259 research outputs found
Soybean Oil and Meal as Substrates for Lipase Production by Botryosphaeria ribis, and Soybean Oil to Enhance the Production of Botryosphaeran by Botryosphaeria rhodina
Influence of nutrients on enhancing laccase production by Botryosphaeria rhodina MAMB-05
The physiological requirements needed to enhance the production of laccases by the ascomycete Botryosphaeria
rhodina MAMB-05 in submerged cultivation were examined under non-induced and induced (veratryl alcohol, VA) conditions. Under non-induced conditions (–VA), the initial pH, C:N ratio, and inorganic N source did not influence laccase production, in contrast to Tween 80, soybean oil, and copper, which significantly increased laccase production, and proline and urea, which suppressed laccase formation. In addition, Tween 60 could serve as the sole carbon source for the production of these enzymes. Under VA-induced conditions of fungal growth, factors such as inoculum type, time-point of addition of
inducer, initial pH, C:N ratio, and type of N source, influenced the production of laccases; however, unlike the non-induced conditions, proline and urea did not act as suppressors. Each of these physiological conditions exerted different effects on biomass production. The nutritional conditions examined for B. rhodina MAMB-05 are discussed in relation to their influence on fungal growth and laccase production. [Int Microbiol 2007; 10(3):177-185
Evaluation of the Components Released by Wine Yeast Strains on Protein Haze Formation in White Wine
Cultures of 23 indigenous yeast strains (22 Saccharomyces cerevisiae and a non-Saccharomyces, Torulaspora delbrueckii), isolated from fermentation tanks at wineries in Castilla-La Mancha (Spain), and were performed under winemaking conditions using a synthetic must. Polysaccharide analysis and turbidity assays were conducted so as to observe the capacity of the released mannoproteins against protein haze formation in white wine, and 3 strains (2 Saccharomyces cerevisiae and T. delbrueckii) were chosen for further experiments. The action of a commercial b-glucanolytic enzyme preparation (Lallzyme BETA®), and a β-(1→3)-glucanase preparation from Trichoderma harzianum Rifai were evaluated to release polysaccharides from the different yeast strains’ cell walls. Protection against protein haze formation was strain dependent, and only two strains (Sc2 and Sc4) presented >50% stabilization in comparison to controls. Addition of β-glucanases did not increase the concentrations of polysaccharides in the fermentation musts; however, a significant increase of polymeric mannose (mannoproteins) was detected using an enzymatic assay following total acid hydrolysis of the soluble polysaccharides. Enzymatic treatment presented positive effects and decreased protein haze formation in white wine.
DOI http://dx.doi.org/10.17807/orbital.v8i6.86
Evaluation of Fermentative Parameters for the Production of Botryosphaeran (a(1-->3;1-->6)-β-D-glucan) and Mycelial Biomass by Botryosphaeria rhodina MAMB-05
Botryosphaeran is an exopolysaccharide (EPS) of the (1"3;1"6)-β-D-glucan type produced by the fungus Botryosphaeria rhodina MAMB-05. In attempts to enhance its extracellular production, the quantitative effects of different nitrogen sources, fermentation time, inoculum size, C/N ratio, and initial pH were evaluated on the yields of botryosphaeran. Ammonium nitrate was selected as the best nitrogen source in examining these effects using a 2³-factorial central-composite experimental design, and analysis by the response surface method. According to a factorial design, the most important variables influencing both botryosphaeran and mycelium biomass production was inoculum concentration and the time of growth. Under these conditions, optimum botryosphaeran production occurred at 88 h of growth, 0.88 g of mycelium L-1 of nutrient mediumat C/N ratio of 30, and resulted in a 5.2 g L-1 yield of EPS in the fermentation broth. For production of the mycelium biomass, the optimum condition occurred at the same time of growth and inoculum concentration; however the best C/N ratio was 75, and resulted in a yield of 33.8 g L-1 of biomass. The results also indicated that the maximal mycelial growth is not associated to the yields of botryosphaeran production by Botryosphaeria rhodina MAMB-05.
