The aim of this study was to evaluate bacterial and fungal aerosol concentrations at the holy mosque (Al-Masjid Al-Haram). Air samples were collected from different locations inside and outside the holy mosque, during the month of Ramadan-2011 (the fasting month), using a portable Air-port MD8 gelatin filter sampler. Trypticase soya agar and Capek's dox agar media were used to count bacteria and fungi, respectively. The mean concentrations of airborne bacteria and fungi ranged between 105–106 colony forming unit per cubic meter of air (CFU/m3) outside, and ∼102–105 CFU/m3 inside locations. The highest outside bacterial concentrations 106 CFU/m3 were found at the Al Umra, Al Fatah and eastern plazas, and the highest inside fungal concentrations ∼105 CFU/m3 were found at the courtyard, expansion of 1st floor, and roof. Significant differences (P < 0.05) were found between bacterial and fungal concentrations inside and outside sampling locations, higher concentrations shifted towards to outside locations. Significant differences were also found between the bacterial and fungal concentrations inside–unclosed and semi-closed (P < 0.05) with inside-closed locations. Gram-positive bacteria, Bacillus and Micrococcus, and fungi, Aspergillus niger were the dominant microbial aerosol genera. The obtained data is considered a step to make up the gap about airborne microbial contamination inside the holy mosque, and microbial air quality should be studied along over the year at the holy mosque in the future.

Bacterial strains and metagenomic clones, both obtained from petroleum reservoirs, were evaluated for petroleum degradation abilities either individually or in pools using seawater microcosms for 21days. Gas Chromatography–Flame Ionization Detector (GC–FID) and Gas Chromatography-Mass Spectrometry (GC–MS) analyses were carried out to evaluate crude oil degradation. The results showed that metagenomic clones 1A and 2B were able to biodegrade n-alkanes (C14 to C33) and isoprenoids (phytane and pristane), with rates ranging from 31% to 47%, respectively. The bacteria Dietzia maris CBMAI 705 and Micrococcus sp. CBMAI 636 showed higher rates reaching 99% after 21days. The metagenomic clone pool biodegraded these compounds at rates ranging from 11% to 45%. Regarding aromatic compound biodegradation, metagenomic clones 2B and 10A were able to biodegrade up to 94% of phenanthrene and methylphenanthrenes (3-MP, 2-MP, 9-MP and 1-MP) with rates ranging from 55% to 70% after 21days, while the bacteria Dietzia maris CBMAI 705 and Micrococcus sp. CBMAI 636 were able to biodegrade 63% and up to 99% of phenanthrene, respectively, and methylphenanthrenes (3-MP, 2-MP, 9-MP and 1-MP) with rates ranging from 23% to 99% after 21days. In this work, isolated strains as well as metagenomic clones were capable of degrading several petroleum compounds, revealing an innovative strategy and a great potential for further biotechnological and bioremediation applications.

Turbinaria ornata mediated silver nanoparticles (TOAg-NPs) were evaluated for antibacterial activity against 15 biofilm forming bacterial isolates. A field study in natural seawater for 60days showed antifouling activity of TOAg-NPs on stainless steel coupons (SS-304) coated with Apcomin zinc chrome (AZC) primer. Though TOAg-NPs showed broad spectrum of antibacterial activity, the maximum zone of inhibition was with Escherichia coli (71.9%) and a minimum with Micrococcus sp. (40%) due to the EPS secretion from Gram-positive bacteria. Compared to control coupons (18.9 [×103], 67.0 [×103], 13.5 [×104] and 24.7 [×104]CFU/cm2), experimental biocide coupons (71.0 [×102], 32.0 [×103], 82.0 [×103] and 11.3 [×104]CFU/cm2) displayed lesser bacterial population density. Toxicity studies revealed 100% mortality for Balanus amphitrite larvae at 250μgml−1 concentration within 24h, while 56.6% recorded for Artemia marina at the same concentration indicating less toxicity to non target species. It proved that AZC+TOAg-NPs prevent biofouling by its Ag-NS affinity and antimicrobial effectivity.

