Grafted glycopolymer-based receptor mimics on polymer support for selective adhesion of bacteria.

A sugar-containing monomer (2-lactobionamidoethyl methacrylate, LAMA) was grafted on a polypropylene (PP) microfiltration membrane surface by UV-induced graft copolymerization. The degree of grafting can be controlled by variation of monomer concentration, UV irradiation time, and photoinitiator concentration. Fourier transform infrared spectroscopy and scanning electron microscopy were employed to confirm the surface modification on the membranes. The water contact angle was used to evaluate the hydrophilicity change of the membrane surface before and after modification. Bacteria capture experiments showed that the membrane could selectively bind E. faecalis while adhesion of S. maltophilia was not influenced by the functionalization of PP with grafted poly(LAMA). The adhesion of E. faecalis onto poly(LAMA) grafted membrane could be inhibited by 200 mM galactose solution; however, glucose solution showed no inhibition effect. Moreover, occupying sugar residues on the membrane surface primarily by a galactose targeting lectin, peanut agglutinin, could significantly suppress the following adhesion of E. faecalis. All these results clearly demonstrate that this poly(LAMA) grafted PP membrane can selectively capture E. faecalis and that this selection is based on the interaction between galactose side groups on grafted flexible functional polymer chains on the membrane surface and galactose binding protein on the E. faecalis cell membrane.

Effects of electric polarization of indium tin oxide (ITO) and polypyrrole on biofilm formation.

The influence of electric polarization on primary adhesion and on biofilm formation was investigated. As substrata, indium tin oxide (ITO) and polypyrrole coatings were used because of their electric conductivity. The materials were polarized from -600 mV to +600 mV, switching every 60 seconds. Control was non-polarized substrata. Primary adhesion under this regime was not strongly influenced, however, the morphology of the primary biofilm was obviously different from that of the control. Biofilm formation of the natural population of non-chlorinated drinking water, supplemented with nutrient in low concentration, was determined over 164 hours. While the biofilm on the control surface developed to a thickness of about 100 microm, on the pulsed polarized surface it reproducibly developed only to a very thin biofilm. Faster switching of the polarization (10 second) had no further influence. If the polarization routine was reduced to only twice a day (one hour), no influence on biofilm development was observed. These results indicate that fluctuating polarization at a rate of once per minute inhibits the physiological processes during biofilm formation during one week. Investigations are in process to determine further details of this effect in order to employ it for inhibition of biofouling.

Biofilm growth in response to various concentrations of biodegradable material in drinking water.

Biological stability is one of the most important aspects of safe drinking water. It depends crucially on the availability of biodegradable organic carbon (BDOC). Measurement of BDOC is time-consuming and only performed if an increase is suspected. In this study, a fibre optical sensor (FOS) was used to detect changes in BDOC, detected as an increase in biofilm growth. The FOS consists of a sending and a receiving optical fibre, the latter connected to a detector. When material is deposited at the tip of the fibre, an increase of backscattered light is detected. In a system fed with drinking water, the signal was correlated to biofilm growth which was confirmed by independent surface colonisation determination. When 1 and 3mgL(-1) of BDOC respectively was added, the increment of the FOS signal over a period of 1 week could be distinguished. Interference by planktonic components and humic substances could be excluded. The biofilm on the FOS could be used as a means to detect changes in BDOC in drinking water and the signal has an early warning capacity.

Establishment of HPC(R2A) for regrowth control in non-chlorinated distribution systems.

Drinking water distributed without disinfection and without regrowth problems for many years may show bacterial regrowth when the residence time and/or temperature in the distribution system increases or when substrate and/or bacterial concentration in the treated water increases. An example of a regrowth event in a major German city is discussed. Regrowth of HPC bacteria occurred unexpectedly at the end of a very hot summer. No pathogenic or potentially pathogenic bacteria were identified. Increased residence times in the distribution system and temperatures up to 25 degrees C were identified as most probable causes and the regrowth event was successfully overcome by changing flow regimes and decreasing residence times. Standard plate counts of HPC bacteria using the spread plate technique on nutrient rich agar according to German Drinking Water Regulations (GDWR) had proven to be a very good indicator of hygienically safe drinking water and to demonstrate the effectiveness of water treatment. However, the method proved insensitive for early regrowth detection. Regrowth experiments in the lab and sampling of the distribution system during two summers showed that spread plate counts on nutrient-poor R2A agar after 7-day incubation yielded 100 to 200 times higher counts. Counts on R2A after 3-day incubation were three times less than after 7 days. As the precision of plate count methods is very poor for counts less than 10 cfu/plate, a method yielding higher counts is better suited to detect upcoming regrowth than a method yielding low counts. It is shown that for the identification of regrowth events HPC(R2A) gives a further margin of about 2 weeks for reaction before HPC(GDWR).

Contamination of drinking water by coliforms from biofilms grown on rubber-coated valves.

In water samples from drinking water distribution systems, coliform bacteria (predominantly Citrobacter species) were repeatedly detected. Disinfection and flushing of the systems did not erase the problem. The pattern of the coliform occurrences indicated contamination originating from biofilms. After inspection of internal surfaces of the systems, no significant biofilm growth was observed on pipe surfaces, but in a number of cases, visible biofilms were detected on rubber-coated valves which harboured the same coliform species as those found in the drinking water samples. In these cases, the rubber-coated valves seemed to act as point sources for the contamination of water.