Microbial Consortia and Mixed Plastic Waste: Pangenomic Analysis Reveals Potential for Degradation of Multiple Plastic Types via Previously Identified PET Degrading Bacteria.
Microbial Consortia and Mixed Plastic Waste: Pangenomic Analysis Reveals Potential for Degradation of Multiple Plastic Types via Previously Identified PET Degrading Bacteria.
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微生物联合体和混合塑料废物:泛基因组分析揭示了通过先前已确定的PET降解菌降解多种塑料类型的潜力。
DOI:
10.3390/ijms23105612
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发表时间:
2022-05-17
影响因子:
5.6
通讯作者:
中科院分区:
文献类型:
--
作者:
The global utilization of single-use, non-biodegradable plastics, such as bottles made of polyethylene terephthalate (PET), has contributed to catastrophic levels of plastic pollution. Fortunately, microbial communities are adapting to assimilate plastic waste. Previously, our work showed a full consortium of five bacteria capable of synergistically degrading PET. Using omics approaches, we identified the key genes implicated in PET degradation within the consortium’s pangenome and transcriptome. This analysis led to the discovery of a novel PETase, EstB, which has been observed to hydrolyze the oligomer BHET and the polymer PET. Besides the genes implicated in PET degradation, many other biodegradation genes were discovered. Over 200 plastic and plasticizer degradation-related genes were discovered through the Plastic Microbial Biodegradation Database (PMBD). Diverse carbon source utilization was observed by a microbial community-based assay, which, paired with an abundant number of plastic- and plasticizer-degrading enzymes, indicates a promising possibility for mixed plastic degradation. Using RNAseq differential analysis, several genes were predicted to be involved in PET degradation, including aldehyde dehydrogenases and several classes of hydrolases. Active transcription of PET monomer metabolism was also observed, including the generation of polyhydroxyalkanoate (PHA)/polyhydroxybutyrate (PHB) biopolymers. These results present an exciting opportunity for the bio-recycling of mixed plastic waste with upcycling potential.
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影响因子:
13.6
作者:
Geyer R;Jambeck JR;Law KL
通讯作者:
Law KL
影响因子:
5.2
作者:
Bonifer, Kyle S.;Wen, Xianfang;Reynolds, Todd B.
通讯作者:
Reynolds, Todd B.
影响因子:
3
作者:
Chen S;Huang T;Zhou Y;Han Y;Xu M;Gu J
通讯作者:
Gu J
影响因子:
6.4
作者:
Gambarini V;Pantos O;Kingsbury JM;Weaver L;Handley KM;Lear G
通讯作者:
Lear G
影响因子:
6.4
作者:
Blaustein, Ryan A.;McFarland, Alexander G.;Hartmann, Erica M.
通讯作者:
Hartmann, Erica M.