KR100671263B1 - 진세노사이드 알에이치1을 생산하는 방법 - Google Patents
진세노사이드 알에이치1을 생산하는 방법 Download PDFInfo
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- KR100671263B1 KR100671263B1 KR1020050031521A KR20050031521A KR100671263B1 KR 100671263 B1 KR100671263 B1 KR 100671263B1 KR 1020050031521 A KR1020050031521 A KR 1020050031521A KR 20050031521 A KR20050031521 A KR 20050031521A KR 100671263 B1 KR100671263 B1 KR 100671263B1
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- ginsenoside
- bifidobacterium
- ginseng
- microorganisms
- int57
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P19/00—Preparation of compounds containing saccharide radicals
- C12P19/44—Preparation of O-glycosides, e.g. glucosides
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H17/00—Compounds containing heterocyclic radicals directly attached to hetero atoms of saccharide radicals
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J17/00—Normal steroids containing carbon, hydrogen, halogen or oxygen, having an oxygen-containing hetero ring not condensed with the cyclopenta(a)hydrophenanthrene skeleton
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P33/00—Preparation of steroids
- C12P33/12—Acting on D ring
- C12P33/16—Acting at 17 position
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- Preparation Of Compounds By Using Micro-Organisms (AREA)
Abstract
Description
화합물 | R1 | R2 | R3 |
20(S)-프로토파낙사디올 형 | |||
진세노사이드 Rb1 | O-Glc(2-1)Glc | H | O-Glc(6-1)Glc |
Rb2 | O-Glc(2-1)Glc | H | O-Glc(6-1)Arap |
Rc | O-Glc(2-1)Glc | H | O-Glc(6-1)Araf |
Rd | O-Glc(2-1)Glc | H | O-Glc |
F2 | O-Glc | H | O-Glc |
Rh2 | O-Glc | H | OH |
화합물 K | OH | H | O-Glc |
O (Ⅰ) | O-Glc | H | O-Glc(6-1)Arap |
Y (Ⅱ) | OH | H | O-Glc(6-1)Arap |
Mc (Ⅲ) | OH | H | O-Glc(6-1)Araf |
Mc1 (Ⅳ) | O-Glc | H | O-Glc(6-1)Araf |
20(S)-프로토파낙사트리올 형 | |||
진세노사이드 Re | OH | O-Glc(2-1)Rha | O-Glc |
Rf | OH | O-Glc(2-1)Glc | OH |
Rg1 | OH | O-Glc | O-Glc |
Rg2 | OH | O-Glc(2-1)Rha | OH |
F1 | OH | OH | O-Glc |
Rh1 | OH | O-Glc | OH |
성분 | 리터당 함량 |
효모 추출물 쇠고기 추출물 고기 펩톤 아세트산 나트륨 제2인산나트륨 구연산 암모늄 황산 마그네슘 막레익산 활산 망간 덱스트로즈 트윈 80 | 10.0 g 10.0 g 10.0 g 5.0 g 2.0 g 2.0 g 1.0 ㎎ 0.1 ㎎ 0.05 ㎎ 20.0 g 10.0 ㎎ |
효소의 활성 | Int57 | SJ32 |
α-글루코시다제 | ++ | +++ |
β-글루코시다제 | +++ | +++ |
α-갈락토시다제 | +++ | +++ |
β-갈락토시다제 | +++ | +++ |
α-만노시다제 | - | - |
β-만노시다제 | - | - |
α-람노시다제 | - | - |
β-글루쿠로니다제 | - | - |
β-셀로바이오시다제 | - | - |
α-자일로시다제 | - | - |
β-자일로시다제 | +++ | +++ |
α-아라비노퓨라노시다제 | +++ | ++ |
α-아라비노피라노시다제 | +++ | ++ |
β-아라비노피라노시다제 | ++ | - |
미생물 | 화합물 K | |
농도(μM) | 함량(%) | |
Int57 | 1428ㅁ72 | 74ㅁ2 |
SJ32 | 884ㅁ40 | 53ㅁ2 |
미생물 | 화합물 K의 농도(μM) |
Int57 | 170ㅁ1 |
SJ32 | 165ㅁ1 |
Claims (7)
- 삭제
- 삭제
- 삭제
- 제 1항에 있어서, 상기 인삼 추출물은 수성용매 및/또는 유기용매를 추가로 포함하는 것을 특징으로 하는 방법.
- 제 5항에 있어서, 상기 수성용매는 pH 3 내지 8 범위의 포스페이트 완충용액 및 구연산 완충용액으로 구성된 군으로부터 선택되는 것을 특징으로 하는 방법.
- 제 5항에 있어서, 상기 유기용매는 메탄올, 에탄올 및 프로판올로 구성된 군으로부터 선택되는 저급 알코올, 톨루엔, 에틸아세테이트 및 클로로포름으로 구성된 군으로부터 선택되는 것을 특징으로 하는 방법.
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KR1020050031521A KR100671263B1 (ko) | 2005-04-15 | 2005-04-15 | 진세노사이드 알에이치1을 생산하는 방법 |
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KR1020050031521A KR100671263B1 (ko) | 2005-04-15 | 2005-04-15 | 진세노사이드 알에이치1을 생산하는 방법 |
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KR20060109187A KR20060109187A (ko) | 2006-10-19 |
KR100671263B1 true KR100671263B1 (ko) | 2007-01-19 |
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KR102441009B1 (ko) * | 2022-05-31 | 2022-09-06 | (주)아모레퍼시픽 | 인삼으로부터 화합물을 추출하는 방법, 상기 화합물을 포함하는 인삼 추출물 및 이를 포함하는 피부장벽 강화용 조성물 |
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