Loading…
Photochemical and Nonphotochemical Transformations of Cysteine with Dissolved Organic Matter
Cysteine (Cys) plays numerous key roles in the biogeochemistry of natural waters. Despite its importance, a full assessment of Cys abiotic transformation kinetics, products and pathways under environmental conditions has not been conducted. This study is a mechanistic evaluation of the photochemical...
Saved in:
Published in: | Environmental science & technology 2016-06, Vol.50 (12), p.6363-6373 |
---|---|
Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-a394t-f07b699ce1480412f58e30888412956ef61ace67173b08e6f446c21a85e764773 |
---|---|
cites | cdi_FETCH-LOGICAL-a394t-f07b699ce1480412f58e30888412956ef61ace67173b08e6f446c21a85e764773 |
container_end_page | 6373 |
container_issue | 12 |
container_start_page | 6363 |
container_title | Environmental science & technology |
container_volume | 50 |
creator | Chu, Chiheng Erickson, Paul R Lundeen, Rachel A Stamatelatos, Dimitrios Alaimo, Peter J Latch, Douglas E McNeill, Kristopher |
description | Cysteine (Cys) plays numerous key roles in the biogeochemistry of natural waters. Despite its importance, a full assessment of Cys abiotic transformation kinetics, products and pathways under environmental conditions has not been conducted. This study is a mechanistic evaluation of the photochemical and nonphotochemical (dark) transformations of Cys in solutions containing chromophoric dissolved organic matter (CDOM). The results show that Cys underwent abiotic transformations under both dark and irradiated conditions. Under dark conditions, the transformation rates of Cys were moderate and were highly pH- and temperature-dependent. Under UVA or natural sunlight irradiations, Cys transformation rates were enhanced by up to two orders of magnitude compared to rates under dark conditions. Product analysis indicated cystine and cysteine sulfinic acid were the major photooxidation products. In addition, this study provides an assessment of the contributions of singlet oxygen, hydroxyl radical, hydrogen peroxide, and triplet dissolved organic matter to the CDOM-sensitized photochemical oxidation of Cys. The results suggest that another unknown pathway was dominant in the CDOM-sensitized photodegradation of Cys, which will require further study to identify. |
doi_str_mv | 10.1021/acs.est.6b01291 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1808739247</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>4099159401</sourcerecordid><originalsourceid>FETCH-LOGICAL-a394t-f07b699ce1480412f58e30888412956ef61ace67173b08e6f446c21a85e764773</originalsourceid><addsrcrecordid>eNqNkUtLAzEUhYMoWqtrdzLgRpCpN8lMHkupT_C1UHAhDGl6x47MTGoyVfz3prQqCoKrGy7fOTnJIWSHwoACo4fGhgGGbiBGQJmmK6RHcwZprnK6SnoAlKeai4cNshnCMwAwDmqdbDBJJeNS9cjj7cR1zk6wqaypE9OOk2vXTn8s77xpQ-l8Y7rKtSFxZTJ8Dx1WLSZvVTdJjqsQXP2K4-TGP5m2ssmV6Tr0W2StNHXA7eXsk_vTk7vheXp5c3YxPLpMDddZl5YgR0JrizRTkFFW5gpjTqXiWecCS0GNRREz8xEoFGWWCcuoUTlKkUnJ-2R_4Tv17mUW_6NoqmCxrk2LbhYKqkBJrln2D1RqpTXnIo_o3i_02c18Gx8ypzRjUgBE6nBBWe9C8FgWU181xr8XFIp5R0XsqJirlx1Fxe7SdzZqcPzFf5YSgYMFMFd-3_mH3QfH_5tp</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1799227600</pqid></control><display><type>article</type><title>Photochemical and Nonphotochemical Transformations of Cysteine with Dissolved Organic Matter</title><source>American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list)</source><creator>Chu, Chiheng ; Erickson, Paul R ; Lundeen, Rachel A ; Stamatelatos, Dimitrios ; Alaimo, Peter J ; Latch, Douglas E ; McNeill, Kristopher</creator><creatorcontrib>Chu, Chiheng ; Erickson, Paul R ; Lundeen, Rachel A ; Stamatelatos, Dimitrios ; Alaimo, Peter J ; Latch, Douglas E ; McNeill, Kristopher</creatorcontrib><description>Cysteine (Cys) plays numerous key roles in the biogeochemistry of natural waters. Despite its importance, a full assessment of Cys abiotic transformation kinetics, products and pathways under environmental conditions has not been conducted. This study is a mechanistic evaluation of the photochemical and nonphotochemical (dark) transformations of Cys in solutions containing chromophoric dissolved organic matter (CDOM). The results show that Cys underwent abiotic transformations under both dark and irradiated conditions. Under dark conditions, the transformation rates of Cys were moderate and were highly pH- and temperature-dependent. Under UVA or natural sunlight irradiations, Cys transformation rates were enhanced by up to two orders of magnitude compared to rates under dark conditions. Product analysis indicated cystine and cysteine sulfinic acid were the major photooxidation products. In addition, this study provides an assessment of the contributions of singlet oxygen, hydroxyl radical, hydrogen peroxide, and triplet dissolved organic matter to the CDOM-sensitized photochemical oxidation of Cys. The results suggest that another unknown pathway was dominant in the CDOM-sensitized photodegradation of Cys, which will require further study to identify.