• KSBB Journal
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• 제24권2호
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• pp.195-200
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• 2009

본 연구에서는 Eschscholtzia californica의 이차 대사산물인 benzo[c]phenanthridine alkaloids의 생산량을 향상시키기 위해 주요 영양성분인 질소원 농도를 조절하여 배지의 조성을 최적화하였다. 그 결과, 질산과 암모늄 이온의 초기 농도 비율은 세포 성장과 alkaloids 생산량 증대에 중요한 영향을 미치는 인자로서 작용함을 볼 수 있었다. 총 질소 농도를 standard MS배지의 총 질소원 농도와 동일하게 유지하고 (60 mM), 농도 비율 다양하게 조절했을 때, 세포 성장과 alkaloids 생산량은 질산과 암모늄 이온을 각각 단독으로 이용할 때 보다 효율적으로 증대함을 볼 수 있었다. 최대 성장 (9.84 g DCW/L)과 alkaloids 생산량 (60.72 mg/L)은 50 : 10의 비율에서 나타났으며, 농도 비율의 감소는 세포 성장을 억제하고 alkaloids 생산량을 감소시켰다. 또한, 질산과 암모늄 이온이 세포 성장과 alkaloids 생산량에 미치는 영향력을 보다 명확히 확인하기 위해 질산 이온과 암모늄 이온 농도를 각각 조절한 결과, 암모늄 이온이 증가할수록 alkaloids 생산량은 비슷하나, 세포 성장은 감소하였으며, 또한, 질산 이온의 농도를 증가시킬수록 세포 성장은 비슷한 값을 나타내었지만, alkaloids 생산량은 다양한 차이를 나타내었다. 본 실험에서 세포성장과 alkaloids 생산량에 적합한 농도는 50 : 25 (mol/mol) 비율에서 나타났으며, 본 실험을 통해 Eschscholtzia californica의 현탁 세포배양에서 질소원 농도의 조절을 통한 외부 환경조절은 세포 성장과 alkaloids 향상에 매우 효과적이며, 소량의 암모늄 이온의 첨가 시 질산 이온 농도조절은 세포 성장을 억제하지 않으면서 alkaloids 생산량을 유도하는데 적합한 이온임을 확인하였다.

• 한국응용과학기술학회지
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• 제29권2호
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• pp.248-256
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• 2012

Aza-indoles are important pharmacophores that have similar size and biological properties of indole. Here we have synthesized 4- and 7-azaindole tryptamines and showed that they are successfully incorporated in the biosynthesis of monoterepene indole alkaloids (MIAs) to form novel azaindole alkaloids by enzymatic reactions of strictosidine synthase(STR) and strictosidine glucosidase(SDG) monitored by UPLC/MS. By using HPLC equipped with a HPLC photo diode array(PDA) detector, each of the UV spectra of azaindole alkaloids was obtained and characterized. When hydrophilicity of azaindole alkaloids was compared, 4-azaindole alkaloids were more hydrophilic than 7-azaindole alkaloids.

• 약학회지
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• 제46권4호
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• pp.226-230
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• 2002

The Coptis Rhizome is known for containing a number of isoquinoline type alkaloids. Berberine, coptisine and palmatine are the major constituents of alkaloids. The alkaloids were isolated and determined by forming complex from Coptis japonica (Ranunculaceae). For the determination of these alkaloids, a new spectrophotometric method was developed with a simple and selective sample clean-up using thiocyanatocobaltate[II] complex ion. The absorbance of alkaloidal complex in l,2-dichloroethane solution was measured at 625 nm. A calibration curve for the alkaloids isolated from Coptis Rhizome was linear over the concentration range of 0.2-0.3 mg/mι. The method proved to be rapid, simple and reliable for the isolation and the determination of the alkaloids in Coptis Rhizome.

• 한국연초학회지
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• 제13권2호
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• pp.20-26
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• 1991

This study was carried out to develop the method of alkaloids analysis and investigate the kinds and contents of alkaloids in flue-cured, burley and oriental tobacco leaves using developed analytical method. The developed analytical method of alkaloids was as followed : Tobacco sample was treated with acid(pH 2∼3) and extracted with chloroform to remove chemical components except alkaloids. Sample solution was treated with alkali(pH 12∼ 13) and was extracted with chloroform to obtain alkaloids from sample solution. After extraction of alkaloids from tobacco leaves, alkaloids were separated and identified by GC, GC/MS using SE-54 fused silica capillary column. Nicotine, nornicotine, myosmine, 9-nicotyline, anabasine, anatabine, 2, 3-bipyridyl, cotinine, formyl nornicotine, acetyl nornicotine and formal anatabine were isolated and identified from the extracts of tobacco leaves. The contents of alkaloids were burley > flue-cured > oriental tobacco leaves, but oriental tobacco leaves were higher nornicotine, cotinine, formyl nornicotine and acetyl nornicotine contents than those of flue-cured tobacco leaves. The burley tobacco harvested in Korea was higher nornicotine contents by 2-6 times in the portions of cutter, leaf and tips position than that of burley tobacco(B3F) harvested in V. S. A.

