Biosorption and Biovolatilization of Arsenic by Heat-Resistant Fungi (5 pp)

Goal, Scope and Background

The aim of this work is to show the ability of several fungal species, isolated from arsenic polluted soils, to biosorb and volatilize arsenic from a liquid medium under laboratory conditions. Mechanisms of biosorption and biovolatilization play an important role in the biogeochemical cycle of arsenic in the environment. The quantification of production of volatile arsenicals is discussed in this article.

Methods

Heat-resistant filamentous fungi Neosartorya fischeri, Talaromyces wortmannii, T. flavus, Eupenicillium cinnamopurpureum, originally isolated from sediments highly contaminated with arsenic (more than 1403 mg.l-1 of arsenic), and the non-heat-resistant fungus Aspergillus niger were cultivated in 40 mL liquid Sabouraud medium (SAB) enriched by 0.05, 0.25, 1.0 or 2.5 mg of inorganic arsenic (H3AsO4). After 30-day and 90-day cultivation under laboratory conditions, the total arsenic content was determined in mycelium and SAB medium using the HG AAS analytical method. Production of volatile arsenic derivates by the Neosartorya fischeri strain was also determined directly by hourly sorption using the sorbent Anasorb CSC (USA).

Results

Filamentous fungi volatilized 0.025–0.321 mg of arsenic from the cultivation system, on average, depending on arsenic concentrations and fungal species. The loss of arsenic was calculated indirectly by determining the sum of arsenic content in the mycelium and culture medium. The amount of arsenic captured on sorption material was 35.7 ng of arsenic (22nd day of cultivation) and 56.4 ng of arsenic (29th day of cultivation) after one hour's sorption. Biosorption of arsenic by two types of fungal biomass was also discussed, and the biosorption capacity for arsenic of pelletized and compact biomass of Neosartorya fischeri was on average 0.388 mg and 0.783 mg of arsenic, respectively.

Discussion

The biosorption and amount of volatilized arsenic for each fungal species was evaluated and the effect of initial pH on the biovolatilization of arsenic was discussed.

Conclusions

The most effective biovolatilization of arsenic was observed in the heat-resistant Neosartorya fischeri strain, while biotransformation of arsenic into volatile derivates was approximately two times lower for the non-heat-resistant Aspergillus niger strain. Biovolatilization of arsenic by Talaromyces wortmannii, T. flavus, Eupenicillium cinnamopurpureum was negligible. Results from biosorption experiments indicate that nearly all of an uptaken arsenic by Neosartorya fischeri was transformed into volatile derivates.

Recommendations and Perspective

. Biovolatilization and biosorption have a great potential for bioremediation of contaminated localities. However, results showed that not all fungal species are effective in the removal of arsenic. Thus, more work in this research area is needed.

     

Triclosan—the forgotten priority substance?

Introduction  

Triclosan (TCS) is a multi-purpose biocide. Its wide use in personal care products (PCPs) fosters its dispersal in the aquatic environment. Despite enhanced awareness of both scientists and the public in the last decade with regard to fate and effects, TCS received little attention regarding its prioritisation as a candidate river basin-specific pollutant or even priority substance, due to scarce monitoring data.     

The effect of deoxynivalenol on the secretion activity, proliferation and apoptosis of porcine ovarian granulosa cells in vitro

The aim of this in vitro study was to examine the secretion activity, markers of proliferation and apoptosis in porcine ovarian granulosa cells (GCs) after deoxynivalenol (DON) addition. Ovarian granulosa cells were incubated with DON for 24h: 10, 100 and 1000 ng/mL, while the control group received no DON. The secretion of insulin-like growth factor I (IGF-I) and progesterone was determined by radioimmunoassay (RIA) and expression of cyclin B1, PCNA and caspase-3 by immunocytochemistry. IGF-I release by GCs was inhibited by DON, while progesterone release and the expression of cyclin B1 was stimulated by DON (at 1000 ng/mL but not at 10 and 100 ng/mL). PCNA expression was stimulated by DON (at 100 and 1000 ng/mL but not at 10 ng/mL). Caspase-3 expression was not influenced by DON treatment (at all doses). In conclusion, our results indicate, (1) a direct effect of DON on secretion of growth factor IGF-I and steroid hormone progesterone, (2) expression of markers of proliferation (cyclin B1 and PCNA) but not on the (3) expression of marker of apoptosis (caspase-3) in porcine ovarian granulosa cells. This in vitro study suggests the dose-dependent association of DON on porcine ovarian functions.     

