Abstract:
본 발명은 히루딘을 히루딘을 정제하는 방법을 제공한다. 본 발명의 방법은 조(粗) 히루딘액을 금속 이온으로서 구리이온을 사용하고 용리액으로서 인산염 완충액을 사용하는 금속이온 친화성 크로마토그래피를 이용하여 정제함을 특징으로 한다. 본 발명의 방법에 의하면 종래의 히루딘의 정제방법에 비해 저렴하고 간단하게 히루딘을 고순도로 정제할 수 있는 장점이 있다.
Abstract:
The tocopherol is purifyed by (a) adding mixed solvent of n- hexane and 50 % (v/v) methanol into the soybean oil distillate, (b) removing the sterol of the mixt. by filtering, cooling the filtered soln., and re-filtering, (c) methyl esterifying the mixt. from which sterol is removed, (d) recirculating esterified product at 100-130 deg.C and 10-3-10-4 torr in the molecular distillator to remove fatty acid methyl ester, (e) concentrating the obtd. soln. contg. 50-55 % tocopherol and dissolving in the lower alcohol (I), (f) adsorbing it into alkaline anion exchange resin, and purifying with the (I) contg. 5-10 % acetic acid, and (g) dissolving the purifyed tocopherol in the (I) and passing through cation exchange resin to obtain the final product.
Abstract:
A process for preparing prednisolone from hydrocortisone comprises: (a) pre-culturing arthrobactor simplex at 30 deg.C, pH 7.3 and 150-180rpm in the medium to obtain the starter; (b) innoculating the starter to the culture medium contg. 0-0.2gr. glucose, 0.1-1.0gr. casamino acid, 0.05-0.5gr. KH2PO4, 0.05-0.5gr. K2HPO4, 0.001-0.01gr. Mgcl2, 0.05gr. tween 80 and 100ml D.W., and culturing at 30-37 deg.C, pH 6-9 and 150-180rpm for 4hrs.; (c) adding hydrocortisone powder into the culture broth and culturing at the same condition for 28hrs to obtain the final product. The prednisolone is useful as an antiphlogistic.
Abstract:
PURPOSE: A novel confusion partner, the carboxypeptidase Y(CPY) propeptide for effective representation of polypeptide in E.coli, a recombinant vector and its transformed body are provided, by which small polypeptides(that is degradable easily in E.coli) can be produced stably. CONSTITUTION: A process for the preparation of novel confusion partner, the carboxypeptidase Y(CPY) propeptide, a recombinant vector and its transformed body comprises of: separating genomic DNA of Saccharomyces serebisiae, and processing PCR(Polymerase Chain Reaction) using the separated genomic DNA as a model chain(the primer used in this stage is synthesized by a DNA synthesizer); separating the cut fraction from agarose gel after cutting the fraction(fraction 1: 287 bp) gained by PCR with a restriction enzyme Nde I and Xho I, inserting into pET22b+ vector, and transforming to E.coli BL21(DE3) to represent; and inoculating the transformed E.coli and not-transformed E.coli to LB(yeast extract 0.5%, trypton 1%, NaCl 1%) liquid medium containing ampicillin, and confirming representation by adding IPTG(Isopropyl-beta-D-thiogalactopyranoside) while culturing at 37°C. The CPY propeptide is existed in the form of non-soluble coagulated body, but is dissolved in urea easily.
Abstract:
PURPOSE: Lipase purified with an organic solvent, its preparation method and chiral medical and pharmaceutical products using the lipase are provided, which lipase is improved in the enantiomeric ratio and is useful to prepare optically pure (S)-ketoprofen, (S)-ibuprofen and (S)-suprofen. CONSTITUTION: A lipase with improved enantiomeric ratio is prepared by adding 0.3-1.0 times by volume of an organic solvent to Candida rugosa lipase solution to collect the first-stage precipitate; adding 0.3-1.0 times by volume of an organic solvent based on the volume of the original lipase solution to the supernatant, to collect the second-stage precipitate; and 0.8-1.2 times by volume of an organic solvent based on the volume of the original lipase solution to the supernatant, to collect the precipitate. The organic solvent is acetone or isopropane.
Abstract:
PURPOSE: Provided is an aqueous and hetero phase separation segregate system consisting of a high molecular aqueous solution of polyethylene glycol and levan, to separate proteins in large quantity with low cost. And a protein separation system using the same is also provided. CONSTITUTION: An aqueous and hetero phase separation segregate system consisting of a high molecular aqueous solution of polyethylene glycol and levan is composed of the following steps of: (a) preparing polyethylene glycol-levan hetero phase segregation system; (b) searching phase diagram of polyethylene glycol-levan; and (c) searching distribution coefficient according to the change of concentration of salt and pH value.