Abstract:
PURPOSE: Bacillus amyloliquefaciens CHO104 with antagonistic property and an antimicrobial compound produced thereby are provided. The novel antimicrobial compound can be useful in medicines, agricultural chemicals, foods, etc. CONSTITUTION: The microorganism Bacillus amyloliquefaciens CHO104(KCTC 18060P) isolated from the soil produces an antimicrobial compound. A microbial preparation containing Bacillus amyloliquefaciens CHO104 is prepared by culturing Bacillus amyloliquefaciens CHO104 in SDBP(soy dextrose beef ex. proteose peptone) medium at 30 to 35 deg. C. The novel antimicrobial compound, Amyloliquetone, is produced by the steps of: separating the supernatant of the cultured medium of Bacillus amyloliquefaciens CHO104; collecting an ethylacetate-soluble acidic·neutral fraction from the supernatant by adding 1N HCl; collecting an ethylacetate-soluble neutral fraction by adding 2 to 5% NaHCO3; subjecting the ethylacetate-soluble neutral fraction to an adsorption chromatography on silica gel to obtain an active fraction; and subjecting the active fraction to octadecylsilane column chromatography and HPLC, sequentially.
Abstract:
PURPOSE: Bacillus amyloliquefaciens CHO104 with antagonistic property and an antimicrobial compound produced thereby are provided. The novel antimicrobial compound can be useful in medicines, agricultural chemicals, foods, etc. CONSTITUTION: The microorganism Bacillus amyloliquefaciens CHO104(KCTC 18060P) isolated from the soil produces an antimicrobial compound. A microbial preparation containing Bacillus amyloliquefaciens CHO104 is prepared by culturing Bacillus amyloliquefaciens CHO104 in SDBP(soy dextrose beef ex. proteose peptone) medium at 30 to 35 deg. C. The novel antimicrobial compound, Amyloliquetone, is produced by the steps of: separating the supernatant of the cultured medium of Bacillus amyloliquefaciens CHO104; collecting an ethylacetate-soluble acidic·neutral fraction from the supernatant by adding 1N HCl; collecting an ethylacetate-soluble neutral fraction by adding 2 to 5% NaHCO3; subjecting the ethylacetate-soluble neutral fraction to an adsorption chromatography on silica gel to obtain an active fraction; and subjecting the active fraction to octadecylsilane column chromatography and HPLC, sequentially.
Abstract:
본 발명은 지초( Lithospermum erythrorhizon ) 뿌리의 에탄올추출물에 1-메틸-미오-이노시톨, 수크로오스, 1-케스토스, 니스토스등의 기능성 당화합물 존재확인 및 이들 물질의 분리방법에 관한 것이다. 지초뿌리를 에탄올 용매로 추출하여 얻어진 에탄올추출물을 농축하여 에탄올을 제거하고, 이어서 헥산과 에틸아세테이트로 세척한 다음, 메탄올로 용해하여 메탄올가용물을 얻은 후, 이 메탄올가용물을 실리카켈 흡착 컬럼 크로마토그라피, 옥타데실실란 컬럼 크로마토그라피, 세파덱스 LH-20 컬럼 크로마토그라피, GPC-HPLC등의 단계를 거쳐 최종적으로 4종의 화합물을 단리하였으며, FAB-MS, NMR 분석에 의해 상기 네가지 물질로 구조 결정하여, 이들 당화합물이 지초뿌리에 함유되어있음을 밝히고, 이들 당화합물의 분리방법을 제공한다.
Abstract:
본 발명은 지초( Lithospermum erythrorhizon ) 뿌리의 에탄올추출물에 1-메틸-미오-이노시톨, 수크로오스, 1-케스토스, 니스토스등의 기능성 당화합물 존재확인 및 이들 물질의 분리방법에 관한 것이다. 지초뿌리를 에탄올 용매로 추출하여 얻어진 에탄올추출물을 농축하여 에탄올을 제거하고, 이어서 헥산과 에틸아세테이트로 세척한 다음, 메탄올로 용해하여 메탄올가용물을 얻은 후, 이 메탄올가용물을 실리카켈 흡착 컬럼 크로마토그라피, 옥타데실실란 컬럼 크로마토그라피, 세파덱스 LH-20 컬럼 크로마토그라피, GPC-HPLC등의 단계를 거쳐 최종적으로 4종의 화합물을 단리하였으며, FAB-MS, NMR 분석에 의해 상기 네가지 물질로 구조 결정하여, 이들 당화합물이 지초뿌리에 함유되어있음을 밝히고, 이들 당화합물의 분리방법을 제공한다.
Abstract:
PURPOSE: A novel natural antimicrobial substance isolated from the stalk and leaf of Hovenia dulcis Thunb and an isolating method thereof are provided. Therefore, the novel natural antimicrobial substance, hovenidine B6, having pyridine structure can be found. CONSTITUTION: The novel natural antimicrobial substance, hovenidine B6 is isolated from the stalk and leaf of Hovenia dulcis Thunb by the steps of: heat-extracting the stalk and leaf of Hovenia dulcis Thunb; centrifuging the extract and freeze-drying the supernatant to obtain the extract powder; concentrating the methanol filtrate under reduced pressure to obtain methanol extract; adding a weak alkali buffer and ethylacetate into the methanol extract to divide a liquid fraction and an ethylacetate neutral fraction, and adding ethylacetate into the liquid fraction to obtain ethylacetate acid fraction; subjecting the above fractions to silica gel adsorption column chromatography using ethylacetate-methanol solution to obtain an active fraction; subjecting the active fraction to gel filtration chromatography using Sephadex LH-20 column; and subjecting the purified fraction to reverse HPLC using methanol-water solvent to isolate hovenidine B6.
