• 제목/요약/키워드: biological constituents

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한국(韓國) 야생차(野生茶)의 성분(成分)에 관(關)한 연구(硏究) - 제1보. 전질소(全窒素), 회분(灰分), 가용분(可溶分), 탄닌, 카페인 및 비타민 C 에 관(關)하여 - (Studies on the Chemical Constituents of the Tea Shoots in Native Tea Plant in Korea - Part 1. Total nitrogen, Ash, Water extract, Tannin, Caffeine and Vitamin C -)

  • 은종방;이종욱;김동연
    • Applied Biological Chemistry
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    • 제28권3호
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    • pp.202-208
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    • 1985
  • 한국(韓國) 재래(在來) 야생차(野生茶)의 유연성(類緣性) 조사(調査)로 형질(形質)이 다른 용장(龍欌) 차엽(茶葉)과 와운(臥雲) 차엽(茶葉), 그밖의 8개소(個所)의 야생차엽(野生茶葉)(일반차엽(一般茶葉)) 및 일본(日本)의 우량(優良) 녹차(綠茶) 품종(品種)인 Yabukita의 유엽(幼葉)을 각각(各各) 채엽(採葉)하여 차(茶)의 품질(品質)을 좌우(左右)하는 중요(重要)한 화학(化學) 성분(成分)인 전질소(全窒素), 회분(灰分), 가용분(可溶分), 탄닌, 카페인 및 비타민 C를 분석(分析) 비교(比較)한 결과(結果)는 다음과 같다. 1) 전질소(全窒素) 량(量)은 대죽(大竹) 차엽(茶葉)이 6.05%로 가장 많았고 용장(龍欌) 차엽(茶葉)이 4.94%로 가장 적었으며 일반차엽(一般茶葉)의 평균치(平均値)는 5.50%, 와운(臥雲) 차엽(茶葉)은 5.70%이고 Yabukita 차엽(茶葉)은 5.81%였다. 2) 회분(灰分) 량(量)은 군유산(軍有山) 차엽(茶葉)이 5.47%로 가장 많았고 태안사(泰安寺) 차엽(茶葉)이 4.94%로 가장 적었으며, 일반차엽(一般茶葉)의 평균치(平均値)는 5.15%이고 와운(臥雲) 차엽(茶葉)5.10%, 용장(龍欌) 차엽(茶葉) 4.97%, Yabukita 차엽(茶葉)은 5.18%였다. 3) 가용분(可溶分) 량(量)은 태안사(泰安寺) 차엽(茶葉)과 Yabukita 차엽(茶葉)이 각각(各各) 48.45%로 가장 많았고 대죽(大竹) 차엽(茶葉)이 44.10%로 가장 적었으며, 일반차엽(一般茶葉)의 평균치(平均値)가 46.78%, 와운(臥雲) 차엽(茶葉)이 47.75%, 용장(龍欌) 차엽(茶葉)이 47.78%였다. 4) 탄닌 량(量)은 용암산(聳岩山) 차엽(茶葉)이 15.67%로 가장 많았고 Yabukita 차엽(茶葉)이 10.41%로 가장 적었으며 일반차엽(一般茶葉)의 평균치(平均値)는 12.88%, 와운차엽(臥雲茶葉) 12.09%, 용장(龍欌) 차엽(茶葉)은 13.44%였다. 5) 카페인 량(量)은 대죽(大竹) 차엽(茶葉)이 2.89%로 가장 많았고 만덕산(萬德山) 차엽(茶葉)과 Yabukita 차엽(茶葉)이 2.43%로 가장 적었으며, 일반차엽(一般茶葉)의 평균치(平均値)는 2.72%, 와운차엽(臥雲茶葉)은 2.73%, 용장(龍欌) 차엽(茶葉)이 2.55%였다. 6) 총(總) 비타민 C 량(量)은 용암산(聳岩山) 차엽(茶葉)이 436.59mg%로 가장 많았고 군유산(軍有山) 차엽(茶葉)이 146.94mg%로 가장 적었으며 일반차엽(一般茶葉)의 평균치(平均値)는 264.59mg%, 용장(龍欌) 차엽(茶葉)이 223.10mg%, Yabukita 차엽(茶葉)이 256.49mg%였다. 7) 이상(以上)의 결과(結果)를 종합(綜合)할 때 용장(龍欌) 차엽(茶葉)은 일반차엽(一般茶葉)과 형질(形質) 뿐만 아니라, 성분(成分)도 다르므로 품종(品種)이 다른 수종(樹種)으로 추정(推定)되며 와운(臥雲) 차엽(茶葉)은 일반차엽(一般茶葉)과 형질(形質)은 다르나 성분상(成分上)의 비슷한 점으로 보아 동일계통(同一系統)의 변이(變異)된 대엽종(大葉種)으로 추정(推定)된다.

