Taiki Umezawa, Ira Novita Sari, Erina Yoshimura and Yasuyuki Nogata
{"title":"含有β-氨基酸†的新型沉降抑制寡肽","authors":"Taiki Umezawa, Ira Novita Sari, Erina Yoshimura and Yasuyuki Nogata","doi":"10.1039/D4SU00625A","DOIUrl":null,"url":null,"abstract":"<p >Efficient syntheses of tripeptides containing β-amino acids and their settlement inhibition activities toward two main foulants, the barnacle <em>Amphibalanus amphitrite</em> and the blue mussel <em>Mytilus galloprovincialis</em>, are described. The tripeptide design was inspired by a tripeptide fragment of dolastatin 16, a depsipeptide isolated from the sea hare <em>Dolabella auricularia</em>. Tripeptide with only α-amino acids did not exhibit settlement inhibition, while β-amino acid-containing tripeptides and dipeptides effectively prevented settlement. Made from inexpensive amino acids, these peptides are promising candidates for cost-effective and eco-friendly antifouling additives.</p>","PeriodicalId":74745,"journal":{"name":"RSC sustainability","volume":" 1","pages":" 540-545"},"PeriodicalIF":0.0000,"publicationDate":"2024-12-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2025/su/d4su00625a?page=search","citationCount":"0","resultStr":"{\"title\":\"Novel settlement inhibition oligopeptides containing β-amino acids†\",\"authors\":\"Taiki Umezawa, Ira Novita Sari, Erina Yoshimura and Yasuyuki Nogata\",\"doi\":\"10.1039/D4SU00625A\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Efficient syntheses of tripeptides containing β-amino acids and their settlement inhibition activities toward two main foulants, the barnacle <em>Amphibalanus amphitrite</em> and the blue mussel <em>Mytilus galloprovincialis</em>, are described. The tripeptide design was inspired by a tripeptide fragment of dolastatin 16, a depsipeptide isolated from the sea hare <em>Dolabella auricularia</em>. Tripeptide with only α-amino acids did not exhibit settlement inhibition, while β-amino acid-containing tripeptides and dipeptides effectively prevented settlement. Made from inexpensive amino acids, these peptides are promising candidates for cost-effective and eco-friendly antifouling additives.</p>\",\"PeriodicalId\":74745,\"journal\":{\"name\":\"RSC sustainability\",\"volume\":\" 1\",\"pages\":\" 540-545\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-12-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://pubs.rsc.org/en/content/articlepdf/2025/su/d4su00625a?page=search\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"RSC sustainability\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2025/su/d4su00625a\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"RSC sustainability","FirstCategoryId":"1085","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/su/d4su00625a","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Efficient syntheses of tripeptides containing β-amino acids and their settlement inhibition activities toward two main foulants, the barnacle Amphibalanus amphitrite and the blue mussel Mytilus galloprovincialis, are described. The tripeptide design was inspired by a tripeptide fragment of dolastatin 16, a depsipeptide isolated from the sea hare Dolabella auricularia. Tripeptide with only α-amino acids did not exhibit settlement inhibition, while β-amino acid-containing tripeptides and dipeptides effectively prevented settlement. Made from inexpensive amino acids, these peptides are promising candidates for cost-effective and eco-friendly antifouling additives.