Figure 6 HR-XRD analysis The Debye-Scherrer equation (D = 0 89λ/

Figure 6 HR-XRD analysis. The Debye-Scherrer equation (D = 0.89λ/Wcosθ) was employed to estimate the particle diameter from the (111) peak, and the estimated diameter was approximately 16.6 nm. The definition of each term in the equation is as follows: λ is the wavelength of CuKα radiation (0.1541 nm), W is the full-width at half-maximum of the (111) peak, θ is the diffraction angle, and D is the particle diameter. Catalytic activity Selleck HIF inhibitor toward 4-nitrophenol reduction The catalytic activity of green-synthesized AuNPs has been evaluated by other researchers [19–24]. The biological entities used in these studies

were cyclodextrins and plant extracts (a glucan of an edible mushroom (Pleurotus florida), Trigonella foenum-graecum, ayurvedic arishtams, Anacardium occidentale, and Gnidia glauca). The merit of our method over these reports lies in its

energy-saving process, in which no input of external energy is used for the green synthesis of the catechin-AuNPs; in contrast, the other methods used elevated temperatures for the reactions. To evaluate the catalytic activity of the catechin-AuNPs, the reduction reaction of 4-NP to 4-AP in the presence of NaBH4 was studied. When NaBH4 was added to 4-NP, the color of the solution became yellow, which resulted in a peak at 400 nm in the UV-visible spectrum because of the formation of the 4-nitrophenolate anion. The reaction did not proceed any further in the C646 absence of the catechin-AuNP catalyst. Upon the addition of catechin-AuNPs, the appearance of 4-AP was monitored by the emergence of a peak at 300 nm with a concomitant decrease in the intensity of the peak at 400 nm (Figure 7A). The decreased intensity of the peak at 400 nm and the appearance of the peak at 300 nm were quantitatively monitored by UV-visible Methocarbamol spectrophotometry. The approximate time required for the completion of the reaction was 30 min. Figure 7 4-NP reduction by NaBH 4 in the presence of catechin-AuNPs catalyst. (A) UV-visible spectra and (B) a plot of ln(C t /C 0) as a function of time (min). The relationship between ln(C t /C 0) and time (min) revealed a linear correlation (y = −0.091x + 0.071,

r 2 = 0.981), where C 0 and C t are the 4-NP concentration at time 0 and time t, respectively (Figure 7B) [21]. The ratio of absorbance, A t /A 0, could be substituted for the ratio of concentration, C t /C 0 (i.e., C t /C 0 = A t /A 0) because the concentration of 4-NP is proportional to its absorbance [21]. On the basis of these results, we determined that the shell did not affect the catalytic activity of the catechin-AuNPs. Conclusions Catechin, which is a potent antioxidant, has been successfully utilized as a green reducing agent for the synthesis of AuNPs. No external energy was necessary during the 1 h reaction, which was simple, fast, energy-saving, and eco-friendly. Together with spherically shaped AuNPs, anisotropic AuNPs with diverse shapes were also observed.

mycoides SC Vet Microbiol 2004, 98:229–234 CrossRefPubMed 3 Gon

mycoides SC. Vet Microbiol 2004, 98:229–234.CrossRefPubMed 3. Gonçalves R, Regalla J, Nicolet J, Frey J, Nicholas R, Bashiruddin J, De Santis P, Gonçalves AP: Antigen heterogeneity among Mycoplasma mycoides subsp. mycoides SC isolates: discrimination of major surface proteins. Vet Microbiol 1998, 63:13–28.CrossRefPubMed Selleckchem PXD101 4. Niang M, Diallo M, Cisse O, Kone M, Doucoure M, Roth JA, Balcer-Rodrigues V, Dedieu L: Pulmonary and serum antibody responses elicited in zebu cattle experimentally infected with Mycoplasma mycoides subsp. mycoides SC by contact exposure.