Oil-degrading bacteria were isolated from waters and sediments of the Manila Bay and Pasig River [Philippines]. Five types of bacteria were isolated from Manila Bay and four from Pasig River. The identified crude oil degrading species are Vibrio sp., Alcaligenes sp., Flavobacterium indologenes and Acinetobacter sp. from Manila Bay, and Pseudomonas aeruginosa, Bacillus sp., Micrococcus sp. and Pseudomonas putida from Pasig River. These isolates were identified through morphological and physiological characterization. The bioremediation potential for each of the isolates was assessed. The percentages oil conversion for the bacterial isolates ranged from 2.99 percent - 53.44 percent in one week's time. Alcaligenes sp. exhibited the highest biodegradation potential for all isolates. Statistical analysis revealed that the mean percentages diesel oil conversion by the isolates were significantly higher than their mean percentages crude oil conversion. Pure and mixed cultures did not give significant differences in their mean percentages crude oil conversion

Levofloxacin (LFX) is a widely used antibiotic medication. Persistent traces of LFX in water and wastewater may induce bacterial resistance. Photon-driven advanced oxidation processes (AOPs) can assist in attaining complete abatement of LFX for environmental protection. This work benchmarks different solar AOPs based on hydroxyl radical (OH•) and sulphate radical (SO₄•⁻) chemistry. Other oxidant precursors, as radical sources, were used to selectively control the generation of either hydroxyl radical (i.e., H₂O₂), sulphate radical (i.e., peroxydisulphate (PDS)), or a controlled mixture ratio of both OH•/SO₄•⁻ (i.e., peroxymonosulphate (PMS)). The influence of pH on degradation performance was evaluated using unbuffered and buffered solutions. Simulated irradiation/PMS process exhibited a strong pH-dependence attaining partial degradation of ca. 56% at pH 5 up to complete degradation at pH 7. Despite the similitudes on the abatement of target pollutant LFX in pristine solutions, only simulated irradiation/PDS treatment achieved effective abatement of LFX in wastewater samples given the higher selectivity of SO₄•⁻. Toxicity tests were conducted with Escherichia coli (LMG2092) and Micrococcus flavus (DSM1790), demonstrating successful inhibition of the antibiotic character of polluted waters, which would contribute to preventing the development of resistant bacterial strains. Finally, a degradative pathway was suggested from the by-products and intermediates identified by LC–MS. Results demonstrate that the degradation of specific functional groups (i.e., piperazine ring) is associated with the loss of antibacterial character of the molecule.

A great deal of research has been directed towards the problem of reduction and control of volatile organic compounds (VOCs). The aim of this research is to find a process that is both efficient and inexpensive in comparison with traditional air treatment technologies.Our biofilter (one stage system, 2 m in height) is an aerobic system for waste gases containing VOCs using the degradation properties of microbial flora (assorted cultures of Bacillus, Micrococcus, Acinetobacter and yeast). In this process, polluted gas diffuses across a filter bed into which a microbial culture has previously been introduced. Peat is the medium of choice for inoculation with microorganisms because of its adsorption and absorption properties, ability to retain moisture, and buffering capacity. Furthermore, the peat utilized is spherical in shape; thus, it is possible to avoid problems related to compacting.The objective of this study was to eliminate VOCs emitted from a rotogravure process. We were able to achieve promising results from biofiltration of two types of VOCs (a mixed solvent containing isopropyl acetate and 1-nitropropane, and the solvent: 1-nitropropane). The results obtained indicate that the elimination of nitropropane and the mixed solvent in the biofilter are considered to follow zero-order kinetics with reaction rate limitation and diffusion rate limitation, respectively.

