Department of Biological Engineering, College of Engineering, Konkuk University, Seoul 05029, Republic of Korea.
Department of Biological Engineering, College of Engineering, Konkuk University, Seoul 05029, Republic of Korea; Institute for Ubiquitous Information Technology and Applications, Konkuk University, Seoul 05029, Republic of Korea.
Int J Biol Macromol. 2021 Apr 30;177:413-421. doi: 10.1016/j.ijbiomac.2021.02.098. Epub 2021 Feb 17.
Poly(3-hydroxybutyrate) (PHB) is a biobased and biodegradable plastic. Considering the environmental issues of petroleum-based plastics, PHB is promising as it can be degraded in a relatively short time by bacteria to water and carbon dioxide. Substantial efforts have been made to identify PHB-degrading bacteria. To identify PHB-degrading bacteria, solid-based growth or clear zone assays using PHB as the sole carbon source are the easiest methods; however, PHB is difficult to dissolve and distribute evenly, and bacteria grow slowly on PHB plates. Here, we suggest an improved PHB plate assay using cell-grown PHB produced by Halomonas sp. and recovered by sodium dodecyl sulfate (SDS). Preparation using SDS resulted in evenly distributed PHB plates that could be used for sensitive depolymerase activity screening in less time compared with solvent-melted pellet or cell-grown PHB. With this method, we identified 15 new strains. One strain, Cutibacterium sp. SOL05 (98.4% 16S rRNA similarity to Cutibacterium acne), showed high PHB depolymerase activity in solid and liquid conditions. PHB degradation was confirmed by clear zone size, liquid culture, scanning electron microscopy, and Fourier-transform infrared spectroscopy. The results indicate this method can be used to easily identify PHB-degrading bacteria from various sources to strengthen the benefits of bioplastics.
聚 3-羟基丁酸酯(PHB)是一种生物基可生物降解塑料。考虑到石油基塑料带来的环境问题,PHB 具有广阔的应用前景,因为它可以在相对较短的时间内被细菌降解为水和二氧化碳。人们已经做出了大量努力来鉴定 PHB 降解细菌。为了鉴定 PHB 降解细菌,使用 PHB 作为唯一碳源的固体生长或透明带测定法是最简单的方法;然而,PHB 很难溶解和均匀分布,并且 PHB 平板上的细菌生长缓慢。在这里,我们建议使用 Halomonas sp. 产生的细胞生长 PHB 并通过十二烷基硫酸钠(SDS)回收来改进 PHB 平板测定法。使用 SDS 进行制备会导致 PHB 平板均匀分布,与溶剂熔融颗粒或细胞生长 PHB 相比,可用于更灵敏的解聚酶活性筛选,耗时更少。使用该方法,我们鉴定了 15 株新菌株。一株菌株 Cutibacterium sp. SOL05(与 Cutibacterium acne 的 16S rRNA 相似度为 98.4%)在固体和液体条件下均表现出高 PHB 解聚酶活性。通过透明带大小、液体培养、扫描电子显微镜和傅里叶变换红外光谱证实了 PHB 的降解。结果表明,该方法可用于从各种来源中轻松鉴定 PHB 降解细菌,从而增强生物塑料的优势。