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랫드를 이용한 황기의 지상부 추출물에 대한 90일 반복경구투여 독성시험 (A 90 Day Repeated Dose-Oral Toxicity Study of Extracts from Astragalus membranaceus-Aboveground Parts in Rats)

  • 박영철;이지선;김동윤;손혜영;이정우;최유순;김광기;유창연;정일민;임무혁;이경재;최리나;심훈섭;임정대
    • 한국약용작물학회지
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    • 제21권6호
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    • pp.474-485
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    • 2013
  • Pharmacological studies and clinical practices have indicated that Radix Astragali, a dried root of Astragalus membranaceus possesses a lot of biological activities, including antioxidant, hepatoprotective, anti-diabetic, tonic, diuretic, antimicrobial, antiviral, and immunological activities. These biological activities approved by the modern pharmacological studies are mainly due to the constituents of Astragalus membranaceus including polysaccharides, saponins, flavonoids, amino acids, and trace elements. In resent, the main constituents in the root part showing a lot of biological activities has been isolated also from the aboveground parts such as leaves and sprouts in our laboratory. However, the safety evaluation for the aboveground parts of Astragalus membranaceus should be checked before expanding their application as one of food. In the study, a 90-day rat oral gavage study has been conducted with the extracts from Astragalus membranaceus-above-ground parts at doses of 1000, 3000, and 5000mg/kg/day. The following endpoints were evaluated: clinical observations, body weight, gross and microscopic pathology, clinical chemistry, and hematology. Based on the analysis of these endpoints, it was estimated that NOEL (no observed effect level) for male rats and NOAEL (no observed adverse effect level) for female rats are 5000mg/kg/day of the water-extracts from Astragalus membranaceus-aboveground parts.

Methylobacterium organophilum에 의한 메탄올로부터 생성되는 새로운 생물고분자 (New Extracellular Biopolymer Produced by Methylobacterium organophilum from Methanol)

  • 최준호;이운택;김정회;이준식
    • 한국미생물·생명공학회지
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    • 제17권4호
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    • pp.397-402
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    • 1989
  • Methylobacterium organophilum 이 탄소원과 에너지원으로서 메탄올로부터 생성하는 새로운 다당류계 생물고분자의 화학적 성질과 물성학적 성질을 관찰하였다. 분리정제한 다당류의 분자량은 약 4-5$\times$$10^6$ dalton 정도로 고분자량을 지니고 있다. 다당류의 화학적 조성은 건조중량의 66%가 탄수화물로 구성되어 있으며 이들의 88%가 환원당으로 구성되어 있다. 특이하게 본 고분자는 건조중량의 4.7%가 단백질로 구성되어 있다. 다당류는 glucose, galactose, 그리고 mannose을 몰비로 2:3:2 함유하고 있으며 탄수화물 이외에도 pyruvic acid, uronic acid, acetic acid 등을 함유하고 있다. 정제된 다당류를 증류수에 용해시켜 농도별로 점도를 측정한 결과 비뉴톤성 성질 중 pseudoplastic 성질을 보였으며 농도가 증가함에 따라서 겉보기점도 증가가 월등히 높았다. 동일한 1% 용액의 경우 K(consistency index)값을 비교하면 xanthan gum에 비해 약 10배정도 높은 18,000 cp 값을 나타내었다.

