{"title":"从复合分子结构到多重超分子聚集体:分子间相互作用在生物表面活性剂自组装中的作用","authors":"Irene Russo Krauss , Rodolfo Esposito , Luigi Paduano , Gerardino D'Errico","doi":"10.1016/j.cocis.2024.101792","DOIUrl":null,"url":null,"abstract":"<div><p>Microbial biosurfactants are an attractive and promising class of molecules with the potential to replace oil-derived surfactants for the formulation of ecofriendly and biocompatible products. In this review, we discuss literature findings, mostly reported in the last decade, on the self-assembly of the four main classes of microbial biosurfactants, <em>i.e.</em>, rhamnolipids, mannosylerythritol lipids, sophorolipids, and surfactin. All of them present composite molecular structures, characterized by different functional groups and ionisable moieties, and a high conformational flexibility. Where possible, we discuss the formation of different aggregate morphologies in terms of biosurfactant molecular structure and variation of environmental parameters. We highlight how the biosurfactant self-assembly is regulated by a complex interplay between various intermolecular interactions, including H-bonds and steric constraints, besides electrostatic and hydrophobic interactions. For this reason, we show that common theoretical approaches to amphiphile self-assembly, such as the critical packing parameter, have limitations in rationalizing and predicting biosurfactant aggregation behaviour.</p></div>","PeriodicalId":293,"journal":{"name":"Current Opinion in Colloid & Interface Science","volume":null,"pages":null},"PeriodicalIF":7.9000,"publicationDate":"2024-02-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1359029424000104/pdfft?md5=ddb5edf77569fd45576a9e974856fa99&pid=1-s2.0-S1359029424000104-main.pdf","citationCount":"0","resultStr":"{\"title\":\"From composite molecular structures to a multiplicity of supramolecular aggregates: The role of intermolecular interactions in biosurfactant self-assembly\",\"authors\":\"Irene Russo Krauss , Rodolfo Esposito , Luigi Paduano , Gerardino D'Errico\",\"doi\":\"10.1016/j.cocis.2024.101792\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Microbial biosurfactants are an attractive and promising class of molecules with the potential to replace oil-derived surfactants for the formulation of ecofriendly and biocompatible products. In this review, we discuss literature findings, mostly reported in the last decade, on the self-assembly of the four main classes of microbial biosurfactants, <em>i.e.</em>, rhamnolipids, mannosylerythritol lipids, sophorolipids, and surfactin. All of them present composite molecular structures, characterized by different functional groups and ionisable moieties, and a high conformational flexibility. Where possible, we discuss the formation of different aggregate morphologies in terms of biosurfactant molecular structure and variation of environmental parameters. We highlight how the biosurfactant self-assembly is regulated by a complex interplay between various intermolecular interactions, including H-bonds and steric constraints, besides electrostatic and hydrophobic interactions. For this reason, we show that common theoretical approaches to amphiphile self-assembly, such as the critical packing parameter, have limitations in rationalizing and predicting biosurfactant aggregation behaviour.</p></div>\",\"PeriodicalId\":293,\"journal\":{\"name\":\"Current Opinion in Colloid & Interface Science\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":7.9000,\"publicationDate\":\"2024-02-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S1359029424000104/pdfft?md5=ddb5edf77569fd45576a9e974856fa99&pid=1-s2.0-S1359029424000104-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Current Opinion in Colloid & Interface Science\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1359029424000104\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Opinion in Colloid & Interface Science","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1359029424000104","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
摘要
微生物生物表面活性剂是一类极具吸引力和发展前景的分子,有可能取代源自石油的表面活性剂,用于配制生态友好和生物兼容的产品。在这篇综述中,我们将讨论有关四大类微生物生物表面活性剂(即鼠李糖醇脂类、甘露糖赤藓糖醇脂类、槐脂类和表面活性剂)自组装的文献发现,这些发现大多是在过去十年中报道的。所有这些生物表面活性剂都具有复合分子结构,其特点是具有不同的官能团和可电离分子,并且具有很高的构象灵活性。在可能的情况下,我们从生物表面活性剂分子结构和环境参数变化的角度讨论了不同聚合体形态的形成。我们强调了生物表面活性剂的自组装如何受到各种分子间相互作用的复杂影响,除了静电和疏水相互作用外,还包括 H 键和立体约束。因此,我们证明了双亲化合物自组装的常见理论方法(如临界堆积参数)在合理解释和预测生物表面活性剂的聚集行为方面存在局限性。
From composite molecular structures to a multiplicity of supramolecular aggregates: The role of intermolecular interactions in biosurfactant self-assembly
Microbial biosurfactants are an attractive and promising class of molecules with the potential to replace oil-derived surfactants for the formulation of ecofriendly and biocompatible products. In this review, we discuss literature findings, mostly reported in the last decade, on the self-assembly of the four main classes of microbial biosurfactants, i.e., rhamnolipids, mannosylerythritol lipids, sophorolipids, and surfactin. All of them present composite molecular structures, characterized by different functional groups and ionisable moieties, and a high conformational flexibility. Where possible, we discuss the formation of different aggregate morphologies in terms of biosurfactant molecular structure and variation of environmental parameters. We highlight how the biosurfactant self-assembly is regulated by a complex interplay between various intermolecular interactions, including H-bonds and steric constraints, besides electrostatic and hydrophobic interactions. For this reason, we show that common theoretical approaches to amphiphile self-assembly, such as the critical packing parameter, have limitations in rationalizing and predicting biosurfactant aggregation behaviour.
期刊介绍:
Current Opinion in Colloid and Interface Science (COCIS) is an international journal that focuses on the molecular and nanoscopic aspects of colloidal systems and interfaces in various scientific and technological fields. These include materials science, biologically-relevant systems, energy and environmental technologies, and industrial applications.
Unlike primary journals, COCIS primarily serves as a guide for researchers, helping them navigate through the vast landscape of recently published literature. It critically analyzes the state of the art, identifies bottlenecks and unsolved issues, and proposes future developments.
Moreover, COCIS emphasizes certain areas and papers that are considered particularly interesting and significant by the Editors and Section Editors. Its goal is to provide valuable insights and updates to the research community in these specialized areas.