Zhao Yimeng, Zhang Jun, Ni Min, Pan Yang, Li Lu, Ding Yanyan
School of Environmental Science and Engineering, Suzhou University of Science and Technology, Suzhou 215009, China.
Suzhou Drainage Company Limited, Suzhou 215009, China.
Sci Total Environ. 2024 Jun 10;928:172408. doi: 10.1016/j.scitotenv.2024.172408. Epub 2024 Apr 10.
This study investigated the mechanisms of microbial growth and metabolism during biofilm cultivation in the biofilm sequencing batch reactor (BSBR) process for phosphate (P) enrichment. The results showed that the sludge discharge was key to biofilm growth, as it terminated the competition for carbon (C) source between the nascent biofilm and the activated sludge. For the tested reactor, after the sludge discharge on 18 d, P metabolism and C source utilization improved significantly, and the biofilm grew rapidly. The P concentration of the recovery liquid reached up to 157.08 mg/L, which was sufficient for further P recovery via mineralization. Meta-omics methods were used to analyze metabolic pathways and functional genes in microbial growth during biofilm cultivation. It appeared that the sludge discharge activated the key genes of P metabolism and inhibited the key genes of C metabolism, which strengthened the polyphosphate-accumulating metabolism (PAM) as a result. The sludge discharge not only changed the types of polyphosphate-accumulating organisms (PAOs) but also promoted the growth of dominant PAOs. Before the sludge discharge, the necessary metabolic abilities that were spread among different microorganisms gradually concentrated into a small number of PAOs, and after the sludge discharge, they further concentrated into Candidatus_Contendobacter (P3) and Candidatus_Accumulibacter (P17). The messenger molecule C-di-GMP, produced mostly by P3 and P17, facilitated P enrichment by regulating cellular P and C metabolism. The glycogen-accumulating organism (GAO) Candidatus_Competibacter secreted N-Acyl homoserine lactones (AHLs), which stimulated the secretion of protein in extracellular polymeric substances (EPS), thus promoting the adhesion of microorganisms to biofilm and improving P metabolism via EPS-based P adsorption. Under the combined action of the dominant GAOs and PAOs, AHLs and C-di-GMP mediated QS to promote biofilm development and P enrichment. The research provides theoretical support for the cultivation of biofilm and its wider application.
本研究调查了在生物膜序批式反应器(BSBR)工艺中进行磷(P)富集时生物膜培养过程中微生物生长和代谢的机制。结果表明,排泥是生物膜生长的关键,因为它终止了新生生物膜与活性污泥之间对碳(C)源的竞争。对于测试的反应器,在第18天排泥后,P代谢和C源利用显著改善,生物膜迅速生长。回收液中的P浓度高达157.08mg/L,足以通过矿化进一步回收P。采用宏组学方法分析生物膜培养过程中微生物生长的代谢途径和功能基因。结果表明,排泥激活了P代谢的关键基因,抑制了C代谢的关键基因,从而强化了聚磷积累代谢(PAM)。排泥不仅改变了聚磷积累生物体(PAOs)的类型,还促进了优势PAOs的生长。排泥前,分布在不同微生物中的必要代谢能力逐渐集中到少数PAOs中,排泥后,它们进一步集中到“候选竞争杆菌”(P3)和“候选聚磷菌”(P17)中。主要由P3和P17产生的信使分子环二鸟苷酸(c-di-GMP)通过调节细胞内P和C代谢促进P富集。糖原积累生物体(GAO)“候选竞争杆菌”分泌N-酰基高丝氨酸内酯(AHLs),刺激细胞外聚合物(EPS)中蛋白质的分泌,从而促进微生物对生物膜的附着,并通过基于EPS的P吸附改善P代谢。在优势GAOs和PAOs的共同作用下,AHLs和c-di-GMP介导群体感应以促进生物膜发育和P富集。该研究为生物膜的培养及其更广泛的应用提供了理论支持。