{"title":"Untargeted metabolomics profiling reveals carbon source-dependent rhamnolipid congener production in Burkholderia thailandensis E264","authors":"Nadirah Arifin , Kamalrul Azlan Azizan , Zainatul 'Asyiqin Samsu","doi":"10.1016/j.jbiotec.2025.07.014","DOIUrl":null,"url":null,"abstract":"<div><div>This study investigated glycerol and oleic acid as carbon sources on RL production and congener diversity in <em>Burkholderia thailandensis</em> E264 (BSL 1), a safer alternative to <em>Pseudomonas aeruginosa,</em> using an untargeted metabolomic approach. <em>B. thailandensis</em> E264 was grown in triplicate for nine days at 30 °C, extracted using ethyl acetate, and analysed using LC/Q-TOF/MS. Results showed 84 RL congeners with different adducts were annotated. Cultures with glycerol primarily produced di-RLs with carbon chain lengths from C<sub>12:2</sub> to C<sub>16</sub>-C<sub>14</sub>, whereas cultures with oleic acid produced mono-RLs (C<sub>8:2</sub> to C<sub>16</sub>-C<sub>16</sub>). Multivariate analysis of PLS-DA revealed distinct RL profiles in response to different carbon sources, with di-RL-C<sub>10</sub>-C<sub>12</sub> (VIP = 2.15) and mono-RL-C<sub>10</sub>-C<sub>14:1</sub> (VIP = 1.90) identified as key congeners in the glycerol and oleic acid cultures, respectively. The heatmap highlighted significant fold changes in RL congener abundance (2.94-fold higher di-RL-C<sub>14</sub> in glycerol culture and 4.38-fold higher mono-RL-C<sub>8</sub>-C<sub>10</sub> in oleic acid culture). These findings demonstrate that the carbon source significantly affects RL congener production in <em>B. thailandensis</em> E264, suggesting the potential for RL production optimisation and tailoring congener profiles for specific applications.</div></div>","PeriodicalId":15153,"journal":{"name":"Journal of biotechnology","volume":"406 ","pages":"Pages 211-224"},"PeriodicalIF":3.9000,"publicationDate":"2025-07-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of biotechnology","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0168165625001853","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
This study investigated glycerol and oleic acid as carbon sources on RL production and congener diversity in Burkholderia thailandensis E264 (BSL 1), a safer alternative to Pseudomonas aeruginosa, using an untargeted metabolomic approach. B. thailandensis E264 was grown in triplicate for nine days at 30 °C, extracted using ethyl acetate, and analysed using LC/Q-TOF/MS. Results showed 84 RL congeners with different adducts were annotated. Cultures with glycerol primarily produced di-RLs with carbon chain lengths from C12:2 to C16-C14, whereas cultures with oleic acid produced mono-RLs (C8:2 to C16-C16). Multivariate analysis of PLS-DA revealed distinct RL profiles in response to different carbon sources, with di-RL-C10-C12 (VIP = 2.15) and mono-RL-C10-C14:1 (VIP = 1.90) identified as key congeners in the glycerol and oleic acid cultures, respectively. The heatmap highlighted significant fold changes in RL congener abundance (2.94-fold higher di-RL-C14 in glycerol culture and 4.38-fold higher mono-RL-C8-C10 in oleic acid culture). These findings demonstrate that the carbon source significantly affects RL congener production in B. thailandensis E264, suggesting the potential for RL production optimisation and tailoring congener profiles for specific applications.
期刊介绍:
The Journal of Biotechnology has an open access mirror journal, the Journal of Biotechnology: X, sharing the same aims and scope, editorial team, submission system and rigorous peer review.
The Journal provides a medium for the rapid publication of both full-length articles and short communications on novel and innovative aspects of biotechnology. The Journal will accept papers ranging from genetic or molecular biological positions to those covering biochemical, chemical or bioprocess engineering aspects as well as computer application of new software concepts, provided that in each case the material is directly relevant to biotechnological systems. Papers presenting information of a multidisciplinary nature that would not be suitable for publication in a journal devoted to a single discipline, are particularly welcome.