• 식물조직배양학회지
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• 제26권2호
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• pp.77-83
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• 1999

Agrobacterium tumefaciens $A_4$T에 의해 형질전환된 사리풀 (Hyoscyamus niger L.)의 모상근으로부터 tropane alkaloids (scopolamine, hyoscyamine)의 생산성 향상을 위한 최적배지, 배양기간 및 탄수화물의 영향을 조사하였다. Tropane alkaloids의 생산성이 우수한 모상근 (HNl8, HN57)의 최적 배지는 SH배지이며, 모상근의 생장, tropane alkaloids 함량 및 생산성에서 조사한 6가지 배지보다 높게 나타났다. Tropane alkaloids생산을 위한 최적 배양기간은 HNl8 clone이 6주, HN57 clone은 5주로 나타났으며, 배양기간에 따라 scopolamine의 함량은 계속적으로 증가하는데 반하여 hyoscyamine의 함량은 일정 수준을 유지하는 것으로 나타났다. 두 세포주는 sucrose농도가 7%까지 증가할수록 생장률이 증가하는 반면, tropane alkaloids 함량은 감소하였으며, tropane alkaloids생산성은 3% sucrose처리구에서 가장 높게 나타났다. HN18 clone의 경우 최적 sucrose(3%)및 dextrose (2%)에서 유사한 tropane alkaloids 생산성을 나타내었다. 하지만 HN57 clone은 sucrose 처리구에 비하여 dextrose 처리구에서 매우 낮은 tropane alkaloids생산성을 나타내었다.

• 약학회지
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• 제20권3호
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• pp.125-129
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• 1976

The aim of this investigation was to develop a quantitative gas-liquid chromatographic method of analysis forhyosyamine and scopolamine, and to apply this method to the analysis of preparations. The trimethylsily(TMS) derivatives of the alkaloids were found to be far superior to the nonsilylating compounds in charomatagrams. Bis(trimethylsilyl) acetamide(BSA) was evaluated and found to be a good reagent for silyation of the alkaloids. The optimum derivatization conditions were heating the alkaloids in a closed tube at $70^{\circ)$ for 30 min with a 150 molar excess of BSA to the alkaloids were found to be alkaloids. Calibration curves for the two alkaloids were alkaloid. The standard deviations were 1.1% for hyoscyamine and 1.5% for scopolamine. The minimum detectable amount using the hydrogen flame ionization edtector was determined to be 2$\times$10$^{-11}$ moles of each alkaloid injected.

• Mass Spectrometry Letters
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• 제4권4호
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• pp.79-82
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• 2013

Various types of alkaloids observed in several herbal medicines were analyzed by electrospray ionization tandem mass spectrometry in positive ion mode. In the present study, MS/MS spectralpatterns were investigated for eight-types of alkaloids (aporpine, protoberberine, tetrahydroprotoberberine, benzylisoquinoline, protopine, phthalide, morpine, and bisbenzylisoquinoline). For aporpine- and protoberberine-type alkaloids, main fragmentations occurred at substituted groups on rigid ring structures, not showing ring fusion. Interesting fragmentations due to iminolization and retro-Diels-Alder (RDA) reaction were observed in MS/MS spectra of protopine- and tetrahydroprotobereberine-type alkaloids. Also, several types of fragmentations such as inductive cleavage and ${\alpha}$-cleavage, or bond cleavage between two ring structures were observed depending on their structural characteristics. These fragmentation patterns are expected to allow instant classification of the specific alkaloid type in various MS/MS spectra of alkaloids.

• 약학회지
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• 제17권3호
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• pp.137-140
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• 1973

Antimicrogbial activity of Veratrum alkaloids against Pityrosporum ovale. Trichopyton mentagrophytes, and Saccharomyces cerevisiae were investgated. Of the alkaloids tested, only jervaeratrum alkaloids exhibited antimicrobial activity. The most basic structural requirement for activity of jerveratrum alkaloids is mainly due to the introduction of an oxygen in ring C regardless of the difference in structural types. Glucoside is more active than alkamine, suggesting the assistance in the trasport processes.

• Natural Product Sciences
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• 제4권3호
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• pp.148-152
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• 1998

The extract from the bulbs of Pancratium maritimum L. afforded 12 alkaloids belonging to the skeletally six different groups of the Amaryllidaceae alkaloids. In this paper, the isolation and identification of (-)-N-demethyl-galanthamine (1), (+)-tazettine (2) and (-)-2-O-demethylmontanine (3) are described. Their structures have been determined by using extensive spectroscopic techniques. This is the first report describing the occurrence of 1 and 3 in this plant.

• 대한약학회:학술대회논문집
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• 대한약학회 2003년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.1
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• pp.251.2-251.2
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• 2003

The 2,3-trimethylene-4(3H)-quinazolinone and 2,3-tetramethylene-4(3H)-quinazolinone are not the only alkaloids isolated from plants. but are the part of a family of intriguing alkaloids including the bronchodilator vasicinone, anti-endotoxic isaindigotone, cytotoxic luotonins, antibiotic tryptanthrin, and antiinflammatory rutacearpine as well as related alkaloids. (omitted)