College of Biological, Chemical Science and Engineering, Jiaxing University, Jiaxing, 314001, PR China.
College of Biological, Chemical Science and Engineering, Jiaxing University, Jiaxing, 314001, PR China.
J Environ Manage. 2022 Nov 1;321:115950. doi: 10.1016/j.jenvman.2022.115950. Epub 2022 Aug 18.
In this study, the salt-tolerant aerobic granular sludge (SAGS) was cultivated with the increased salinity (0-9% NaCl), showing oval shape, and clear outline. The related sludge characteristics in the formation process of SAGS as well as the effects of salinity on the performance (removal ability, sludge biomass and EPS component) of SAGS were evaluated. Increased salinity accelerated the formation of SAGS, and resulted in the excess secretion of EPS. Relationship between EPS and settling capacity of SAGS was determined, with the increase of salinity, SVI decreased linearly and the sedimentation performance of granular sludge was enhanced. Pearson correlation analysis showed that shorter settling time (3 min) and longer anaerobic influent time (30 min) were beneficial to the operation of SAGS reactor. Metagenomics results showed that the SAGS was dominated by Candida, Halomonas and other salt-tolerant bacteria, the enrichment of these salt-tolerant microbes played an important role in maintaining the stability of granular sludge system and improving the overall salt-tolerant performance. Compared with S9 samples, the proteome regulation in S0 sample was more active and the abundance of Cell motility related proteins was 5 times higher than that in S9 samples. Extracellular structure related proteins was more active in S9, and its abundance was 3.6 times that of S0.
在本研究中,采用逐步提高盐度(0-9% NaCl)的方法培养了耐盐好氧颗粒污泥(SAGS),其呈现出椭圆形,轮廓清晰。评估了 SAGS 形成过程中相关污泥特性以及盐度对 SAGS 性能(去除能力、污泥生物量和 EPS 成分)的影响。增加盐度加速了 SAGS 的形成,并导致 EPS 的过度分泌。确定了 EPS 与 SAGS 沉降性能之间的关系,随着盐度的增加,SVI 线性下降,颗粒污泥的沉降性能得到增强。Pearson 相关性分析表明,较短的沉降时间(3 分钟)和较长的厌氧进水时间(30 分钟)有利于 SAGS 反应器的运行。宏基因组学结果表明,SAGS 主要由 Candida、Halomonas 等耐盐细菌组成,这些耐盐微生物的富集对维持颗粒污泥系统的稳定性和提高整体耐盐性能起着重要作用。与 S9 样品相比,S0 样品的蛋白质组调节更为活跃,细胞运动相关蛋白的丰度比 S9 样品高 5 倍。S9 中细胞外结构相关蛋白更为活跃,其丰度是 S0 的 3.6 倍。