Construction of high-yielding edeine strains and an initial exploration of their control efficacy against crop pathogens

Abstract Background Edeine, a non-ribosomal antibiotic produced by Brevibacillus brevis X23, has a broad-spectrum antimicrobial activity against plant pathogens, but its low yield in wild-type strains limits its potential for agricultural applications. This study aimed to enhance edeine production b...

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Main Authors: Liang Zhang, Ziyue Chen, Fei Xia, Tianbo Liu, Qingshu Liu, Wu Chen
Format: Article
Language:English
Published: SpringerOpen 2025-05-01
Series:Chemical and Biological Technologies in Agriculture
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Online Access:https://doi.org/10.1186/s40538-025-00786-y
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author Liang Zhang
Ziyue Chen
Fei Xia
Tianbo Liu
Qingshu Liu
Wu Chen
author_facet Liang Zhang
Ziyue Chen
Fei Xia
Tianbo Liu
Qingshu Liu
Wu Chen
author_sort Liang Zhang
collection DOAJ
description Abstract Background Edeine, a non-ribosomal antibiotic produced by Brevibacillus brevis X23, has a broad-spectrum antimicrobial activity against plant pathogens, but its low yield in wild-type strains limits its potential for agricultural applications. This study aimed to enhance edeine production by genetically engineering B. brevis X23. Methods Red/ET homologous recombination technology was used to construct engineered strain X23(ΔabrB)::P mwp by knocking out global negative regulator AbrB and replacing the natural promoter of the edeine biosynthesis gene cluster (ede BGC) with the strong P mwp promoter. Results Quantitative PCR revealed significantly increased ede BGC transcription levels in X23(ΔabrB)::P mwp compared to the wild-type strain. High-performance liquid chromatography–mass spectrometry (HPLC–MS) demonstrated a 10.1-fold increase in the edeine peak area with the final yield reaching 97.3 mg/L. In pot experiments for tobacco bacterial wilt (pathogen name Ralstonia solanacearum) control, X23(ΔabrB)::P mwp showed an efficacy of 82.9%, representing a 32.6% improvement over the wild-type strain (62.5%). The engineered strain also demonstrated an increased plate inhibition capacity of 20.5–60.9% against Verticillium dahliae Kleb, Rhizoctonia solani, and Fusarium oxysporum in cotton, indicating its potential application in crop protection. Conclusions Therefore, this study yielded an engineered strain with increased edeine production and enhanced biocontrol efficacy, contributing to the development of biological control methods for plant diseases. Graphical Abstract
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spelling doaj-art-ddf067524a164b43881d82f5b8e1ca172025-08-20T01:52:22ZengSpringerOpenChemical and Biological Technologies in Agriculture2196-56412025-05-0112111710.1186/s40538-025-00786-yConstruction of high-yielding edeine strains and an initial exploration of their control efficacy against crop pathogensLiang Zhang0Ziyue Chen1Fei Xia2Tianbo Liu3Qingshu Liu4Wu Chen5College of Plant Protection, Hunan Agricultural UniversityCollege of Plant Protection, Hunan Agricultural UniversityCentral South University of Forestry and TechnologyHunan Tobacco Science Research InstituteInstitute of Microbiology, Hunan Academy of Agricultural Sciences, Yuelushan LaboratoryCollege of Plant Protection, Hunan Agricultural UniversityAbstract Background Edeine, a non-ribosomal antibiotic produced by Brevibacillus brevis X23, has a broad-spectrum antimicrobial activity against plant pathogens, but its low yield in wild-type strains limits its potential for agricultural applications. This study aimed to enhance edeine production by genetically engineering B. brevis X23. Methods Red/ET homologous recombination technology was used to construct engineered strain X23(ΔabrB)::P mwp by knocking out global negative regulator AbrB and replacing the natural promoter of the edeine biosynthesis gene cluster (ede BGC) with the strong P mwp promoter. Results Quantitative PCR revealed significantly increased ede BGC transcription levels in X23(ΔabrB)::P mwp compared to the wild-type strain. High-performance liquid chromatography–mass spectrometry (HPLC–MS) demonstrated a 10.1-fold increase in the edeine peak area with the final yield reaching 97.3 mg/L. In pot experiments for tobacco bacterial wilt (pathogen name Ralstonia solanacearum) control, X23(ΔabrB)::P mwp showed an efficacy of 82.9%, representing a 32.6% improvement over the wild-type strain (62.5%). The engineered strain also demonstrated an increased plate inhibition capacity of 20.5–60.9% against Verticillium dahliae Kleb, Rhizoctonia solani, and Fusarium oxysporum in cotton, indicating its potential application in crop protection. Conclusions Therefore, this study yielded an engineered strain with increased edeine production and enhanced biocontrol efficacy, contributing to the development of biological control methods for plant diseases. Graphical Abstracthttps://doi.org/10.1186/s40538-025-00786-yBrevibacillus brevisEdeineTranscriptional regulatorPromoterGenetic modificationBiocontrol
spellingShingle Liang Zhang
Ziyue Chen
Fei Xia
Tianbo Liu
Qingshu Liu
Wu Chen
Construction of high-yielding edeine strains and an initial exploration of their control efficacy against crop pathogens
Chemical and Biological Technologies in Agriculture
Brevibacillus brevis
Edeine
Transcriptional regulator
Promoter
Genetic modification
Biocontrol
title Construction of high-yielding edeine strains and an initial exploration of their control efficacy against crop pathogens
title_full Construction of high-yielding edeine strains and an initial exploration of their control efficacy against crop pathogens
title_fullStr Construction of high-yielding edeine strains and an initial exploration of their control efficacy against crop pathogens
title_full_unstemmed Construction of high-yielding edeine strains and an initial exploration of their control efficacy against crop pathogens
title_short Construction of high-yielding edeine strains and an initial exploration of their control efficacy against crop pathogens
title_sort construction of high yielding edeine strains and an initial exploration of their control efficacy against crop pathogens
topic Brevibacillus brevis
Edeine
Transcriptional regulator
Promoter
Genetic modification
Biocontrol
url https://doi.org/10.1186/s40538-025-00786-y
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