{"title":"Highly efficient degradation of polybutylene succinate (PBS) and polycaprolactone (PCL) by a recombinant marine fungal cutinase.","authors":"Fengjuan Lang, Fan Fei, Chaomin Sun, Shimei Wu","doi":"10.1128/aem.00833-25","DOIUrl":null,"url":null,"abstract":"<p><p>Biodegradable plastics, such as polybutylene succinate (PBS) and polycaprolactone (PCL), pose potential ecological risks due to their slow degradation rates in natural environments. Therefore, there is an urgent need to develop efficient enzymatic degradation technologies for the end-of-life management of PBS and PCL. In this study, we identified a marine fungal cutinase, <i>Aa</i>Cut10, which exhibits significant degradation activity on PBS and PCL films under mild conditions. <i>Aa</i>Cut10 can achieve degradation rates of 26.33% for PBS and 85.67% for PCL films within 20 min at 37°C, corresponding to degradation efficiencies of 315.96 kg PBS·(mol <i>Aa</i>Cut10·h)⁻¹ and 1028.04 kg PCL·(mol <i>Aa</i>Cut10·h)⁻¹, respectively. Notably, <i>Aa</i>Cut10 showed even higher degradation efficiency on PBS and PCL emulsions, achieving degradation rates of 81.88% for PBS and 99.45% for PCL after just 1 min at room temperature. Product analysis showed that <i>Aa</i>Cut10 degrades PBS into monomers and dimers and completely degrades PCL into monomers. The optimal degradation temperature for <i>Aa</i>Cut10 was 23°C for both PBS and PCL. Even at 4°C, <i>Aa</i>Cut10 retained high degradation activity, with relative activities of 60.58% for PBS emulsion and 81.41% for PCL emulsion. Additionally, Ca<sup>2+</sup>, Mg<sup>2+</sup>, and Mn<sup>2+</sup> significantly enhanced the degradation activity of <i>Aa</i>Cut10, and the enzyme remained stable in the presence of chemicals such as methanol, ethanol, and glycerol. Finally, we identified that the amino acids Leu209 and Leu216 in <i>Aa</i>Cut10 play key roles in its degradation functions toward both PBS and PCL.IMPORTANCEAlthough biodegradable plastics can be degraded, their degradation rates in natural environments are slower than expected. To address this issue, we identified a marine fungal cutinase, <i>Aa</i>Cut10, which efficiently degrades various polyesters, including PBS and PCL, into their corresponding monomers, thereby facilitating subsequent recycling and remanufacturing. Notably, <i>Aa</i>Cut10 achieves maximum degradation efficiency at ambient temperature (23°C) and retains high activity even at 4°C, meeting the energy efficiency requirements of industrial applications. Furthermore, <i>Aa</i>Cut10 exhibits high stability in the presence of chemicals, making it suitable for multiphase catalytic systems while the enhancing effects of metal ions on its activity provide tunable targets for process optimization. The catalytic properties of <i>Aa</i>Cut10 not only establish a theoretical framework for designing high-performance degrading enzymes but also offer essential support for developing eco-friendly plastic recycling systems.</p>","PeriodicalId":8002,"journal":{"name":"Applied and Environmental Microbiology","volume":" ","pages":"e0083325"},"PeriodicalIF":3.7000,"publicationDate":"2025-09-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12442398/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Applied and Environmental Microbiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1128/aem.00833-25","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/8/14 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Biodegradable plastics, such as polybutylene succinate (PBS) and polycaprolactone (PCL), pose potential ecological risks due to their slow degradation rates in natural environments. Therefore, there is an urgent