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Although long-term studies on enhanced biological phosphorus removal systems and biofilm-based phosphorus enrichment processes have established the crucial involvement of extracellular polymeric substances (EPS), the mechanisms by which EPS participate in phosphorus uptake and release remain debated. Key points of contention include whether EPS exhibit independent phosphorus sequestration and release capabilities distinct from cellular metabolic activities, and whether biochemical reactions or physico-chemical precipitation processes dominate within EPS. This review summarizes major findings from previous research on phosphorus uptake and release mechanisms mediated by EPS. Based on the transport and transformation behavior of phosphorus and its compounds in environmental systems, as well as critical phenomena recently observed in sequencing batch biofilm reactors for phosphorus removal and enrichment, a new hypothesis is proposed: under redox-regulated conditions, the dominant mechanism of EPS in biological phosphorus cycling involves physico-chemical processes of binding/fixation and dissociation/mobilization, while phosphorus migration between EPS and the aqueous phase is primarily diffusion-driven. This hypothesis offers an integrated framework for explaining phosphorus translocation and transformation between EPS and the solution, helps to reconcile existing controversies and unanswered questions in the literature, and provides a novel theoretical basis for understanding the role of EPS in biological phosphorus removal processes.
, authors=Zhen BI
1, 2, Ge SONG
1, Yong HUANG
1, 2, *, authorsList=Zhen BI, Ge SONG, Yong HUANG, authorCompany=null, correspAuthors=Yong HUANG, authorNote=null, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=null, pdfFileSize=null, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=null, mapNumber=null, fund=null), CN=ArticleExt(id=1314918489190658406, articleId=1314918487231918436, tenantId=1146029695717560320, journalId=1234093305789726721, language=CN, title=胞外聚合物在吸磷/释磷过程中的作用机制, columnId=1234106386565624579, journalTitle=中国环境科学, columnName=水污染与控制, runingTitle=null, highlight=null, articleAbstract=
尽管生物除磷系统和生物膜磷富集系统的长期研究结果已证实了胞外聚合物(EPS)的重要作用,然而对其在吸磷/释磷过程中的作用机制,尤其是围绕EPS是否具有独立于细胞吸磷/释磷的能力,以及EPS中是发生生物化学反应还是物理化学沉淀作用这两方面尚存在争议.本文综述了现有EPS吸磷/释磷作用机制相关研究的主要成果,并基于磷及其化合物在环境中的迁移转化特性,结合近年来在序批式生物膜去除富集磷系统中所观察到的重要现象,对EPS吸磷/释磷作用机制提出了新的假说:即氧化还原条件调控下,磷的结合/固定与离解/迁移的物理化学过程,是EPS在生物吸磷/释磷过程中的主导性作用机制,而磷在EPS与溶液间的迁移过程主要受扩散的支配.利用新假说,可以清晰地描述磷在EPS与溶液间的迁移转化过程,澄清文献中的相关争议和质疑,为阐释生物除磷过程中EPS的作用提供了新的理论视角.
, authors=毕贞
1, 2, 宋歌
1, 黄勇
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毕贞(1986-),女,江苏苏州人,副教授,博士,研究方向为污水处理与资源化利用技术.发表论文30余篇.bizhen@mail.usts.edu.cn.
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毕贞(1986-),女,江苏苏州人,副教授,博士,研究方向为污水处理与资源化利用技术.发表论文30余篇.bizhen@mail.usts.edu.cn.
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