214 results on '"enzyme treatment"'
Search Results
202. Processing of Hemp Fibre Using Enzyme/Fungal Treatment for Composites
- Abstract
Hemp fibres compete very well with glass fibres in terms of their specific strength and stiffness and so can replace glass fibres as reinforcement in composites. Combining them with thermoplastics results in potentially cheap recyclable composite materials. The adhesion between the hemp fibre and thermoplastics such as polypropylene is a major factor in the mechanical properties of the composite. Interfacial bonding can be improved by modifications to the fibres, the matrix or both the fibres and the matrix. The aim of this thesis was to investigate low cost and efficient fibre treatment methods with low environmental impact such as bag retting and white rot fungi, and chelator/enzyme treatments which could be applied to hemp fibre in order to create better bonding fibre for potentially recyclable composite materials. Bag retting was carried out by keeping fresh green hemp fibres in a sealed plastic bag for 1 to 2 weeks to allow natural retting to occur under sealed conditions. For white rot fungi treatments, the dried non-retted hemp fibres were gamma irradiated, and then inoculated with white rot fungi for 2 weeks. Chelator/enzyme treatment was achieved by immersing the fresh green non-retted hemp fibres in solutions consisting of either EDTMP.Na5 (ethylene diamine tetra (methylene phosphonic acid pentasodium salt) or pectinase (P2401) and laccase (53739) for 6 hours. Several characterization techniques, namely wet chemical analysis, Fourier-transform infrared (FT-IR), scanning electron microscopy (SEM), fibre density testing, X-ray diffraction (XRD), differential thermal analysis (DTA) and thermogravimetric analysis (TGA), zeta potential and single fibre tensile testing were used to assess the effect of treatment on hemp fibres. Wet chemical analysis and FT-IR, were used to measure the chemical compounds present in untreated and treated hemp fibres and showed all treatments removed non-cellulosic compounds from hemp fibre. The separation of untreated and treated
- Published
- 2009
203. Processing of Hemp Fibre Using Enzyme/Fungal Treatment for Composites
- Abstract
Hemp fibres compete very well with glass fibres in terms of their specific strength and stiffness and so can replace glass fibres as reinforcement in composites. Combining them with thermoplastics results in potentially cheap recyclable composite materials. The adhesion between the hemp fibre and thermoplastics such as polypropylene is a major factor in the mechanical properties of the composite. Interfacial bonding can be improved by modifications to the fibres, the matrix or both the fibres and the matrix. The aim of this thesis was to investigate low cost and efficient fibre treatment methods with low environmental impact such as bag retting and white rot fungi, and chelator/enzyme treatments which could be applied to hemp fibre in order to create better bonding fibre for potentially recyclable composite materials. Bag retting was carried out by keeping fresh green hemp fibres in a sealed plastic bag for 1 to 2 weeks to allow natural retting to occur under sealed conditions. For white rot fungi treatments, the dried non-retted hemp fibres were gamma irradiated, and then inoculated with white rot fungi for 2 weeks. Chelator/enzyme treatment was achieved by immersing the fresh green non-retted hemp fibres in solutions consisting of either EDTMP.Na5 (ethylene diamine tetra (methylene phosphonic acid pentasodium salt) or pectinase (P2401) and laccase (53739) for 6 hours. Several characterization techniques, namely wet chemical analysis, Fourier-transform infrared (FT-IR), scanning electron microscopy (SEM), fibre density testing, X-ray diffraction (XRD), differential thermal analysis (DTA) and thermogravimetric analysis (TGA), zeta potential and single fibre tensile testing were used to assess the effect of treatment on hemp fibres. Wet chemical analysis and FT-IR, were used to measure the chemical compounds present in untreated and treated hemp fibres and showed all treatments removed non-cellulosic compounds from hemp fibre. The separation of untreated and treated
- Published
- 2009
204. Enzymatic modification of wool with tyrosinase and peroxidase
- Author
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G. Freddi, A. Miettinen-Oinonen, R. Lantto, A Lappalainen, M-L. Niku-Paavola, J. Buchert, and E. Heine
- Subjects
Polymers and Plastics ,genetic structures ,Materials Science (miscellaneous) ,Tyrosinase ,chemical and pharmacologic phenomena ,peroxidase ,proteinaceous fibre ,tyrosinase ,Industrial and Manufacturing Engineering ,Hydrolysis ,Wool fibre ,Tyrosine ,chemistry.chemical_classification ,biology ,Chemistry ,technology, industry, and agriculture ,eye diseases ,enzyme treatment ,Enzyme ,Biochemistry ,Wool ,biology.protein ,Surface modification ,General Agricultural and Biological Sciences ,tyrosine ,Peroxidase ,cross-linking - Abstract
The capabilities of tyrosinase and peroxidase to activate tyrosine residues of wool fibres and to catalyze crosslink formation between peptides derived from a wool protein hydrolyzate were investigated. Peroxidases were able to catalyse oxidation of wool fibres corresponding to 35–40% of the tyrosine residues located on the wool surface or 2% of the tyrosine residues in the wool fibre. Similar fibre surface modification was detected with tyrosinase and a fungal peroxidase using x-ray photoelectron spectroscopy. Tyrosinase did not show detectable activation of fibres measured as oxygen consumption. Tyrosinase was, however, able to crosslink peptides of 3–10 kDa derived from enzymatically hydrolysed wool fibres. Surprisingly, no crosslinking was detected with peroxidase.
