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A hydrophobic SPG (shirasu porous glass) membrane-aerated biofilm reactor (MABR) with genetically engineered microorganism (GEM) biofilm formed on the SPG membrane surface was applied to treat atrazine wastewater. The contaminant removal performance and its influencing factors were investigated during the stable operation of this MABR. The results indicated that the oxygen supply capacity could be increased in the SPG membrane aeration when the membrane pore size and the aeration pressure increased, which could improve the performance of COD and atrazine removals. The maximum oxygen supply capacity of hydrophobic SPG membrane with pore size of 1.5 μm was estimated to be about 22.4 g·(m·d) at aeration pressure of 70 kPa. When aeration pressure was 70 kPa and hydraulic retention time (HRT) was 1.5 h, the average COD removal efficiency was 80.1% and the average organic loading rate removed was 1.86 kg·(m·d)in the MABR with 1.5 μm hydrophobic SPG membrane. Under the same operating conditions, the average atrazine removal efficiency was 62.5% and the average atrazine loading rate removed was 0.18 kg·(m·d). The COD and atrazine removal efficiencies decreased significantly at further shortened HRT and increased influent organic loading rate. DO concentration showed more significant influence on atrazine removal. The simplex genetically engineered microorganism biofilm turned into complex microbial community gradually during MABR operation, but the GEM cells could still reside in the biofilm well. Therefore, the efficient atrazine removal by GEM bioaugmentation could be maintained.
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http://dx.doi.org/10.13277/j.hjkx.2016.08.035 | DOI Listing |
Proc Natl Acad Sci U S A
July 2025
Department of Cell Biology, School of Medicine, Johns Hopkins University, Baltimore, MD 21205.
FtsZ, the tubulin-like GTPase, is the central organizer of the bacterial divisome, a macromolecular complex that synthesizes new septal cell wall (made of septal peptidoglycan, sPG) to allow cell wall constriction and cytokinesis. In , it was shown that 1) FtsZ recruits all essential divisome proteins to the septum, including the core sPG synthase complex, FtsWIQLB, and its activator, FtsN; 2) FtsWIQLB must complex with FtsN to be activated to synthesize sPG under the wildtype background; and 3) the Brownian ratcheting by treadmilling FtsZ polymers drives the directional movements of sPG synthase proteins along the septum circumference; and 4) FtsZ is essential for the early stage, but dispensable for the late stage of cell wall constriction. However, it remains unclear how FtsZ spatial-temporally organizes the divisome for robust cell wall constriction during cytokinesis.
View Article and Find Full Text PDFJ Membr Biol
June 2025
Biosciences and Bioengineering Division, CSIR-National Institute for Interdisciplinary Science and Technology (NIIST), Trivandrum, Kerala, 695019, India.
Nat Microbiol
June 2025
Department of Biophysics and Biophysical Chemistry, Johns Hopkins School of Medicine, Baltimore, MD, USA.
In Escherichia coli, FtsN is thought to coordinate septal peptidoglycan (sPG) synthesis and degradation. Its E domain interacts with the sPG synthesis complex, FtsWIQLB, and its SPOR domain interacts with denuded glycan (dnG), intermediates of sPG degradation. Here we used single-molecule tracking of FtsN and FtsW to investigate how FtsN coordinates the two opposing processes.
View Article and Find Full Text PDFOphthalmol Retina
April 2025
Department of Ophthalmology, CHU Nantes, Nantes University, Nantes, France; Clinical Investigation Center CIC1413, CHU Nantes, INSERM, Nantes University, Nantes, France. Electronic address:
Purpose: The aim of this study was to identify predictive factors for spontaneous internal limiting membrane (ILM) peeling after idiopathic unilateral epiretinal membrane (ERM) removal and to compare outcomes between patients with and without spontaneous ILM peeling.
Design: The PEELING study was a national randomized clinical trial.
Participants: Patients with symptomatic idiopathic ERM were recruited from 5 ophthalmology departments.
CNS Neurosci Ther
April 2025
Division of Cancer Stem Cells and Cardiovascular Regeneration, Manipal Institute of Regenerative Medicine, Manipal Academy of Higher Education (MAHE), Bangalore, India.
Main Problem: The mechanism behind Parkinson's disease (PD) is still unclear, and a cure to stop its progression is yet to be found. This is mainly due to the lack of effective human PD models. To address this, we generated an in vitro PD model using Wharton's jelly-derived mesenchymal stem cells (WJMSCs).
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