Variation in sperm morphometry and sperm competition among barn swallow (Hirundo rustica) populations

Spermatozoa vary greatly in size and shape among species across the animal kingdom. Postcopulatory sexual selection is thought to be the major evolutionary force driving this diversity. In contrast, less is known about how sperm size varies among populations of the same species. Here, we investigate geographic variation in sperm size in barn swallows Hirundo rustica, a socially monogamous passerine with a wide Holarctic breeding distribution. We included samples from seven populations and three subspecies: five populations of ssp. rustica in Europe (Czech, Italy, Norway, Spain, and Ukraine), one population of ssp. transitiva in Israel, and one population of ssp. erythrogaster in Canada. All sperm traits (head length, midpiece length, tail length, and total length) varied significantly among populations. The variation among the European rustica populations was much lower than the differences among subspecies, indicating that sperm traits reflect phylogenetic distance. We also performed a test of the relationship between the coefficient of between-male variation in total sperm length and extrapair paternity levels across different populations within a species. Recent studies have found a strong negative relationship between sperm size variation and extrapair paternity among species. Here, we show a similar negative relationship among six barn swallow populations, which suggests that the variance in male sperm length in a population is shaped by the strength of stabilizing postcopulatory sexual selection.     

Degradation of juvenile hormone analog by soil microbial isolates

Juvenoids are efficient pesticides with relatively low toxicity to humans. However, few studies have evaluated the effect of degradation by soil microorganisms on their toxicity. The effects of bacterial, fungal and yeast isolates on aerobic decomposition of ethyl N-[2-[4-(2,2-ethylenedioxy-1-cyclohexylmethyl)phenoxy]ethyl] carbamate during eight weeks were determined. The effect of different concentration of glucose on their degradation activity is also analyzed.     

Application of large volume injection GC-MS to analysis of organic compounds in the extracts and leachates of municipal solid waste incineration fly ash

Organic solvent and water extracts of fly ash from a Milan (Italy) municipal solid waste incinerator (MSWI) were analyzed by large volume injection-gas chromatography-mass spectrometry (LVI-GC-MS) with programmable temperature vaporizer (PTV). Using injection volumes of 10-100 microl, typically over a hundred compounds were detected in organic solvent extracts and ca. 35% of them could be tentatively identified from their electron impact ionization mass spectra. A protocol for the determination of the maximum amount of a potential environmental pollutant available for leaching (availability test) was developed for four selected target compounds: pentachlorobenzene (PeCB), hexachlorobenzene (HxCB), o-terphenyl (o-TPH) and m-terphenyl (m-TPH). Key parameters, extraction time and liquid-to-solid ratio (L/S), were studied in more detail. Recoveries of PeCB, HxCB and o-TPH spiked into the fly ash samples at two concentration levels ranged from 38% to 53% for freshly spiked and from 14% to 40% for 40-day aged fly ash. Recoveries of m-TPH were 8% to 11% from freshly spiked and less than 3% from aged spiked fly ash. The native amounts in Milan MSWI fly ash, determined in an interlaboratory exercise using the developed protocol, were 31 ng/g PeCB, 34 ng/g HxCB, 72 ng/g o-TPH and 4.4 ng/g m-TPH. A separate methodology was developed for the determination of compounds extracted from fly ash by water (leaching test). Following 8-h sonication at L/S 20, the leached amounts of PeCB, HxCB and o-TPH were 1.1, 3.1 and 6.0 ng/g fly ash, respectively.     

Detection of Listeria monocytogenes in ready-to-eat food by Step One real-time polymerase chain reaction

The aim of this study was to follow contamination of ready-to-eat food with Listeria monocytogenes by using the Step One real time polymerase chain reaction (PCR). We used the PrepSEQ Rapid Spin Sample Preparation Kit for isolation of DNA and MicroSEQ? Listeria monocytogenes Detection Kit for the real-time PCR performance. In 30 samples of ready-to-eat milk and meat products without incubation we detected strains of Listeria monocytogenes in five samples (swabs). Internal positive control (IPC) was positive in all samples. Our results indicated that the real-time PCR assay developed in this study could sensitively detect Listeria monocytogenes in ready-to-eat food without incubation.