Vet Res 2006, 37:733–744.CrossRefPubMed 5. Westberg J, Persson A, Holmberg A, Goesmann A, Lundeberg J, Johansson KE, Pettersson B, Uhlen M: The genome sequence of

Mycoplasma mycoides subsp. mycoides SC type strain PG1 T , the causative agent of contagious bovine pleuropneumonia (CBPP). Genome Res 2004, 14:221–227.CrossRefPubMed 6. Masiga WN, Roberts DH, Kakoma I, Rurangirwa FR: Passive immunity to contagious bovine pleuropneumonia. Res Vet Sci 1975, 19:330–332.PubMed 7. Masiga WN, Windsor RS: Immunity to contagious bovine pleuropneumonia. Vet Rec 1975, 97:350–351.CrossRefPubMed 8. Dedieu L, Balcer-Rodrigues learn more V, Cisse O, Diallo M, Niang M: Characterisation of the lymph node immune response following Mycoplasma mycoides subsp. mycoides SC infection in cattle. Vet Res 2006, 37:579–591.CrossRefPubMed 9. Dedieu L, Balcer-Rodrigues V, Yaya A, Hamadou B, Cisse

O, Diallo M, Niang M: Gamma interferon-producing CD4 T-cells correlate with resistance to Mycoplasma mycoides subsp. mycoides S.C. infection in cattle. Vet Immunol Immunopathol 2005, 107:217–233.CrossRefPubMed 10. Totté P, Rodrigues V, Yaya A, Hamadou B, Cisse O, Diallo M, Niang M, Thiaucourt F, Dedieu L: Analysis of cellular responses to Mycoplasma mycoides subsp. mycoides small colony biotype associated with control of contagious bovine pleuropneumonia. Vet Res 2008, 39:8.CrossRefPubMed Neratinib purchase 11. Dedieu-Engelmann L: Contagious bovine pleuropneumonia: a rationale for the development of a mucosal sub-unit vaccine. Comp Immunol Microbiol Infect Dis 2008, 31:227–238.CrossRefPubMed 12. Smith GP: Filamentous fusion phage: novel expression vectors that display cloned antigens on the virion surface. Science 1985, 228:1315–1317.CrossRefPubMed 13. Wang LF, Yu M: Epitope identification and discovery using phage display libraries: applications in vaccine development and diagnostics. Curr Drug Targets 2004, 5:1–15.CrossRefPubMed 14. Wang LF, du Plessis DH, White JR, Hyatt AD, Eaton BT: Use of a gene-targeted phage display random epitope library to map an antigenic determinant on the bluetongue virus outer capsid protein VP5. J Immunol Methods 1995, 178:1–12.CrossRefPubMed 15. Fehrsen J, du Plessis DH: Cross-reactive epitope mimics in a fragmented-genome phage display library derived from the rickettsia, Cowdria ruminantium.

In the present study, despite its selectivity, plate cultivation

In the present study, despite its selectivity, plate cultivation was partly successful in reflecting increased fungal diversity and/or detecting major indicator fungi arising from building material sources in settled dust samples. This was not, however, consistent Neratinib mw across all samples, as the masking effect of certain

species occurring in very high concentrations was considerable. ERMI is an index derived from a set of qPCR assays used to describe the indoor fungal burden [20]. Here, the ERMI values were below 5, i.e. relatively low compared to US homes. Vesper et al. reported ERMI values greater than 5 for the highest quartile of randomly selected US homes, whereas over 75% of homes with asthmatic children were above this value [54]. However, no similar data are available in Finland. In the present study, the ERMI index was observed to reflect the overall level of diversity. In our sample material, the group 1 members A. pullulans and Eurotium spp. occurred in significant concentrations in all studied dust samples and in similar concentrations in the index and reference buildings. This suggests that the placement of these species in the indicator group may not be appropriate. Conclusions The present study is the first to assess the effect of water damage and

its remediation on indoor mycobiota using universal culture-independent community characterization see more methods, and also the first study to compare nucITS sequencing results with an extensive panel of mold specific qPCR assays. Observations were made from a small number of buildings, and thus the findings are descriptive and need to be studied further with larger data sets. In the studied buildings, we found RANTES indications of elevated fungal diversity, as well as the presence of fungi attributable to building growth to be associated with water damage. The community variation between buildings was significant,

and calls for the analysis of larger data sets in order to understand the dynamics of microbial communities between building structures, surfaces and dust. Our results demonstrate that culture-based methods used to characterize indoor mycobiota provide an underestimate of the total diversity, and that many unknown or unsequenced fungal species are present in dust. Despite this, the majority of abundant phylotypes in nucITS clone libraries were affiliated with previously recognized indoor taxa, indicating that culture-dependent and independent methods agree on the dominant indoor taxa. Clone library sequencing was seen as an effective means to characterize indoor communities, and proves extremely useful when attempting to answer research questions on ‘real’ fungal diversity in a given environment.