Optimization of fermentation conditions to increase the production of antifungal metabolites from Streptomyces sp. KN37

Abstract The bacterium Streptomyces sp. KN37 was isolated from the soil of Kanas, Xinjiang. The broth dilution of strain KN37 has a strong inhibitory effect against a variety of crop pathogenic fungi. However, in practical applications, its effective biological activity is limited by medium formulat...

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Main Authors: Xiaoyue Yang, Lijing Yuan, Muhammad Zeeshan, Chuntian Yang, Wen Gao, Guoqiang Zhang, Chunjuan Wang
Format: Article
Language:English
Published: BMC 2025-01-01
Series:Microbial Cell Factories
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Online Access:https://doi.org/10.1186/s12934-025-02652-w
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author Xiaoyue Yang
Lijing Yuan
Muhammad Zeeshan
Chuntian Yang
Wen Gao
Guoqiang Zhang
Chunjuan Wang
author_facet Xiaoyue Yang
Lijing Yuan
Muhammad Zeeshan
Chuntian Yang
Wen Gao
Guoqiang Zhang
Chunjuan Wang
author_sort Xiaoyue Yang
collection DOAJ
description Abstract The bacterium Streptomyces sp. KN37 was isolated from the soil of Kanas, Xinjiang. The broth dilution of strain KN37 has a strong inhibitory effect against a variety of crop pathogenic fungi. However, in practical applications, its effective biological activity is limited by medium formulations and fermentation conditions. In this study, we used the response surface method to optimize the fermentation medium and conditions of the strain KN37, for investigating the reasons for the enhanced biological activity at both the metabolic and transcriptomic levels. The results of the Plackett-Burman design showed that millet, yeast extract, and K2HPO4 were the key factors influencing its antifungal activity. Subsequently, optimization by the response surface methodology yielded the final fermentation conditions as: millet 20 g/L, yeast extract 1 g/L, K2HPO4 0.5 g/L, rotation speed 150 r/min, temperature 25 °C, initial pH 8, fermentation time 9 d, inoculation amount 4%, liquid volume 100 mL. The antifungal effect of the optimized strain fermentation dilution was significantly enhanced, and the antifungal rate of R. solani increased from 27.33 to 59.53%, closely aligning with the predicted value of 53.03%. The results of HPLC-MS/MS and transcriptomic analysis revealed that the content of some secondary metabolic active substances in the fermentation broth of KN37 was significantly different from that of the original fermentation broth. Notably, the content of 4- (diethylamino) salicylaldehyde (DSA) was significantly increased by 16.28-fold while the yield of N- (2,4-dimethylphenyl) formamide (NDMPF) was increased by 6.35 times. Transcriptomic analysis further elucidated molecular mechanisms behind these changes with the expression of salicylic acid dehydrogenase (SALD) was significantly down-regulated, which was only 0.48 times compared to that before optimization. This research successfully optimized the fermentation process of strain KN37 providing a strong foundation for the actual production and application of strain KN37 in agriculture.