</description><identifier>ISSN: 0013-936X</identifier><identifier>EISSN: 1520-5851</identifier><identifier>DOI: 10.1021/acs.est.6b01291</identifier><identifier>PMID: 27172378</identifier><identifier>CODEN: ESTHAG</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Acidity ; Analytical chemistry ; Biogeochemistry ; Cysteine ; Dissolution ; Kinetics ; Photochemical Processes ; Photochemistry ; Photolysis ; Reaction kinetics ; Solutions ; Sunlight ; Temperature effects ; Ultraviolet radiation ; Water Pollutants, Chemical</subject><ispartof>Environmental science & technology, 2016-06, Vol.50 (12), p.6363-6373</ispartof><rights>Copyright © 2016 American Chemical Society</rights><rights>Copyright American Chemical Society Jun 21, 2016</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a394t-f07b699ce1480412f58e30888412956ef61ace67173b08e6f446c21a85e764773</citedby><cites>FETCH-LOGICAL-a394t-f07b699ce1480412f58e30888412956ef61ace67173b08e6f446c21a85e764773</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27898,27899</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27172378$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chu, Chiheng</creatorcontrib><creatorcontrib>Erickson, Paul R</creatorcontrib><creatorcontrib>Lundeen, Rachel A</creatorcontrib><creatorcontrib>Stamatelatos, Dimitrios</creatorcontrib><creatorcontrib>Alaimo, Peter J</creatorcontrib><creatorcontrib>Latch, Douglas E</creatorcontrib><creatorcontrib>McNeill, Kristopher</creatorcontrib><title>Photochemical and Nonphotochemical Transformations of Cysteine with Dissolved Organic Matter</title><title>Environmental science & technology</title><addtitle>Environ. Sci. Technol</addtitle><description>Cysteine (Cys) plays numerous key roles in the biogeochemistry of natural waters. Despite its importance, a full assessment of Cys abiotic transformation kinetics, products and pathways under environmental conditions has not been conducted. This study is a mechanistic evaluation of the photochemical and nonphotochemical (dark) transformations of Cys in solutions containing chromophoric dissolved organic matter (CDOM). The results show that Cys underwent abiotic transformations under both dark and irradiated conditions. Under dark conditions, the transformation rates of Cys were moderate and were highly pH- and temperature-dependent. Under UVA or natural sunlight irradiations, Cys transformation rates were enhanced by up to two orders of magnitude compared to rates under dark conditions. Product analysis indicated cystine and cysteine sulfinic acid were the major photooxidation products. In addition, this study provides an assessment of the contributions of singlet oxygen, hydroxyl radical, hydrogen peroxide, and triplet dissolved organic matter to the CDOM-sensitized photochemical oxidation of Cys. The results suggest that another unknown pathway was dominant in the CDOM-sensitized photodegradation of Cys, which will require further study to identify.</description><subject>Acidity</subject><subject>Analytical chemistry</subject><subject>Biogeochemistry</subject><subject>Cysteine</subject><subject>Dissolution</subject><subject>Kinetics</subject><subject>Photochemical Processes</subject><subject>Photochemistry</subject><subject>Photolysis</subject><subject>Reaction kinetics</subject><subject>Solutions</subject><subject>Sunlight</subject><subject>Temperature effects</subject><subject>Ultraviolet radiation</subject><subject>Water Pollutants, Chemical</subject><issn>0013-936X</issn><issn>1520-5851</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqNkUtLAzEUhYMoWqtrdzLgRpCpN8lMHkupT_C1UHAhDGl6x47MTGoyVfz3prQqCoKrGy7fOTnJIWSHwoACo4fGhgGGbiBGQJmmK6RHcwZprnK6SnoAlKeai4cNshnCMwAwDmqdbDBJJeNS9cjj7cR1zk6wqaypE9OOk2vXTn8s77xpQ-l8Y7rKtSFxZTJ8Dx1WLSZvVTdJjqsQXP2K4-TGP5m2ssmV6Tr0W2StNHXA7eXsk_vTk7vheXp5c3YxPLpMDddZl5YgR0JrizRTkFFW5gpjTqXiWecCS0GNRREz8xEoFGWWCcuoUTlKkUnJ-2R_4Tv17mUW_6NoqmCxrk2LbhYKqkBJrln2D1RqpTXnIo_o3i_02c18Gx8ypzRjUgBE6nBBWe9C8FgWU181xr8XFIp5R0XsqJirlx1Fxe7SdzZqcPzFf5YSgYMFMFd-3_mH3QfH_5tp</recordid><startdate>20160621</startdate><enddate>20160621</enddate><creator>Chu, Chiheng</creator><creator>Erickson, Paul R</creator><creator>Lundeen, Rachel A</creator><creator>Stamatelatos, Dimitrios</creator><creator>Alaimo, Peter J</creator><creator>Latch, Douglas E</creator><creator>McNeill, Kristopher</creator><general>American Chemical Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7ST</scope><scope>7T7</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>SOI</scope><scope>7X8</scope></search><sort><creationdate>20160621</creationdate><title>Photochemical and Nonphotochemical Transformations of