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Melanogenesis regulatory constituents from Premna serratifolia wood collected in Myanmar

  • WOO, SO-YEUN
    • 한국자원식물학회:학술대회논문집
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    • 한국자원식물학회 2019년도 춘계학술대회
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    • pp.21-22
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    • 2019
  • Melanin is a mixture of pigmented biopolymers synthesized by epidermal melanocytes that determine the skin, eye, and hair colors. Melanocytes produce two different kinds of melanin, eumelanin (dark brown/black insoluble pigments found in dark skin and dark hair and pheomelanin (lighter red/yellow). The biological role of melanin is to prevent skin damage by ultraviolet (UV) radiation. However, the overproduction or deficiency of melanin synthesis could lead to serious dermatological problems, which include melasma, melanoderma, lentigo, and vitiligo. Therefore, regulating melanin production is important to prevent the pigmentation disorders. Myanmar has a rich in natural resources. However, the chemical constituents of these natural resources in Myanmar have not been fully investigated. In the effort to search for compounds with anti-melanin deposition activity from Myanmar natural resources, five plants were collected in Myanmar. Extracts of these collected five plants were tested for anti-melanin deposition activity against a mouse melanoma cell line (B16-F10) induced with ${\alpha}$-melanocyte-stimulating hormone (${\alpha}$-MSH) and 3-isobutyl-1-methylxanthine (IBMX), and their anti-melanin deposition activities were compared with the positive control, arbutin. Among the tested extracts, the CHCl3 extracts of the Premna serratifolia (syn: P. integrifolia) wood showed anti-melanin deposition activities with IC50 values of $81.3{\mu}g/mL$. Hence, this study aims to identify secondary metabolites with anti-melanin deposition activity from P. serratifolia wood of Myanmar. P. serratifolia belongs to the Verbenaceae family and is widely distributed in near western sea coast from South Asia to South East Asia, which include India, Malaysia, Vietnam, Cambodia, and Sri Lanka. People in Tanintharyi region located in the southern part of Myanmar utilize the P. serratifolia, Sperethusa crenulata, Naringi crenulata, and Limonia acidissima as Thanaka, traditional cosmetics in Myanmar. Thanaka is applied in the form of paste onto skins to make it smooth and clear, as well as to prevent wrinkles, skin aging, excessive facial oil, pimples, blackheads, and whiteheads. However, the chemical constituents responsible for their cosmetic properties are yet to be identified. Moreover, the chemical constituents of P. serratifolia was almost uncharacterized. Investigation of the P. serratifolia chemical constituents is thus an attractive endeavor to discover new anti-melanin deposition active compounds. The investigation of the chemical constituents of the active CHCl3 extract of P. serratifolia led to isolation of four new lignoids, premnan A (1), premnan B (2), taungtangyiol C (3), and 7,9-dihydroxydolichanthin B (4), together with premnan C (5) (assumed to be an artifact), one natural newlignoid,(3R,4S)-4-(1,3-benzodioxol-5-ylcarbonyl)-3-[(R)-1-(1,3-benzo dioxol-5-yl)-1-hydroxy methyl]tetrahydro-2-furanone (6), and five known compounds (7-11)1,2). The structures of all isolated compounds were determined on the basis of their spectroscopic data and by comparison with the reported literatures. The absolute configurations of 1-3 and 5 were also determined by optical rotation and circular dichroism (CD) data analyses1). The anti-melanin deposition activities of all the isolated compounds were evaluated against B16-F10 cell line. 7,9-Dihydroxydolichanthin B (4) and ($2{\alpha},3{\alpha}$)-olean-12-en-28-oic acid (11) showed strong anti-melanin deposition activities with IC50 values of 18.4 and $11.2{\mu}M$, respectively, without cytotoxicity2). On the other hand, compounds 1-3, 5, and 7 showed melanogenesis enhancing activities1). To better understand their anti-melanin deposition mechanism, the effects of 4 and 11 on tyrosinase activities were investigated. The assay indicated that compounds 4 and 11 did not inhibit tyrosinase. Furthermore, we also examined the mRNA expression of microphthalmia-associated transcription factor (MITF), tyrosinase (TYR), tyrosinase-related protein-1 (TRP-1), and tyrosinase-related protein-2 (TRP-2). Compounds 4 and 11 down-regulated the expression of Tyr and Mitf mRNAs, respectively. Although the P. serratifolia wood has been used as traditional cosmetics in Myanmar for centuries, there are no scientific evidences to support its effectiveness as cosmetics. Investigation of the anti-melanin deposition activity of the chemical constituents of P. serratifolia thus provided insight into the effectiveness of the P. serratifolia wood as a cosmetic agent.