Soil microbial communities play an important role in the biodegradation of different petroleum derivates, including hydrocarbons. Also other biological factors such as enzyme and respiration activities and microbial abundance are sensitive to contamination with petroleum derivates. The aim of this study was to evaluate the response of autochthonic microbial community and biological parameters (respiration, dehydrogenase and catalase activities, total microorganisms count) on contamination with car fuels and engine oils. The surface layer (0–20 cm) of Mollic Gleysol was used for the experiment. In laboratory conditions, soil was contaminated with the following petroleum substances: car fuels (petrol, diesel) and car engine oils (new and waste—after 10,000 km). The results demonstrated that, among the investigated hydrocarbon substances, petrol addition seemed to be the most toxic for the microbial activity of the investigated soil. The toxicity of the used hydrocarbon substances to microorganisms might be summarized as follows: diesel > new oil > waste oil > petrol. Species belonging to the genera Micrococcus and Rhodococcus were noted as the major autochthonic bacteria being present in soil contaminated with new automobile oil, whereas species of the genera Bacillus sp. and Paenibacillus sp. were identified in the combination treated with waste oil.

Size-segregated aerosol samplings were carried out near the potential sources of airborne biological particles i.e. at a landfill site, an agricultural field and a road side restaurant-cluster site in winter, spring and summer seasons during 2013–2015 in New Delhi. The culturable airborne bacterial (CAB) concentrations showed significant seasonal variation from higher to moderate in spring and winter seasons and lowest during summer. Highest CAB concentrations were observed at the Okhla landfill site followed by restaurant-cluster area and agriculture site. The CAB particles showed bimodal size distribution, abundant in the size ranges of 1.1–2.1, 2.1–3.3 and 4.7–5.8 μm. However, substantial concentrations were also observed in the size bins of 0.43–0.65 and <0.43 μm, which are important for cloud condensation nuclei (CCN) activity of aerosols in addition to their adverse health effects. In spring, bacterial particles were also maximized in size ranges between 5.8 and >9.0 μm. Fine mode proportions of CAB were found to be higher in winter than other two seasons. Bacterial identification was done by 16s rDNA sequencing, and most abundant identified strains were Bacillus cereus (16%), Bacillus licheniformis (11%), Bacillus thuringiensis (9%), Micrococcus sp. (7%) and Acinetobacter sp. (9%).

The concentrations of bacterial and fungal bioaerosols were measured in a retirement home and a school dormitory from May 2012 to May 2013. In the present work, two active and passive methods were used for bioaerosol sampling. The results from the present work indicated that Bacillus spp., Micrococcus spp., and Staphylococcus spp. were the dominant bacterial genera, while the major fungal genera were Penicillium spp., Cladosporium spp., and Aspergillus spp. The results also indicated that the indoor-to-outdoor (I/O) ratios for total bacteria were 1.77 and 1.44 in the retirement home and the school dormitory, respectively; the corresponding values for total fungal spores were 1.23 and 1.08. The results suggested that in addition to outdoor sources, indoor sources also played a significant role in emitting bacterial and fungal bioaerosols in the retirement home and the school dormitory indoor.

PURPOSE: Malachite Green (MG) is used for a variety of applications but is also known to be carcinogenic and mutagenic. In this study, a novel Micrococcus sp. (strain BD15) was observed to efficiently decolorize MG. The purposes of this study were to explore the optimal conditions for decolorization and to evaluate the potential use of this strain for MG decolorization. METHODS: Optical microscope and UV–visible analyses were carried out to determine whether the decolorization was due to biosorption or biodegradation. A Plackett–Burman design was employed to investigate the effect of various parameters on decolorization, and response surface methodology was then used to explore the optimal decolorization conditions. Kinetics analysis and antimicrobial activity tests were also performed. RESULTS: The results indicated that the decolorization by the strain was mainly due to biodegradation. Concentrations of MG, urea, and yeast extract and inoculum size had significantly positive effects on MG decolorization, while concentrations of CuCl₂ and MgCl₂, and temperature had significantly negative effects. The interaction between different parameters could significantly affect decolorization, and the optimal conditions for decolorization were 1.0 g/L urea, 0.9 g/L yeast extract, 100 mg/L MG, 0.1 g/L inoculums (dry weight), and incubation at 25.2°C. Under the optimal conditions, 96.9% of MG was removed by the strain within 1 h, which represents highly efficient microbial decolorization. Moreover, the kinetic data for decolorization fit a second-order model well, and the strain showed a good MG detoxification capability. CONCLUSION: Based on the results of this study, we propose Micrococcus sp. strain BD15 as an excellent candidate strain for MG removal from wastewater.