Cysteine with Dissolved Organic Matter</title><author>Chu, Chiheng ; Erickson, Paul R ; Lundeen, Rachel A ; Stamatelatos, Dimitrios ; Alaimo, Peter J ; Latch, Douglas E ; McNeill, Kristopher</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a394t-f07b699ce1480412f58e30888412956ef61ace67173b08e6f446c21a85e764773</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Acidity</topic><topic>Analytical chemistry</topic><topic>Biogeochemistry</topic><topic>Cysteine</topic><topic>Dissolution</topic><topic>Kinetics</topic><topic>Photochemical Processes</topic><topic>Photochemistry</topic><topic>Photolysis</topic><topic>Reaction kinetics</topic><topic>Solutions</topic><topic>Sunlight</topic><topic>Temperature effects</topic><topic>Ultraviolet radiation</topic><topic>Water Pollutants, Chemical</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chu, Chiheng</creatorcontrib><creatorcontrib>Erickson, Paul R</creatorcontrib><creatorcontrib>Lundeen, Rachel A</creatorcontrib><creatorcontrib>Stamatelatos, Dimitrios</creatorcontrib><creatorcontrib>Alaimo, Peter J</creatorcontrib><creatorcontrib>Latch, Douglas E</creatorcontrib><creatorcontrib>McNeill, Kristopher</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Environment Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Environmental science & technology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chu, Chiheng</au><au>Erickson, Paul R</au><au>Lundeen, Rachel A</au><au>Stamatelatos, Dimitrios</au><au>Alaimo, Peter J</au><au>Latch, Douglas E</au><au>McNeill, Kristopher</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Photochemical and Nonphotochemical Transformations of Cysteine with Dissolved Organic Matter</atitle><jtitle>Environmental science & technology</jtitle><addtitle>Environ. Sci. Technol</addtitle><date>2016-06-21</date><risdate>2016</risdate><volume>50</volume><issue>12</issue><spage>6363</spage><epage>6373</epage><pages>6363-6373</pages><issn>0013-936X</issn><eissn>1520-5851</eissn><coden>ESTHAG</coden><abstract>Cysteine (Cys) plays numerous key roles in the biogeochemistry of natural waters. Despite its importance, a full assessment of Cys abiotic transformation kinetics, products and pathways under environmental conditions has not been conducted. This study is a mechanistic evaluation of the photochemical and nonphotochemical (dark) transformations of Cys in solutions containing chromophoric dissolved organic matter (CDOM). The results show that Cys underwent abiotic transformations under both dark and irradiated conditions. Under dark conditions, the transformation rates of Cys were moderate and were highly pH- and temperature-dependent. Under UVA or natural sunlight irradiations, Cys transformation rates were enhanced by up to two orders of magnitude compared to rates under dark conditions. Product analysis indicated cystine and cysteine sulfinic acid were the major photooxidation products. In addition, this study provides an assessment of the contributions of singlet oxygen, hydroxyl radical, hydrogen peroxide, and triplet dissolved organic matter to the CDOM-sensitized photochemical oxidation of Cys. The results suggest that another unknown pathway was dominant in the CDOM-sensitized photodegradation of Cys, which will require further study to identify.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>27172378</pmid><doi>10.1021/acs.est.6b01291</doi><tpages>11</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0013-936X |
ispartof | Environmental science & technology, 2016-06, Vol.50 (12), p.6363-6373 |
issn | 0013-936X 1520-5851 |
language | eng |
recordid | cdi_proquest_miscellaneous_1808739247 |
source | American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list) |
subjects | Acidity Analytical chemistry Biogeochemistry Cysteine Dissolution Kinetics Photochemical Processes Photochemistry Photolysis Reaction kinetics Solutions Sunlight Temperature effects Ultraviolet radiation Water Pollutants, Chemical |
title | Photochemical and Nonphotochemical Transformations of Cysteine with Dissolved Organic Matter |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-27T10%3A28%3A00IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Photochemical%20and%20Nonphotochemical%20Transformations%20of%20Cysteine%20with%20Dissolved%20Organic%20Matter&rft.jtitle=Environmental%20science%20&%20technology&rft.au=Chu,%20Chiheng&rft.date=2016-06-21&rft.volume=50&rft.issue=12&rft.spage=6363&rft.epage=6373&rft.pages=6363-6373&rft.issn=0013-936X&rft.eissn=1520-5851&rft.coden=ESTHAG&rft_id=info:doi/10.1021/acs.est.6b01291&rft_dat=%3Cproquest_cross%3E4099159401%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-a394t-f07b699ce1480412f58e30888412956ef61ace67173b08e6f446c21a85e764773%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1799227600&rft_id=info:pmid/27172378&rfr_iscdi=true |