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Constituents of the Fruits of Rumex japonicus with Inhibitory Activity on Aldose Reductase

  • Kim, Jong-Min;Jang, Dae-Sik;Lee, Yun-Mi;Lee, Ga-Young;Kim, Jin-Sook
    • Journal of Applied Biological Chemistry
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    • 제51권1호
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    • pp.13-16
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    • 2008
  • Five anthraquinones, emodin (1), ${\omega}$-hydroxyemodin (2), chrysophanol-8-O-${\beta}$-D-glucoside (3), emodin-8-O-${\beta}$-D-glucoside (4), and physcion-8-O-${\beta}$-D-glucoside (5), and five flavonoids, kaempferol-3-O-${\beta}$-D-glucoside (6), quercetin (7), quercitrin (8), isoquercitrin (9), and (+)-catechin (10), were isolated from the EtOAc-soluble extract of the fruits of Rumex japonicus. The structures of 1-10 were identified by spectroscopic methods including NMR studies. This is the first report on the isolation of compounds 3-5 from this plant. The isolates were subjected to in vitro bioassays to evaluate their inhibitory activities on the rat lens aldose reductase (RLAR), among which two anthraquinones (1 and 4), and five flavonols (5-9) showed significant activities on RLAR.

Acacia catechu의 플라보노이드 성분 (Flavonoid Constituents of Acacia catechu)

  • 홍성수;최윤혁;서화진;강민정;신정혜;권오운;오좌섭
    • Journal of Applied Biological Chemistry
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    • 제58권2호
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    • pp.189-194
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    • 2015
  • 전통생약으로서 다양한 효능과 염색제로서 사용되어온 A. catechu의 식물화학적 성분연구를 위해 열수추출물 중 ethyl acetate 분획으로부터 9종의 flavonoid와 1종의 tannin을 단리하였으며, 이들의 물리화학적 성상과 spectral data로부터 구조를 확인한 결과 (+)-catechin (1), (-)-epicatechin (2), (+)-afzelechin (3), (-)-epiafzelechin (4), (+)-mesquitol (5), kaempferol (6), quercetin (7), quercetin 3-methyl ether (8) caryatin (9) 및 ellagic acid (10)로 각각 확인 동정하였다. 이들 화합물 중 caryatin (9)은 Acacia 속으로부터 처음으로 분리되었다.

민들레와 두종의 엉겅퀴의 Rat lens aldose reductase 억제활성 (Rat Lens Aldose Reductase inhibitory of Taraxacum mongolicum and two Cirsium species)

  • 정미정;허성일;왕명현
    • Journal of Applied Biological Chemistry
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    • 제51권6호
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    • pp.302-306
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    • 2008
  • 국화과 식물인 민들레, 엉겅퀴, 그리고 고려엉겅퀴를 대상으로 항당뇨 활성 측정 방법 중 하나인 흰쥐 수정체 aldose reductase 저해 활성을 측정하였다. 여러 부위별 추출물 중 민들레 지상부 메탄올 추출물이 $IC_{50}\;8.71\;{\mu}g/mL$로서 뛰어난 저해 활성을 보였다. 국화과 식물에서 분리된 대표적인 화합물인 silymarin과 민들레에서 분리한 luteolin(1)그리고 고려 엉겅퀴에서 분리된 syringin(2)을 대상으로 aldose reductase저해 활성을 측정한 결과 silymarin과 luteolin은 뛰어난 aldose reductase 저해 활성을 보였다.