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institution Kabale University
issn 1475-2859
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spelling doaj-art-ea97a5f2f33446b09fcb200950183e252025-01-26T12:58:51ZengBMCMicrobial Cell Factories1475-28592025-01-0124111310.1186/s12934-025-02652-wOptimization of fermentation conditions to increase the production of antifungal metabolites from Streptomyces sp. KN37Xiaoyue Yang0Lijing Yuan1Muhammad Zeeshan2Chuntian Yang3Wen Gao4Guoqiang Zhang5Chunjuan Wang6The Key Laboratory of Oasis Agricultural Pest Management and Plant Protection Utilization, College of Agriculture, Shihezi UniversityThe Key Laboratory of Oasis Agricultural Pest Management and Plant Protection Utilization, College of Agriculture, Shihezi UniversityThe Key Laboratory of Oasis Agricultural Pest Management and Plant Protection Utilization, College of Agriculture, Shihezi UniversityThe Key Laboratory of Oasis Agricultural Pest Management and Plant Protection Utilization, College of Agriculture, Shihezi UniversityThe Key Laboratory of Oasis Agricultural Pest Management and Plant Protection Utilization, College of Agriculture, Shihezi UniversityThe Key Laboratory of Oasis Agricultural Pest Management and Plant Protection Utilization, College of Agriculture, Shihezi UniversityThe Key Laboratory of Oasis Agricultural Pest Management and Plant Protection Utilization, College of Agriculture, Shihezi UniversityAbstract The bacterium Streptomyces sp. KN37 was isolated from the soil of Kanas, Xinjiang. The broth dilution of strain KN37 has a strong inhibitory effect against a variety of crop pathogenic fungi. However, in practical applications, its effective biological activity is limited by medium formulations and fermentation conditions. In this study, we used the response surface method to optimize the fermentation medium and conditions of the strain KN37, for investigating the reasons for the enhanced biological activity at both the metabolic and transcriptomic levels. The results of the Plackett-Burman design showed that millet, yeast extract, and K2HPO4 were the key factors influencing its antifungal activity. Subsequently, optimization by the response surface methodology yielded the final fermentation conditions as: millet 20 g/L, yeast extract 1 g/L, K2HPO4 0.5 g/L, rotation speed 150 r/min, temperature 25 °C, initial pH 8, fermentation time 9 d, inoculation amount 4%, liquid volume 100 mL. The antifungal effect of the optimized strain fermentation dilution was significantly enhanced, and the antifungal rate of R. solani increased from 27.33 to 59.53%, closely aligning with the predicted value of 53.03%. The results of HPLC-MS/MS and transcriptomic analysis revealed that the content of some secondary metabolic active substances in the fermentation broth of KN37 was significantly different from that of the original fermentation broth. Notably, the content of 4- (diethylamino) salicylaldehyde (DSA) was significantly increased by 16.28-fold while the yield of N- (2,4-dimethylphenyl) formamide (NDMPF) was increased by 6.35 times. Transcriptomic analysis further elucidated molecular mechanisms behind these changes with the expression of salicylic acid dehydrogenase (SALD) was significantly down-regulated, which was only 0.48 times compared to that before optimization. This research successfully optimized the fermentation process of strain KN37 providing a strong foundation for the actual production and application of strain KN37 in agriculture.https://doi.org/10.1186/s12934-025-02652-wStreptomyces sp. KN37Fermentation condition optimizationPlackett-burman designCentral composite design
spellingShingle Xiaoyue Yang
Lijing Yuan
Muhammad Zeeshan
Chuntian Yang
Wen Gao
Guoqiang Zhang
Chunjuan Wang
Optimization of fermentation conditions to increase the production of antifungal metabolites from Streptomyces sp. KN37
Microbial Cell Factories
Streptomyces sp. KN37
Fermentation condition optimization
Plackett-burman design
Central composite design
title Optimization of fermentation conditions to increase the production of antifungal metabolites from Streptomyces sp. KN37
title_full Optimization of fermentation conditions to increase the production of antifungal metabolites from Streptomyces sp. KN37
title_fullStr Optimization of fermentation conditions to increase the production of antifungal metabolites from Streptomyces sp. KN37
title_full_unstemmed Optimization of fermentation conditions to increase the production of antifungal metabolites from Streptomyces sp. KN37
title_short Optimization of fermentation conditions to increase the production of antifungal metabolites from Streptomyces sp. KN37
title_sort optimization of fermentation conditions to increase the production of antifungal metabolites from streptomyces sp kn37
topic Streptomyces sp. KN37
Fermentation condition optimization
Plackett-burman design
Central composite design
url https://doi.org/10.1186/s12934-025-02652-w
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AT lijingyuan optimizationoffermentationconditionstoincreasetheproductionofantifungalmetabolitesfromstreptomycesspkn37
AT muhammadzeeshan optimizationoffermentationconditionstoincreasetheproductionofantifungalmetabolitesfromstreptomycesspkn37
AT chuntianyang optimizationoffermentationconditionstoincreasetheproductionofantifungalmetabolitesfromstreptomycesspkn37
AT wengao optimizationoffermentationconditionstoincreasetheproductionofantifungalmetabolitesfromstreptomycesspkn37
AT guoqiangzhang optimizationoffermentationconditionstoincreasetheproductionofantifungalmetabolitesfromstreptomycesspkn37
AT chunjuanwang optimizationoffermentationconditionstoincreasetheproductionofantifungalmetabolitesfromstreptomycesspkn37