need to develop efficient enzymatic degradation technologies for the end-of-life management of PBS and PCL. In this study, we identified a marine fungal cutinase, AaCut10, which exhibits significant degradation activity on PBS and PCL films under mild conditions. AaCut10 can achieve degradation rates of 26.33% for PBS and 85.67% for PCL films within 20 min at 37°C, corresponding to degradation efficiencies of 315.96 kg PBS·(mol AaCut10·h)⁻¹ and 1028.04 kg PCL·(mol AaCut10·h)⁻¹, respectively. Notably, AaCut10 showed even higher degradation efficiency on PBS and PCL emulsions, achieving degradation rates of 81.88% for PBS and 99.45% for PCL after just 1 min at room temperature. Product analysis showed that AaCut10 degrades PBS into monomers and dimers and completely degrades PCL into monomers. The optimal degradation temperature for AaCut10 was 23°C for both PBS and PCL. Even at 4°C, AaCut10 retained high degradation activity, with relative activities of 60.58% for PBS emulsion and 81.41% for PCL emulsion. Additionally, Ca2+, Mg2+, and Mn2+ significantly enhanced the degradation activity of AaCut10, and the enzyme remained stable in the presence of chemicals such as methanol, ethanol, and glycerol. Finally, we identified that the amino acids Leu209 and Leu216 in AaCut10 play key roles in its degradation functions toward both PBS and PCL.IMPORTANCEAlthough biodegradable plastics can be degraded, their degradation rates in natural environments are slower than expected. To address this issue, we identified a marine fungal cutinase, AaCut10, which efficiently degrades various polyesters, including PBS and PCL, into their corresponding monomers, thereby facilitating subsequent recycling and remanufacturing. Notably, AaCut10 achieves maximum degradation efficiency at ambient temperature (23°C) and retains high activity even at 4°C, meeting the energy efficiency requirements of industrial applications. Furthermore, AaCut10 exhibits high stability in the presence of chemicals, making it suitable for multiphase catalytic systems while the enhancing effects of metal ions on its activity provide tunable targets for process optimization. The catalytic properties of AaCut10 not only establish a theoretical framework for designing high-performance degrading enzymes but also offer essential support for developing eco-friendly plastic recycling systems.
生物降解塑料,如聚丁二酸丁二酯(PBS)和聚己内酯(PCL),由于其在自然环境中的降解速度缓慢,造成了潜在的生态风险。因此,迫切需要开发有效的酶降解技术,用于PBS和PCL的生命终止管理。在这项研究中,我们鉴定了一种海洋真菌角质酶AaCut10,它在温和条件下对PBS和PCL薄膜表现出显著的降解活性。在37℃条件下,AaCut10在20分钟内对PBS膜的降解率为26.33%,对PCL膜的降解率为85.67%,对应的降解效率分别为315.96 kg PBS·(mol AaCut10·h)⁻¹和1028.04 kg PCL·(mol AaCut10·h)⁻¹。值得注意的是,AaCut10对PBS和PCL乳剂的降解效率更高,在室温下仅1 min,对PBS和PCL的降解率分别达到81.88%和99.45%。产物分析表明,AaCut10将PBS降解为单体和二聚体,将PCL完全降解为单体。AaCut10对PBS和PCL的最佳降解温度均为23℃。即使在4°C时,AaCut10仍保持较高的降解活性,对PBS乳液的相对活性为60.58%,对PCL乳液的相对活性为81.41%。此外,Ca2+、Mg2+和Mn2+显著增强了AaCut10的降解活性,并且该酶在甲醇、乙醇和甘油等化学物质存在下保持稳定。最后,我们发现AaCut10中的氨基酸Leu209和Leu216在其对PBS和PCL的降解功能中起关键作用。尽管生物可降解塑料可以降解,但它们在自然环境中的降解速度比预期的要慢。为了解决这个问题,我们发现了一种海洋真菌角质酶AaCut10,它可以有效地降解各种聚酯,包括PBS和PCL,从而促进随后的回收和再制造。值得注意的是,AaCut10在环境温度(23°C)下达到最大的降解效率,即使在4°C下也保持高活性,满足工业应用的能效要求。此外,AaCut10在化学物质存在下表现出高稳定性,使其适用于多相催化系统,而金属离子对其活性的增强作用为工艺优化提供了可调的目标。AaCut10的催化性能不仅为设计高性能降解酶提供了理论框架,而且为开发环保塑料回收系统提供了必要的支持。
期刊介绍:
Applied and Environmental Microbiology (AEM) publishes papers that make significant contributions to (a) applied microbiology, including biotechnology, protein engineering, bioremediation, and food microbiology, (b) microbial ecology, including environmental, organismic, and genomic microbiology, and (c) interdisciplinary microbiology, including invertebrate microbiology, plant microbiology, aquatic microbiology, and geomicrobiology.