- Published
- 2005
- Full Text
- View/download PDF
205. Influence of depectinization in the ultrafiltration of West Indian cherry (Malpighia glabra L.) and pineapple (Ananas comosus (L.) Meer) juices
- Author
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Sueli T. D. Barrosi, Elisabete Scolin Mendes, and Leila Peres
- Subjects
food.ingredient ,Chromatography ,Pectin ,biology ,Chemistry ,Ultrafiltration ,biology.organism_classification ,Malpighia glabra ,enzyme treatment ,food ,Membrane ,Cherry juice ,ceramic tubular ,Hollow fiber membrane ,comic_books ,clarification ,polysulfone hollow fiber ,Molecular weight cut-off ,Ananas ,comic_books.series ,membrane ,Food Science ,Biotechnology - Abstract
West Indian cherry (Malpighia glabra L.) and pineapple (Ananas comosus (L.) Meer)juice clarification by cross-flow UF, using polysulphone hollow fiber and ceramic tubular membranes with, respectively, nominal molecular weight cut off values of 100kDaltons and average pore diameters of 0.01mm, were studied. The influence of enzymatic treatment using enzyme concentrations of 20, 100 and 300mg/L, a time of 90min and a temperature of 40oC for depectinization was verified. The juices were then clarified in a laboratory scale filtration unit, with an effective filtration area of 0.12m2 for the polysulphone hollow fiber membrane and of 0.005m2 for the ceramic tubular membranes. The influence of enzymatic treatment on viscosity, turbidity and total pectin of the juice, before ultrafiltration, is reported. Membrane performance was evaluated in terms of flow rate and clarity of the permeate. The permeate flow rate of depectinized pineapple juice was higher (30 - 60%) for both membranes. Depectinized West Indian cherry juice presented a lower permeate flow rate for the polysulphone hollow fiber membrane. The increase in permeate flow rate, with the use of the 300mg/L and 100mg/L enzyme concentration was not significant, so it is economically advantageous to ultrafilter depectinized juice, treated with an enzyme concentration of 20mg/L.
- Published
- 2004
206. Influence of depectinization in the ultrafiltration of West Indian cherry (Malpighia glabra L.) and pineapple (Ananas comosus (L.) Meer) juices
- Author
-
Barrosi, Sueli T. D., Mendes, Elisabete S, and Peres, Leila
- Subjects
enzyme treatment ,ceramic tubular ,polisulfona fibra oca ,clarification ,clarificação ,polysulfone hollow fiber ,tratamento enzimático ,membrana ,membrane ,cerâmica tubular - Abstract
West Indian cherry (Malpighia glabra L.) and pineapple (Ananas comosus (L.) Meer)juice clarification by cross-flow UF, using polysulphone hollow fiber and ceramic tubular membranes with, respectively, nominal molecular weight cut off values of 100kDaltons and average pore diameters of 0.01mm, were studied. The influence of enzymatic treatment using enzyme concentrations of 20, 100 and 300mg/L, a time of 90min and a temperature of 40ºC for depectinization was verified. The juices were then clarified in a laboratory scale filtration unit, with an effective filtration area of 0.12m² for the polysulphone hollow fiber membrane and of 0.005m² for the ceramic tubular membranes. The influence of enzymatic treatment on viscosity, turbidity and total pectin of the juice, before ultrafiltration, is reported. Membrane performance was evaluated in terms of flow rate and clarity of the permeate. The permeate flow rate of depectinized pineapple juice was higher (30 - 60%) for both membranes. Depectinized West Indian cherry juice presented a lower permeate flow rate for the polysulphone hollow fiber membrane. The increase in permeate flow rate, with the use of the 300mg/L and 100mg/L