DOI:Â http://dx.doi.org/10.17807/orbital.v7i1.63
Sulfonated (1→6)-β-D-Glucan (Lasiodiplodan): Preparation, Characterization and Bioactive Properties
U radu su proizvedeni sulfonirani derivati β-D-glukana iz gljive Lasiodiplodia theobromae MMPI, nazvani lasiodiplodan (LAS-S), s različitim stupnjevima supstitucije (1,61; 1,42; 1,02 i 0,15), te su okarakterizirani pomoću FTIR spektroskopije i skenirajuće elektronske mikroskopije (SEM). Ispitani su toplinska svojstva, topljivost, te antimikrobni, antioksidacijski i citotoksički učinak derivata. Uspješnost sulfonacije provjerena je FTIR analizom, pri čemu su dobivene specifične vrpce na 1250 cm-1 (S=O, jaki signal za asimetričnu vibraciju rastezanja dvostruke veze) i 810 cm-1 (C-O-S, signal za simetričnu vibraciju povezan s prisustvom C-O-SO3 skupine) u sulfoniranim uzorcima. SEM analizom je potvrđeno da sulfonacija pospješuje morfološke promjene na površini biopolimera, uz pojavu heterogenih fibrilarnih struktura na površini nakon kemijske modifikacije. Sulfonirani je lasiodiplodan imao veliku toplinsku stabilnost, a zbog oksidacije pri gotovo 460 °C opažen je gubitak mase. Sulfonacijom je povećana topljivost lasiodiplodana i njegova antimikrobna aktivnost, osobito spram kvasca Candida albicans i bakterije Salmonella enterica Typhimurium. Prirodni je lasiodiplodan bolje uklanjao ione OH˙, dok je sulfonirani bolje uklanjao ione željeza (FRAP potencijal). Ni prirodni ni sulfonirani lasiodiplodan nisu imali citotoksični učinak na divlje tipove i mutante kvasca Saccharomyces cerevisiae. Uzorci s većim stupnjem supstitucije (1,42 i 1,61) imali su slabije svojstvo indukcije oksidacijskog stresa.Sulfonated derivatives of lasiodiplodan (LAS-S) with different degrees of substitution (1.61, 1.42, 1.02 and 0.15) were obtained and characterized by Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and thermal and solubility analyses. Antimicrobial, antioxidant and cytotoxic potential were also assessed. The sulfonation was confirmed by FTIR analysis with specific bands at 1250 cm–1 (S=O, strong asymmetrical stretching vibration) and at 810 cm–1 (C-O-S, symmetrical vibration associated with the C-O-SO3 group) in the sulfonated samples. SEM demonstrated that sulfonation promoted morphological changes on the surface of the biopolymer with heterogeneous fibrillary structures appearing along the surface following chemical modification. LAS-S showed high thermal stability, with mass loss due to oxidation at temperatures close to 460 °C. Sulfonation increased the solubility of LAS, and in addition, increased the antimicrobial activity, especially against Candida albicans (fungicidal) and Salmonella enterica Typhimurium (bacteriostatic). Native lasiodiplodan (LAS-N) showed higher OH˙ removal capacity, while LAS-S had higher ferric ion reducing antioxidant power (FRAP) potential. LAS-N and LAS-S did not demonstrate lethal cytotoxicity against wild and mutant strains of Saccharomyces cerevisiae. Samples with higher degree of substitution (1.42 and 1.61) showed lower potential to induce oxidative stress
The Unique Origin of Colors of Armchair Carbon Nanotubes
The colors of suspended metallic colloidal particles are determined by their
size-dependent plasma resonance, while those of semiconducting colloidal
particles are determined by their size-dependent band gap. Here, we present a
novel case for armchair carbon nanotubes, suspended in aqueous medium, for
which the color depends on their size-dependent excitonic resonance, even
though the individual particles are metallic. We observe distinct colors of a
series of armchair-enriched nanotube suspensions, highlighting the unique
coloration mechanism of these one-dimensional metals.Comment: 4 pages, 3 figure
Effect of Particle Size on Droplet Infiltration into Hydrophobic Porous Media As a Model of Water Repellent Soil
The wettability of soil is of great importance for plants and soil biota, and in determining the risk for preferential flow, surface runoff, flooding,and soil erosion. The molarity of ethanol droplet (MED) test is widely used for quantifying the severity of water repellency in soils that show reduced wettability and is assumed to be independent of soil particle size. The minimum ethanol concentration at which droplet penetration occurs within a short time (≤10 s) provides an estimate of the initial advancing contact angle at which spontaneous wetting is expected. In this study, we test the assumption of particle size independence using a simple model of soil, represented by layers of small (0.2–2 mm) diameter beads that predict the effect of changing bead radius in the top layer on capillary driven imbibition. Experimental results using a three-layer bead system show broad agreement with the model and demonstrate a dependence of the MED test on particle size. The results show that the critical initial advancing contact angle for penetration can be considerably less than 90° and varies with particle size, demonstrating that a key assumption currently used in the MED testing of soil is not necessarily valid
Suspected Lynch syndrome associated MSH6 variants: A functional assay to determine their pathogenicity
Lynch syndrome (LS) is a hereditary cancer predisposition caused by inactivating mutations in DNA mismatch repair (MMR) genes. Mutations in the MSH6 DNA MMR gene account for approximately 18% of LS cases. Many LS-associated sequence variants are nonsense and frameshift mutations that clearly abrogate MMR activity. However, missense mutations whose functional implications are unclear are also frequently seen in suspected-LS patients. To conclusively diagnose LS and enroll patients in appropriate surveillance programs to reduce morbidity as well as mortality, the functional consequences of these variants of uncertain clinical significance (VUS) must be defined. We present an oligonucleotide-directed mutagenesis screen for the identification of pathogenic MSH6 VUS. In the screen, the MSH6 variant of interest is introduced into mouse embryonic stem cells by site-directed mutagenesis. Subsequent selection for MMR-deficient cells using the DNA damaging agent 6-thioguanine (6TG) allows the identification of MMR abrogating VUS because solely MMR-deficient cells survive 6TG exposure. We demonstrate the efficacy of the genetic screen, investigate the phenotype of 26 MSH6 VUS and compare our screening results to clinical data from suspected-LS patients carrying these variant alleles
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