Characterization of a Bioflocculant Produced by an Isolate, Bacillus megaterium G31

  • Chung, Sun-Ho;Kim, Hyung-Woo;Moon, Myeng-Nim;Yang, Young-Ki;Rhee, Young-Ha
    • 환경생물
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    • 제21권4호
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    • pp.358-365
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    • 2003
  • A bacterial strain capable of producing a novel bioflocculant was isolated from a biofilm sample and identified as Bacillus megaterium G31. The highest biopolymer yield was achieved when the organism was cultivated in a medium containing acetate as the sole carbon source and ($NH_4)_2HPO_4$as the nitrogen source. In kaolin suspension, the flocculating activity was highest at 170 mg I$^{-1}$ and decreased at the higher bioflocculant concentrations. The crude bioflocculant produced by the organism was purified by ethanol precipitation and gel permeation chromatography. The FTIR spectrum of the purified bioflocculant revealed that the bioflocculant might be a heterogeneous polysaccharide composed of hexosamines and neutral sugars. The analysis of sugar components of the bioflocculant using high performance anion-exchange chromatography showed that the sugar constituents of the bioflocculant were glucosamine, fucose, galactosamine, galactose, glucose, mannose in approximate molar ratio of 4 : 1 : 6 : 3 : 8 : 19. Its flocculating activity was stimulated by various cations. The bioflocculant was thermo-stable and retained 64% of its original activity after heating at $100^{\circ}C$ for 50 min.

재배지토양의 화학성이 인삼근중의 당류 및 saponin 함량에 미치는 영향 (Effects of the Chemical Properties of Field Soils on the Contents of Sugars and Saponin in Ginseng Roots)

  • 김동철;장상문;최정
    • Applied Biological Chemistry
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    • 제38권1호
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    • pp.72-77
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    • 1995
  • 품질이 좋은 인삼의 생산을 위한 재배지포장의 토양 및 영양관리를 위한 기초자료를 얻기 위하여, 인삼재배지토양의 화학성과 인삼근 중의 전당, 환원당, 유리당류, ginsenoside 및 saponin들의 상관관계를 조사하여, 인삼근의 품질에 미치는 영향을 조사하였다. 토양 중 $NO_3-N$함량은 인삼근 중의 전당 및 환원당의 함량과 고도의 부의 상관이 인정되었다. 토양 중 유기물함량은 인삼근 중의 당류와 ginsenoside계 성분들의 함량과 정의 상관이 인정되었으나, 토양 중 유효인산 및 치환성 양이온들의 함량은 부의 상관이 인정되었다.

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Pesticidal Constituents Derived from Piperaceae Fruits

  • Lee, Hoi-Seon
    • Journal of Applied Biological Chemistry
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    • 제48권2호
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    • pp.65-74
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    • 2005
  • Fungicidal, insecticidal, and mosquito larvicidal activities of piperidine alkaloids, pipernonaline and piperoctadecalidine, and isobutylamide alkaloids, pellitorine, guineensine, pipercide, and retrofractaminde A, derived from Piperaceae fruits were studied. Pipernonaline and piperoctadecalidine showed potent fungicidal activities against Puccinia recondita with 91 and 80% control values at 500 ppm. Against Phytophthora infestans, pipernonaline showed strong fungicidal activity with 91 and 80% control values at 1,000 and 500 ppm. $LD_{50}$ values of pipernonaline and piperoctadecalidine against Plutella xylostella were 125 and 95.5 ppm, respectively, and that of piperoctadecalidine against Tetranychus urticae was 246 ppm. Against larvae of Aedes aegypti and Culex pipiens pallens, $LD_{50}$ values of pipernonaline were 0.35 and 0.21 ppm, respectively. Highest larvicidal activities of pipercide and retrofractamide A were found against A. aegypti, A. togoi, and C. pipiens pallens. $LD_{50}$ values of pipercide and retrofractamide A were 0.10 and 0.039 ppm against A. aegypti, 0.26 and 0.01 ppm against A. togoi, and 0.004 and 0.028 ppm against C. pipiens pallens, respectively. Based upon these results and earlier findings, bioactive components derived from Piperaceae fruits may be valuable for development of useful lead product of possibly safer fungicidal, insecticidal, and mosquito larvicidal agents.