Abstract

Gravity-driven membrane (GDM) ultrafiltration systems require little maintenance: they operate without electricity at ultra-low pressure in dead-end mode and without control of the biofilm formation. These systems are already in use for water purification in some regions of the world where adequate treatment and distribution of drinking water is not readily available. However, many water bodies worldwide exhibit harmful blooms of cyanobacteria that severely lower the water quality due to the production of toxic microcystins (MCs). We studied the performance of a GDM system during an artificial Microcystis aeruginosa bloom in lake water and its simulated collapse (i.e., the massive release of microcystins) over a period of 21 days. Presence of live or destroyed cyanobacterial cells in the feed water decreased the permeate flux in the Microcystis treatments considerably. At the same time, the microbial biofilms on the filter membranes could successfully reduce the amount of microcystins in the filtrate below the critical threshold concentration of 1 µg L−1 MC for human consumption in three out of four replicates after 15 days. We found pronounced differences in the composition of bacterial communities of the biofilms on the filter membranes. Bacterial genera that could be related to microcystin degradation substantially enriched in the biofilms amended with microcystin-containing cyanobacteria. In addition to bacteria previously characterized as microcystin degraders, members of other bacterial clades potentially involved in MC degradation could be identified.

Highlights

  • During the last century, the anthropogenic input of nutrients into freshwaters has resulted in a distinct increase of cyanobacterial biomass in many water bodies worldwide [1]

  • Some cyanobacteria represent a major challenge for drinking water usage due to their production of microcystins (MCs), toxic secondary metabolites that affect a wide range of animals and humans [3]

  • The cell number of the cyanobacterial culture was determined by flow cytometry, and the MC concentration was quantified by high-performance liquid-chromatography (HPLC) as followed: A volume of 5 mL of the culture was frozen at 223uC for three hours

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Summary

Introduction

The anthropogenic input of nutrients into freshwaters has resulted in a distinct increase of cyanobacterial biomass in many water bodies worldwide [1]. Some cyanobacteria represent a major challenge for drinking water usage due to their production of microcystins (MCs), toxic secondary metabolites that affect a wide range of animals and humans [3]. The major route of human exposure to MCs is via oral ingestion, mainly due to the consumption of drinking water [4]. Microcystis aeruginosa is known to form massive blooms in many lakes worldwide, and it produces MCs in high amounts. The concentrations of the intracellular MCs range between 0.3 to 15 mg L21 [6] and up to 400 mg L21 [7] in cyanobacterial blooms, occasionally high concentrations of up to 1400 mg L21 were found [8]. Elimination of the MCs from drinking water is highly desirable

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