{"id":{"repo_id":"uiuc","oai_identifier":"oai:www.ideals.illinois.edu:2142/20082"},"canonical_url":"https://search.dev.ndltd.org/etd/uiuc/oai:www.ideals.illinois.edu:2142/20082","repository":{"repo_id":"uiuc","name":"University of Illinois - Urbana-Champaign","base_url":"https://www.ideals.illinois.edu/oai-pmh"},"display":{"title":"The porphynoid pigments of the Caribbean tunicate Trididemnum solidum","abstract":"Tunichlorin, a nickel chlorin isolated from the Caribbean tunicate Trididemnum solidum, has been identified as nickel (II) 2-devinyl-2-hydroxymethylpyropheophorbide a by chemical and spectroscopic methods. A partial synthesis of dimethyl tunichlorin from chlorophyll a (7 steps, 5% overall yield) has also confirmed the proposed structure. In the living tunicate, tunichlorin appears to exist primarily as a series of C-14 to C-18 ester homologues (principally tunichlorin-COO-(C$\\sb3$H$\\sb4$O)-(CH$\\sb2$)$\\sb{14}$CH$\\sb3$). Preliminary studies suggest that tunichlorin esters are biosynthesized by the tunicate from alga-produced chlorophyll a. Although the biological function of tunichlorin esters remains unclear, analogy to related compounds suggests that they may be enzyme cofactors involved in reductive processes.","abstract_html":"Tunichlorin, a nickel chlorin isolated from the Caribbean tunicate Trididemnum solidum, has been identified as nickel (II) 2-devinyl-2-hydroxymethylpyropheophorbide a by chemical and spectroscopic methods. A partial synthesis of dimethyl tunichlorin from chlorophyll a (7 steps, 5% overall yield) has also confirmed the proposed structure. In the living tunicate, tunichlorin appears to exist primarily as a series of C-14 to C-18 ester homologues (principally tunichlorin-COO-(C$\\sb3$H$\\sb4$O)-(CH$\\sb2$)$\\sb{14}$CH$\\sb3$). Preliminary studies suggest that tunichlorin esters are biosynthesized by the tunicate from alga-produced chlorophyll a. Although the biological function of tunichlorin esters remains unclear, analogy to related compounds suggests that they may be enzyme cofactors involved in reductive processes.","abstract_has_math":true,"creators":["Bible, Keith Christopher"],"institution":"University of Illinois at Urbana-Champaign","degree_name":"Ph.D.","degree_level":"Dissertation","degree_discipline":"Chemistry","degree_department":null,"school":null,"contributors":["Rinehart, Kenneth L., Jr."],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2011,"date_issued":"2011-05-07T12:28:13Z","date_published":"2011-05-07T12:28:13Z","updated_at":"2026-07-22T22:25:15Z","subjects":["Chemistry, Biochemistry","Chemistry, Organic"],"languages":["eng"],"rights":["Copyright 1989 Bible, Keith Christopher"],"rights_urls":[],"identifier_entries":[{"key":"dc:identifier","label":"Identifier","values":["AAI9010806","(UMI)AAI9010806"],"render_values":[{"text":"AAI9010806","href":null,"code":true},{"text":"(UMI)AAI9010806","href":null,"code":true}]}]},"links":{"outbound_url":"http://hdl.handle.net/2142/20082","outbound_label":"Handle","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor","label":"Contributor","values":["Rinehart, Kenneth L., Jr."]},{"key":"dc:creator","label":"Author","values":["Bible, Keith Christopher"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date","label":"Dc Date","values":["2011-05-07T12:28:13Z","10000-01-01","1989"]},{"key":"dc:type","label":"Dc Type","values":["text"]},{"key":"thesis:degree_discipline","label":"Discipline","values":["Chemistry"]},{"key":"thesis:degree_level","label":"Degree Level","values":["Dissertation"]},{"key":"thesis:degree_name","label":"Degree Name","values":["Ph.D."]},{"key":"thesis:institution_name","label":"Thesis Institution Name","values":["University of Illinois at Urbana-Champaign"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["Chemistry, Biochemistry","Chemistry, Organic"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:language","label":"Dc Language","values":["eng"]},{"key":"dc:rights","label":"Dc Rights","values":["Copyright 1989 Bible, Keith Christopher"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier","label":"Identifier","values":["AAI9010806","(UMI)AAI9010806","http://hdl.handle.net/2142/20082"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description","label":"Description","values":["Tunichlorin, a nickel chlorin isolated from the Caribbean tunicate Trididemnum solidum, has been identified as nickel (II) 2-devinyl-2-hydroxymethylpyropheophorbide a by chemical and spectroscopic methods. A partial synthesis of dimethyl tunichlorin from chlorophyll a (7 steps, 5% overall yield) has also confirmed the proposed structure. In the living tunicate, tunichlorin appears to exist primarily as a series of C-14 to C-18 ester