Abstract:
PURPOSE: A method for preparing L-ribose using a novel mannose-6-phosphoric acid isomerase is provided to obtain the L-ribose which is used as a synthesis starting material for a pharmaceutical product. CONSTITUTION: A mannose 6-phosphoric isomerase mutant is prepared by converting from 90th amino acid, N into D. A gene encoding the mutant has a base sequence of sequence number 5. A method for preparing the mutant comprises: a step of culturing a microorganism which is transformed by an expression vector including the mannose-6-isomerase gene; and a step of isolating the isomerase from the microorganism. The ribose is produced using L-ribulose as a substrate.
Abstract:
PURPOSE: A composition for preparing rear ginsenoside using beta-glycosidase and a method for preparing the ginsenoside are provided to quickly and selectively convert ginsenoside to other material. CONSTITUTION: A composition for preparing rare ginsenoside contains beta-glycosidase of high temperature. The rare ginsenosdie contains compound K, Y or Mc. The optically active temperature of the beta-glycosidase is 70-100°C. The beta-glycosidase is derived from Sulfolobus acidocaldarius. The beta-glycosidase has an amino acid of sequence number 4. The rear ginsenoside is obtained by reacting the beta-glycosidase with ginsenoside Rb1, Rb2, Rc or Rd and mixture in a reaction solvent at pH 4.5-7.0 and 70-100°C.
Abstract:
A method for preparing allose by using ribose 5-phosphate isomerase is provided to improve preparation yield by inhibiting production of by-products and improve preparation specificity to allose without addition of metal ions, so that the allose prepared is useful for inhibiting growth of cancer cells and damage of internal organs caused by ischemia. A D-allose is prepared by reacting D-psicose with ribose 5-phosphate isomerase isolated from Clostridium thermocellum, which is mass produced by (1) preparing a recombinant expression vector, pQE30/ribose 5-phosphate isomerase, containing ribose 5-phosphate isomerase gene, (2) culturing a transformed microorganism, Escherichia coli BL21(DE3) pQE30/ribose 5-phosphate isomerase, (3) inducing the expression of the ribose 5-phosphate isomerase gene, and (4) separating and purifying the expressed recombinant protein.
Abstract:
본발명은서열번호 1로기재되는아미노산서열로이루어진 12-지방산화효소; 또는상기 12-지방산화효소및 서열번호 2로기재되는아미노산서열로이루어진에폭사이드가수분해효소를포함하는수산화지방산, 헤폭실린 B 또는트리오실린 B 제조용조성물; 및이를이용한수산화지방산, 헤폭실린 B 또는트리오실린 B 제조방법에관한것이다.
Abstract:
본 발명은 10-하이드록시스테아르 산 (10-Hydroxystearic acid)의 생산방법에 관한 것으로, 더욱 상세하게는 리시니바실러스 후시포르미스 ( lysinibacillus fusiformis), 마크로코코스 카제리티쿠스 ( Macrococcus
acnes ), 스테노트로포모나스 말토필리아 ( Stenotrophomonas maltophilia ) 균 유래의 올레산 수화효소 (Oleate hydratase) 및 유전자를 포함하는 재조합 발현 벡터, 이로 형질전환 된 미생물을 이용하여 올레산 (oleate) 를 반응시켜 10-하이드록시스테아르 산을 고수율로 생산하는 방법이다. 본 발명에 따르면, 높은 특이성과 친환경적인 방법으로 산업품의 원료 물질인 10-하이드록시스테아르 산을 높은 수율로 생산할 수 있으며, 이렇게 생산된 10-하이드록시스테아르 산은 락톤(Lactone) 의 합성 시작물질로서 유용하게 사용될 수 있다.