicalIF":1.2000,"publicationDate":"2017-02-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000454814","citationCount":"10","resultStr":"{\"title\":\"Photometric Determination of Ammonium and Phosphate in Seawater Medium Using a Microplate Reader\",\"authors\":\"Hanna S. Ruppersberg, M. R. Goebel, S. I. Kleinert, Daniel Wünsch, K. Trautwein, R. Rabus\",\"doi\":\"10.1159/000454814\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"To more efficiently process the large sample numbers for quantitative determination of ammonium (NH<sub>4</sub><sup>+</sup>) and phosphate (orthophosphate, PO<sub>4</sub><sup>3-</sup>) generated during comprehensive growth experiments with the marine Roseobacter group member Phaeobacter inhibens DSM 17395, specific colorimetric assays employing a microplate reader (MPR) were established. The NH<sub>4</sub><sup>+</sup> assay is based on the reaction of NH<sub>4</sub><sup>+</sup> with hypochlorite and salicylate, yielding a limit of detection of 14 µ<smlcap>M</smlcap>, a limit of quantitation of 36 µ<smlcap>M,</smlcap> and a linear range for quantitative determination up to 200 µ<smlcap>M</smlcap>. The PO<sub>4</sub><sup>3-</sup>assay is based on the complex formation of PO<sub>4</sub><sup>3-</sup> with ammonium molybdate in the presence of ascorbate and zinc acetate, yielding a limit of detection of 13 µ<smlcap>M</smlcap>, a limit of quantitation of 50 µ<smlcap>M,</smlcap> and a linear range for quantitative determination up to 1 m<smlcap>M</smlcap>. Both MPR-based assays allowed for fast (significantly lower than 1 h) analysis of 21 samples plus standards for calibration (all measured in triplicates) and showed only low variation across a large collection of biological samples.\",\"PeriodicalId\":16370,\"journal\":{\"name\":\"Journal of Molecular Microbiology and Biotechnology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":1.2000,\"publicationDate\":\"2017-02-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1159/000454814\",\"citationCount\":\"10\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Molecular Microbiology and Biotechnology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1159/000454814\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"Biochemistry, Genetics and Molecular Biology\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Molecular Microbiology and Biotechnology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1159/000454814","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 10

摘要

为了更有效地处理大量样品,定量测定海洋玫瑰杆菌群成员Phaeobacter inhibens DSM 17395综合生长实验中产生的铵(NH4+)和磷酸盐(正磷酸盐,PO43-),采用微孔板检测仪(MPR)建立了特异性比色法。NH4+测定是基于NH4+与次氯酸盐和水杨酸盐的反应,产生14µM的检测限,36µM的定量限,定量测定的线性范围可达200µM。PO43-assay是基于复杂的形成与钼酸铵PO43 -抗坏血酸盐和醋酸锌,屈服极限的检测13µM,定量的限制50µM和定量测定的线性范围1毫米。两个MPR-based化验可以快速(明显低于1 h)分析21 +标准校准样品(所有以一式三份),只显示低跨大量生物样本变异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Photometric Determination of Ammonium and Phosphate in Seawater Medium Using a Microplate Reader
To more efficiently process the large sample numbers for quantitative determination of ammonium (NH4+) and phosphate (orthophosphate, PO43-) generated during comprehensive growth experiments with the marine Roseobacter group member Phaeobacter inhibens DSM 17395, specific colorimetric assays employing a microplate reader (MPR) were established. The NH4+ assay is based on the reaction of NH4+ with hypochlorite and salicylate, yielding a limit of detection of 14 µM, a limit of quantitation of 36 µM, and a linear range for quantitative determination up to 200 µM. The PO43-assay is based on the complex formation of PO43- with ammonium molybdate in the presence of ascorbate and zinc acetate, yielding a limit of detection of 13 µM, a limit of quantitation of 50 µM, and a linear range for quantitative determination up to 1 mM. Both MPR-based assays allowed for fast (significantly lower than 1 h) analysis of 21 samples plus standards for calibration (all measured in triplicates) and showed only low variation across a large collection of biological samples.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Journal of Molecular Microbiology and Biotechnology
Journal of Molecular Microbiology and Biotechnology 生物-生物工程与应用微生物
CiteScore
3.90
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: We are entering a new and exciting era of microbiological study and application. Recent advances in the now established disciplines of genomics, proteomics and bioinformatics, together with extensive cooperation between academic and industrial concerns have brought about an integration of basic and applied microbiology as never before.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信