Abstract:
본 발명은 천연항산화물질을 포함한 항산화 기능을 갖는 신선초조제물 및 제조에 관한 것이다. 보다 상세하게는 신선초를 열수로 추출한 추출물을 용매분획하여 얻어진 에칠아세테이트가용중성획분을 세파덱스 LH-20 컬럼 크로마토그라피 및 HPLC를 의해 루테올린 7- O -β-D-글루코피라노시드, 퀘서틴 3- O -β-D-갈락토피라노시드, 퀘서틴 3- O -β-D-글루코피라노시드, 퀘서틴 3- O -α-D-아라비노피라노시드, 캠펠로 3- O -α-D-아라비노피라노시드, 루테올린 3- O -β-D-람노피라노실(1→6)-7- O -α-L-글루코피라노시드를 분리하고 이들 물질의 구조결정은 MS, NMR 분석에 의해 이루어졌다. 이들 물질들은 DPPH 자유라디칼소거에 대한 항산화 활성을 갖고 있음이 검정되어, 이들 천연항산화물질을 포함한 항산화 기능을 갖는 신선초조제물은 산화에 의한 질병예방 및 노화억제효력을 갖는 기능성소재로서의 용도를 제공한다.
Abstract:
PURPOSE: Separation and production methods of caffeine, epigallocatechin, epicatechin, epigallocatechingallate, and epicatechingallate from tea leaves are provided, thereby simultaneously separating and producing the five kinds of materials. CONSTITUTION: Separation and production methods of caffeine, epigallocatechin, epicatechin, epigallocatechingallate, and epicatechingallate from tea leaves comprises the steps of: steaming tea leaves and drying them; heat-extracting the dried tea leaves or extracting the extract thereof with EtOH and freeze-drying it; subjecting the powdery extract to the sephadex column to obtain fractions of caffeine, epigallocatechin, epicatechin, epigallocatechingallate, and epicatechingallate; and subjecting the fractions to HPLC, removing an organic solvent and freeze-drying the HPLC fractions.
Abstract:
PURPOSE: A method for preparing a tea using the trunk and leaves of Hovenia dulcis and preparing a granule tea and a drink using their hot-water extract is provided. Thereby, the trunk and leaves of Hovenia dulcis is utilized well, which has fluent minerals, nutrition, effects to remove alcohol poisoning, and antibacterial and antioxidant effects. CONSTITUTION: A method for preparing a tea using the trunk and leaves of Hovenia dulcis comprises the steps of: (i) collecting the trunk and leaves of Hovenia dulcis from middle June to late July; (ii) heating with hot steam of 0.2kg/cm¬2 and 95deg.C for 20-45 minutes to inactivate the enzyme of leaves and trunk; (iii) cooling with cool air; (iv) destructing the leaves and trunk and drawing out water from them with a related device; (v) drying with a hot air dryer at 50-60deg.C for 10hours, and then pulverizing in 2mm size or less; and (vi) packing in tea bags. The prepared tea can be made into a granule tea and a drink using its hot-water extract.
Abstract:
본 발명은 진도홍주색소의 감별 방법에 관한 것으로, 지초를 사용하여 제조된 진도홍주를 분액여두를 이용하여 에칠아세테이트계 용매계로 분배하면 진도홍주의 홍색소가 이들 유기용매계로 분배되어지는 성질을 이용하여 감별하는 1단계 감별방법, 분광광도계의 의한 진도홍주색소의 분광학적 성질을 이용하여 감별하는 2단계 감별방법, 그리고 옥타데실실란 컬럼이 장착된 고성능액체크로마토그라피에 의해 진도홍주 홍색소 용출양상을 검토하여 감별하는 3단계 감별방법으로 구성된 진도홍주색소의 1, 2, 3단계 감별방법에 의해 진도홍주 홍색소가 지초유래의 색소인지를 간편하고도 정확하게 식별할 수 있는 감별방법을 제공한다.
Abstract:
PURPOSE: A natural antioxidant substance containing 4-hydroxy-3-methoxy benzoic acid, 4-hydroxy-3-methoxy cinnamic acid, quercetin-3-0-β-D-glucopyranoside and hovenidine B6 as a new natural antioxidant active material separated from Hovenia dulcis Thunb. is provided which is expected to be used as a material of food and medicine having an anti-aging function. CONSTITUTION: Leaves and stems of Hovenia dulcis Thunb. are extracted in water, freeze dried and then extracted in methanol, followed by solvent fractionation to produce an ethyl acetate acidic fraction and neural fraction. An active material contained in the extract is then purified with a purifying means such as silica gel column chromatography, chromatography with Sephadex LH-20, octadecylsilane column chromatography, a reversed-phase high-performance liquid chromatography or the like.