enzyme concentration was not significant, so it is economically advantageous to ultrafilter depectinized juice, treated with an enzyme concentration of 20mg/L. Foi estudada a clarificação através da ultrafiltração por flow rateo cruzado, dos sucos de acerola (Malpighia glabra L.) e Abacaxi (Ananas comosus (L.) Meer), usando membranas de polisulfona fibra oca e tubular cerâmica com peso molecular de corte de 100kDaltons e diâmetro médio de poro de 0,01mm, respectivamente. A influência do tratamento dos sucos, com concentrações de enzima de 20, 100 e 300mg/L, tempo de tratamento de 90min a temperatura de 40ºC, foi verificada, e então os mesmos foram clarificados numa unidade de ultrafiltração com uma área efetiva de 0,12m² para a membrana de polisulfona e de 0,005m² para membrana cerâmica. A influência do tratamento enzimático foi avaliada em termos da viscosidade, turbidez e pectina total do suco, antes da ultrafiltração. Os desempenhos das membranas foram avaliados em termos de flow rate permeado e claridade do permeado. O flow rate permeado do suco de abacaxi tratado foi mais alto (30 - 60%) para ambas as membranas do que para o suco natural. O suco de West Indian cherry despectinizado apresentou flow rate permeado menor para a membrana de polisulfona. O aumento de flow rate, observado com 300mg/L e 100mg/L de enzima não foi significante, concluindo-se que é vantajoso o tratamento com uma concentração de enzima de 20mg/L.
- Published
- 2004
207. Isolation of Individual Egg Cells and Zygotes in Alstroemeria Followed by Manual Selection with a Microcapillary-connected Micropump
- Author
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1000050301875, HOSHINO, Yoichiro, MURATA, Naho, SHINODA, Koichi, 1000050301875, HOSHINO, Yoichiro, MURATA, Naho, and SHINODA, Koichi
- Abstract
Aims: To develop a procedure for isolating living egg cells and zygotes from Alstroemeria ovules. Scope: We attempted to isolate egg cells and zygotes from the ovules of Alstroemeria aurea. The ovules were histologically observed using a clearing procedure which revealed the localization and sizes of the embryo sacs and egg apparatus within the ovules. For the isolation of egg cells, ovules were cut into sections with a surgical blade and treated with an enzyme solution. Subsequently, these ovule sections were dissected using a glass needle under an inverted microscope. Egg cells successfully isolated by this procedure were collected using microcapillaries connected to a micropump. For zygote isolation, ovules were excised from ovaries 24 hours after self-pollination. By treating excised ovules with an enzyme solution and subsequently dissecting them using a glass needle, zygotes were successfully isolated from the ovules and collected with a microcapillary. The isolated zygotes were associated with pollen tubes and one of the synergids. Egg cells and zygotes were viable for up to 2 h following isolation, as determined by fluorescein diacetate staining. Conclusions: The procedures for isolating egg cells and zygotes in Alstroemeria were established, and each egg cell and zygote was captured with a microcapillary.
- Published
- 2006
208. Activation of a Plasmalemma K+ Efflux/H+ Influx Mechanism in Tobacco by Incompatible Bacteria or Pectate Lyase
- Author
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Atkinson, M. M., Backer, C. J., Huang, J. S., Collmer, A., Knopp, J. A., Bliss, F. A., editor, Civerolo, E. L., editor, Collmer, A., editor, Davis, R. E., editor, and Gillaspie, A. G., editor
- Published
- 1987
- Full Text
- View/download PDF
209. [Bacterial prostatitis and prostatic fibrosis: modern view on the treatment and prophylaxis].