homologues (principally tunichlorin-COO-(C$\\sb3$H$\\sb4$O)-(CH$\\sb2$)$\\sb{14}$CH$\\sb3$). Preliminary studies suggest that tunichlorin esters are biosynthesized by the tunicate from alga-produced chlorophyll a. Although the biological function of tunichlorin esters remains unclear, analogy to related compounds suggests that they may be enzyme cofactors involved in reductive processes.","In addition to tunichlorin and tunichlorin esters, examination of T. solidum extracts also revealed the presence of several known porphynoids, including chlorophyll a, pheophytin a, 10-hydroxypheophytin a, pheophorbide a, 10-hydroxypheophorbide a, pyropheophytin a, and 10-hydroxychlorophyll a. In addition, isopropyl pheophorbide a was identified from extracts of isopropyl alcohol-preserved tunicate, suggestive of an artifact of work-up and highlighting the pitfalls of natural product isolations. A previously unreported chlorophyll a degradation product, purpurin-18 phytyl ester, was also found in tunicate extracts.","Made available in DSpace on 2011-05-07T12:28:13Z (GMT). No. of bitstreams: 2 license.txt: 4922 bytes, checksum: 910b249b4beec47e7ab768910c8f966f (MD5) 9010806.pdf: 4395127 bytes, checksum: 1feb3a26880a27d053ddb6f882c1aeca (MD5) Previous issue date: 1989","Item marked as restricted to the 'UIUC Users [automated]' Group (id=2) by Howard Ding (hding2@illinois.edu) on 2011-05-07T14:41:26Z Item is restricted indefinitely.","Restriction data tranferred 2014-07-01T11:17:55-05:00 Original Data Group with Access UIUC Users [automated] Release Date: none Reason: ETDs are only available to UIUC Users without author permission","ETDs are only available to UIUC Users without author permission","U of I Only"]},{"key":"dc:title","label":"Title","values":["The porphynoid pigments of the Caribbean tunicate Trididemnum solidum"]}]}],"canonical_facts":{"dc:contributor":["Rinehart, Kenneth L., Jr."],"dc:creator":["Bible, Keith Christopher"],"dc:date":["2011-05-07T12:28:13Z","10000-01-01","1989"],"dc:description":["Tunichlorin, a nickel chlorin isolated from the Caribbean tunicate Trididemnum solidum, has been identified as nickel (II) 2-devinyl-2-hydroxymethylpyropheophorbide a by chemical and spectroscopic methods. A partial synthesis of dimethyl tunichlorin from chlorophyll a (7 steps, 5% overall yield) has also confirmed the proposed structure. In the living tunicate, tunichlorin appears to exist primarily as a series of C-14 to C-18 ester homologues (principally tunichlorin-COO-(C$\\sb3$H$\\sb4$O)-(CH$\\sb2$)$\\sb{14}$CH$\\sb3$). Preliminary studies suggest that tunichlorin esters are biosynthesized by the tunicate from alga-produced chlorophyll a. Although the biological function of tunichlorin esters remains unclear, analogy to related compounds suggests that they may be enzyme cofactors involved in reductive processes.","In addition to tunichlorin and tunichlorin esters, examination of T. solidum extracts also revealed the presence of several known porphynoids, including chlorophyll a, pheophytin a, 10-hydroxypheophytin a, pheophorbide a, 10-hydroxypheophorbide a, pyropheophytin a, and 10-hydroxychlorophyll a. In addition, isopropyl pheophorbide a was identified from extracts of isopropyl alcohol-preserved tunicate, suggestive of an artifact of work-up and highlighting the pitfalls of natural product isolations. A previously unreported chlorophyll a degradation product, purpurin-18 phytyl ester, was also found in tunicate extracts.","Made available in DSpace on 2011-05-07T12:28:13Z (GMT). No. of bitstreams: 2 license.txt: 4922 bytes, checksum: 910b249b4beec47e7ab768910c8f966f (MD5) 9010806.pdf: 4395127 bytes, checksum: 1feb3a26880a27d053ddb6f882c1aeca (MD5) Previous issue date: 1989","Item marked as restricted to the 'UIUC Users [automated]' Group (id=2) by Howard Ding (hding2@illinois.edu) on 2011-05-07T14:41:26Z Item is restricted indefinitely.","Restriction data tranferred 2014-07-01T11:17:55-05:00 Original Data Group with Access UIUC Users [automated] Release Date: none Reason: ETDs are only available to UIUC Users without author permission","ETDs are only available to UIUC Users without author permission","U of I Only"],"dc:identifier":["AAI9010806","(UMI)AAI9010806","http://hdl.handle.net/2142/20082"],"dc:language":["eng"],"dc:rights":["Copyright 1989 Bible, Keith Christopher"],"dc:subject":["Chemistry, Biochemistry","Chemistry, Organic"],"dc:title":["The porphynoid pigments of the Caribbean tunicate Trididemnum solidum"],"dc:type":["text"],"thesis:degree_discipline":["Chemistry"],"thesis:degree_level":["Dissertation"],"thesis:degree_name":["Ph.D."],"thesis:institution_name":["University of Illinois at Urbana-Champaign"]},"updated_at":"2026-07-22T22:25:15Z"}