{"title":"Biogenesis, structural diversity, biosynthesis and bioactivities of linear peptides from cyanobacteria.","authors":"Xinhai Li, Bo Zhang, Xiaoting Qiu","doi":"10.1016/j.bioorg.2026.110228","DOIUrl":null,"url":null,"abstract":"<p><p>Cyanobacteria are ancient photosynthetic Gram-negative prokaryotes widely distributed in various aquatic environments, exhibiting strong adaptability and the capacity to produce a diverse range of secondary metabolites. Among these metabolites, different types of peptides, including linear and cyclic peptides, are the dominant compounds. Although a number of in-depth studies on various linear peptides originating from cyanobacteria have been published, there has not yet been a comprehensive review that systematically summarizes the diverse research on these linear peptides. This article provides a systematic overview of the research progress on 19 classes of well-studied cyanobacteria-derived linear peptides, including short chain linear peptides, fatty acid modified linear peptides, linear peptides containing specialized cyclic moieties and long chain linear peptides, focusing on their biogenesis, structural diversity, biosynthesis as well as bioactivities. These linear peptides have emerged as promising candidates for developing anticancer, anticoagulant, anti-inflammatory and antiparasitic agents due to their versatile bioactivities and structural modifiability. Integrated chemical and biosynthetic strategies offer novel approaches to enhance production efficiency and optimize the pharmacological properties of these peptides. Future research will focus on overcoming the stability limitations of these linear peptides and expanding their therapeutic applications, aiming to unlock their full potential in addressing unmet medical challenges.</p>","PeriodicalId":257,"journal":{"name":"Bioorganic Chemistry","volume":"180 ","pages":"110228"},"PeriodicalIF":5.1000,"publicationDate":"2026-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bioorganic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1016/j.bioorg.2026.110228","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/7/7 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Cyanobacteria are ancient photosynthetic Gram-negative prokaryotes widely distributed in various aquatic environments, exhibiting strong adaptability and the capacity to produce a diverse range of secondary metabolites. Among these metabolites, different types of peptides, including linear and cyclic peptides, are the dominant compounds. Although a number of in-depth studies on various linear peptides originating from cyanobacteria have been published, there has not yet been a comprehensive review that systematically summarizes the diverse research on these linear peptides. This article provides a systematic overview of the research progress on 19 classes of well-studied cyanobacteria-derived linear peptides, including short chain linear peptides, fatty acid modified linear peptides, linear peptides containing specialized cyclic moieties and long chain linear peptides, focusing on their biogenesis, structural diversity, biosynthesis as well as bioactivities. These linear peptides have emerged as promising candidates for developing anticancer, anticoagulant, anti-inflammatory and antiparasitic agents due to their versatile bioactivities and structural modifiability. Integrated chemical and biosynthetic strategies offer novel approaches to enhance production efficiency and optimize the pharmacological properties of these peptides. Future research will focus on overcoming the stability limitations of these linear peptides and expanding their therapeutic applications, aiming to unlock their full potential in addressing unmet medical challenges.
期刊介绍:
Bioorganic Chemistry publishes research that addresses biological questions at the molecular level, using organic chemistry and principles of physical organic chemistry. The scope of the journal covers a range of topics at the organic chemistry-biology interface, including: enzyme catalysis, biotransformation and enzyme inhibition; nucleic acids chemistry; medicinal chemistry; natural product chemistry, natural product synthesis and natural product biosynthesis; antimicrobial agents; lipid and peptide chemistry; biophysical chemistry; biological probes; bio-orthogonal chemistry and biomimetic chemistry.
For manuscripts dealing with synthetic bioactive compounds, the Journal requires that the molecular target of the compounds described must be known, and must be demonstrated experimentally in the manuscript. For studies involving natural products, if the molecular target is unknown, some data beyond simple cell-based toxicity studies to provide insight into the mechanism of action is required. Studies supported by molecular docking are welcome, but must be supported by experimental data. The Journal does not consider manuscripts that are purely theoretical or computational in nature.
The Journal publishes regular articles, short communications and reviews. Reviews are normally invited by Editors or Editorial Board members. Authors of unsolicited reviews should first contact an Editor or Editorial Board member to determine whether the proposed article is within the scope of the Journal.