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Improvement of polyhydroxybutyrate (PHB) plate-based screening method for PHB degrading bacteria using cell-grown amorphous PHB and recovered by sodium dodecyl sulfate (SDS)

Authors
Park, Sol LeeCho, Jang YeonChoi, Tae-RimSong, Hun-SukBhatia, Shashi KantGurav, RanjitPark, See-HyoungPark, KyungmoonJoo, Jeong ChanHwang, Sung YeonYang, Yung-Hun
Issue Date
30-Apr-2021
Publisher
ELSEVIER
Keywords
Poly(3-hydroxybutyrate); Degradation; Screening
Citation
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, v.177, pp.413 - 421
Journal Title
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
Volume
177
Start Page
413
End Page
421
URI
https://scholarworks.bwise.kr/hongik/handle/2020.sw.hongik/15545
DOI
10.1016/j.ijbiomac.2021.02.098
ISSN
0141-8130
Abstract
Poly(3-hydroxybutyrate) (PHB) isa 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. (c) 2021 Elsevier B.V. All rights reserved.
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