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Allelic replacement mutants were constructed within arginine deiminase (arcA1 and arcA2) to assess the function of the arginine deiminase (ADI) pathway in organic acid resistance and biofilm formation of Staphylococcus epidermidis 1457. A growth-dependent acidification assay (pH ∼5.0 to ∼5.2) determined that strain 1457 devoid of arginine deiminase activity (1457 ΔADI) was significantly less viable than the wild type following depletion of glucose and in the presence of arginine. However, no difference in viability was noted for individual 1457 ΔarcA1 (native) or ΔarcA2 (arginine catabolic mobile element [ACME]-derived) mutants, suggesting that the native and ACME-derived ADIs are compensatory in S. epidermidis. Furthermore, flow cytometry and electron paramagnetic resonance spectroscopy results suggested that organic acid stress resulted in oxidative stress that could be partially rescued by the iron chelator dipyridyl. Collectively, these results suggest that formation of hydroxyl radicals is partially responsible for cell death via organic acid stress and that ADI-derived ammonia functions to counteract this acid stress. Finally, static biofilm assays determined that viability, ammonia synthesis, and pH were reduced in strain 1457 ΔADI following 120 h of growth in comparison to strain 1457 and the arcA1 and arcA2 single mutants. It is hypothesized that ammonia synthesis via the ADI pathway is important to reduce pH stress in specific microniches that contain high concentrations of organic acids., (Copyright © 2014, American Society for Microbiology. All Rights Reserved.)

In general, conventional activated sludge (ASP) or enhanced biological phosphorus removing (EBPR) sludge has been used as seed culture for developing EBPR sludge and the time reported for development varies from months to year. In the present study cow-dung has been used as seed culture and EBPR sludge was developed within 36 days. The developed EBPR sludge has been used to evaluate the performance of sequential batch reactor (SBR) and sequential batch biofilm reactors (SBBR) for simultaneous nitrogen and phosphorus removal from synthetic wastewater containing glucose as carbon source. Three reactors were operated, SBR-1 containing only suspended biomass, SBBR-2 and SBBR-3 containing 5% and 10% polyurethane foam (PUF) media respectively along with suspended biomass. In all the reactors phosphorus removal was nearly the same and was more than 80%. In all the three reactors greater than 90% nitrification was achieved. Nitrogen removal in SBR-1 was 48% and in SBBR-2 and SBBR-3 it was more than 62%. On line monitoring of oxidation-reduction potential (ORP), pH and phosphorus during a cycle indicated that ORP and pH can be useful for real time control and optimization of the process.

Listeria monocytogenes, an opportunistic food borne pathogen can cause serious infections in immunocompromised individuals. L. monocytogenes is capable of producing biofilm on the surface of food processing lines and instruments.The biofilm transfers contamination to food products and impose risk to public health. In the present study biofilm producing ability of L. monocytogenes isolates were investigated phenotypically and genotypically by microtiter assay and multiplex PCR, respectively. Out of 38 L. monocytogenes isolates 14 were recovered from animal clinical cases, 12 bovine environment and 12 from milk samples. A total of 3 (21.42%) clinical, 2 (16.66%) environment and 3 (25%) milk samples respectively, revealed biofilm production in microtiter assay. Cumulative results showed that 23 (60.52%) out of 38 strains of L. monocytogenes were positive for luxS and flaA gene and 1 (2.63%) was positive only for the flaA gene. [ABSTRACT FROM AUTHOR]