Abstract:
The present compositions and methods relate to a beta-mannanase from Bacillus hemicellulosilyticus , polynucleotides encoding the beta-mannanase, and methods of make and/or use thereof. Formulations containing the beta-mannanase are suitable for use in hydrolyzing lignocellulosic biomass substrates, especially those comprising a measurable level of galactoglucomannan (GGM) and/or glucomannan (GM).
Abstract:
The present invention relates to probiotic bacteria strains which are able to hydrolyze prebiotic fibers. Further, the present invention relates to symbiotic compositions comprising at least one prebiotic fibers and at least one bacteria strain having at least an alpha-galactosidase enzyme and/or a beta-mannosidase enzyme. Further, the present invention relates to the use of said symbiotic compositions in food and/or pharmaceutical field. Finally, the present invention relates to food or pharmaceutical compositions comprising said symbiotic composition.
Abstract:
The present invention provides materials and methods for the solid-phase synthesis of oligosaccharides and glycopeptides. Such materials and methods include mutant glycosidase enzymes, or "glycosynthases", chemically-derivatized acceptor molecules, and specific solid support matrices.
Abstract:
The present invention provides sequences isolated from germinating seeds that can be used to control seed germination in plants. Such enzymes include seed-specific polygalacturonases, cellulases arabinosidases, xyloglucan endotransglycosylases (XET) and expansins.
Abstract:
Novel mannanases may be derived from e.g. Bacillus subtilis strain 168 or may be encoded by polynucleotide molecules comprising a nucleotide sequence as shown in SEQ ID NO: 1. The mannanases are useful e.g. in cleaning or detergent compositions, for modifying plant material, and for treatment of cellulosic fibres.
Abstract translation:新型甘露聚糖酶可以衍生自例如, 枯草芽孢杆菌菌株168或可以由包含如SEQ ID NO:1所示的核苷酸序列的多核苷酸分子编码。 在清洁或洗涤剂组合物中,用于改性植物材料和用于纤维素纤维的处理。
Abstract:
The present invention relates to pharmaceutical preparations comprising Factor VIII, a sulfated glycosaminoglycan and a hyaluronidase for the non-intravenous administration in the therapy and prophylactic treatment of bleeding disorders. The invention further relates to the combined use of a Factor VIII, a sulfated glycosaminoglycan and a hyaluronidase for the treatment and prevention of bleeding disorders, and to a method for increasing the bioavailability after non- intravenous administration of Factor VIII by co-adminstration of a sulfated glycosaminoglycan and a hyaluronidase.
Abstract:
본 발명은 셀룰로시마이크로비움 속 HY-13(Cellulosimicrobium sp. HY-13) 균주로 부터 생산된 만난아제에 관한 것으로, 구체적으로 무척추동물로부터 분리한 셀룰로시마이크로비움 속 HY-13균주로부터 생산된 고활성의 신규한 만난아제 (mannanase)에 관한 것이다. 상기의 균주로부터 생산된 만난아제는 곡물 및 식물에 포함된 헤미셀룰로오스 중 만난을 분해하여 이를 이용한 가수분해물의 바이오 매스 전환 또는 사료 원료로의 이용 가치를 높이는데 사용할 수 있다.
Abstract:
A thermostable glycosidase enzymes derived from various thermococcus, staphylothermus and pyrococcus organisms is disclosed. The enzymes are produced from native or recombinant host cells and can be utilized in the food processing industry, pharmaceutical industry and in the textile industry, detergent industry and in the baking industry.
Abstract:
The present invention relates to a DNA sequence, which codes for endomannanase produced by fungi of the genus Trichoderma and transferred into a yeast or fungus strain induces that strain to produce endomannanase, as well as to a method for isolating genes coding for endomannanases. The invention also relates to vectors, yeast strains and fungal strains containing the DNA sequence. Furthermore, the invention provides an enzyme product containing at least one endomannanase, which contains at least one of the following endomannanases produced by fungi of the Trichoderma genus: an enzyme having mannanase activity and an isoelectric point (pI) of about 3.8, an enzyme having mannanase activity and a pI of about 4.1, an enzyme having mannanase activity and a pI of about 4.5, an enzyme having mannanase activity and a pI of about 5.4 and an enzyme having mannanase activity and a pI of about 6.5, the isoelectric points being determined by isoelectric focusing. The endomannanase enzyme and enzyme products according to the invention can be used for hydrolyzation of mannopolymers, in particular in connection with bleaching of lignocellulosic pulps.