- Author
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Zaitsev AV, Pushkar DY, Khodyreva LA, and Dudareva AA
- Subjects
- Bacterial Infections drug therapy, Bacterial Infections pathology, Fibrosis, Humans, Hyaluronoglucosaminidase therapeutic use, Male, Polymers therapeutic use, Prostatic Diseases drug therapy, Prostatic Diseases pathology, Prostatitis drug therapy, Prostatitis pathology, Bacterial Infections microbiology, Prostatic Diseases microbiology, Prostatitis microbiology
- Abstract
Treatments of chronic bacterial prostatitis (CP) remain difficult problem. Bacterial prostatitis is a disease entity diagnosed clinically and by evidence of inflammation and infection localized to the prostate. Risk factors for UTI in men include urological interventions, such as transrectal prostate biopsy. Ensuing infections after prostate biopsy, such as UTI and bacterial prostatitis, are increasing due to increasing rates of fluoroquinolone resistance. The increasing global antibiotic resistance also significantly affects management of UTI in men, and therefore calls for alternative strategies. Prostatic inflammation has been suggested to contribute to the etiology of lower urinary tract symptoms (LUTS) by inducing fibrosis. Several studies have shown that prostatic fibrosis is strongly associated with impaired urethral function and LUTS severity. Fibrosis resulting from excessive deposition of collagen is traditionally recognized as a progressive irreversible condition and an end stage of inflammatory diseases; however, there is compelling evidence in both animal and human studies to support that the development of fibrosis could potentially be a reversible process. Prostate inflammation may induce fibrotic changes in periurethral prostatic tissues, promote urethral stiffness and LUTS. Patients experiencing CP and prostate-related LUTS could benefit from anti-inflammatory therapies, especially used in combination with the currently prescribed enzyme treatment with Longidase. Treatment results showed that longidase is highly effective in bacterial and abacterial CP. Longidase addition to standard therapeutic methods significantly reduced the disease symptoms and regression of inflammatory-proliferative alterations in the prostate.
- Published
- 2016
210. Emerging drugs for celiac disease.
- Author
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Freeman HJ
- Subjects
- Administration, Oral, Celiac Disease diet therapy, Celiac Disease physiopathology, Drug Design, Glutens adverse effects, Humans, Patient Compliance, Peptide Hydrolases administration & dosage, Celiac Disease drug therapy, Diet, Gluten-Free, Peptide Hydrolases therapeutic use
- Abstract
Introduction: Celiac disease is an immune-mediated gluten-dependent disorder, primarily affecting the small intestine in genetically predisposed individuals. The disorder has a very heterogeneous clinical and histopathological spectrum. Current treatment with a gluten-free diet is very effective, but the diet is difficult to maintain and remains costly., Areas Covered: Alternatives to the gluten-free diet have been proposed to either replace this current treatment, or at least, to supplement use of the gluten-free diet. Studies in the published English language literature relevant to this review were examined for this report., Expert Opinion: Most recent published double-blind, placebo-controlled clinical trials have focused on an orally administered recombinant glutenase (ALV003) showing significant but limited benefit to celiac disease patients already compliant with a gluten-free diet. Other studies have addressed other immune mechanisms that may play a role in its pathogenesis and have not been so positive. Added investigations, particularly over the long-term, in other larger and more heterogeneous populations are needed.
- Published
- 2015
- Full Text
- View/download PDF
211. The “second set” method for assessment of immunogenicity of heart valves
- Author
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Krasovskaya, S. M., Milovanova, Z. P., Dzemeshkevich, S. L., and Sychenikov, I. A.
- Published
- 1983
- Full Text
- View/download PDF
212. Enzymic degumming of pineapple and pineapple mill juices
- Author
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Chenchin, K., Yammamoto, H. Y., and Yugawa, A.
- Subjects
- *
ENZYMES , *PINEAPPLE juice - Published
- 1984
- Full Text
- View/download PDF
213. Effect of enzyme treatment of apple pulp with a commercial pectinaseand cellulase on the volatiles of the juice
- Author
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Drawert, F., Steiger, G., Schreier, P., and Mick, W.
- Subjects
- *
ENZYMES - Published
- 1978
214. The Effect of Storage, Processing and Enzyme Treatment on the Microstructure of Cloudy Spartan Apple Juice Particulate
- Author
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McKenzie, D. L. and Beveridge, T.
- Subjects
body regions ,storage ,enzyme treatment ,blanchung ,Apple juice ,post-harvet refrigeration ,microstructure ,juice particles ,polyglacturinase ,processing ,spartan apples ,Food Science - Abstract
The effect of blanching, post-harvest refrigerated (4C) storage and enzyme treatment with poly-galacturonase on the microstructure of Spartan apple juice was examined by thin sectioning and negative staining transmission electron microscopy. Particles were categrized as granules (3-54 nm), spheres (20-368 nm) and aggregates (12-2519 nm). Enzyme treatment with polygalacturonase significantly decreased granule size (P < 0.01). Storage of apples significantly decreased both granule size (p < 0.01) and aggregate length (p < 0.05) and also resulted in a web-like aspect in the microscopic appearance of juice particulate. The web-like aspect of the particulate was removed either through enzyme treatment with polygalacturonase or by blanching. Blanching of puree significantly increased granule (p < 0.05) and sphere size (p < 0.01) while significantly decreasing aggregate length (p < 0.01). In addition, blanching stabilized suspended particulate by what appeared to be the formation of a protective colloid which prevented particle aggregation through electrostatic repulsion.
- Published
- 1988
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