• 제목/요약/키워드: flower buds

검색결과 174건 처리시간 0.024초

In Vitro 시스템에 의한 화호형성 (In Vitro Flowering System)

  • 류장렬;이행순;이광웅
    • 한국식물학회:학술대회논문집
    • /
    • 한국식물학회 1987년도 식물생명공학 심포지움 논문집 Proceedings of Symposia on Plant Biotechnology
    • /
    • pp.213-237
    • /
    • 1987
  • In vitro flowering system may minimize the confounded influence of non-floral meristem parts of plants in studying the relationship of a given treatment and flowering responses. We have induced flower buds from plantlets regenerated from zygotic embryo-derived somatic embryos of ginseng, which circumvented the normal 2-year juvenile period before flowering. The result suggests that the adulthood of ginseng root explants in the experiment previously conducted by Chang and Hsing (1980; Nature 284: 341-342) is not prerequired to flowering of plantlets regenerated through somatic embryogenesis. We have also induced flower buds from elongated axillary brandches from cotyledonary nodes by culturing ginseng zygotic embryos, seedlings, and excised cotyledonary nodes. It was found that 6-benzyladenine (BA) supplemented to the medium was essential for flowering, whereas abscisic acid (ABA) was inhibitory. Gibberellic acid(GA3) was also required for flowering when ABA was present with BA in the medium. The results suggest that cytokinins, gibberellins, and inhibitors play primary, permissive, and preventive roles, respective-ly, in the induction of flowering of ginseng. Tran Thanh Van (1980; Int. Rev. Cytol., Suppl. IIA: 175-194) has developed the "thin cell layer system" in which the induction of shoots, roots, or flower buds from epidermal layer explants were controlled by culture conditions and exogenous growth regulators in the medium, Utilizing the thin cell layer system, Meeks-Wagner et al. (1989; The Plant Cell 1: 25-35) have cloned genes specifically expressed during floral evocation. However, the system is too tedious for obtaining a sufficient amount of plant materials for biochmical and molecular biological studies of flowering. We have developed a garlic callus culture system and one obvious advantaging over the thin cell layer system is that an abundant cells committed to develope into flower buds proliferate. When the above cells were compared by two-dimensional gel electrophoresis with those which have just lost the competence for developing into flower buds, a few putative proteins specific to floral evocation were detected. The garlic callus culture system can be further explored for elucidation of the molecular biological mechanism of floral evocation and morphogenesis.hogenesis.

  • PDF

작약(芍藥) 화뇌제거시기에 따른 근수량(根收量)과 Paeoniflorin함량(含量) 변화(變化) (Effects of Removing Time of Flower Buds on Root Yield and Paeoniflorin Content in Paeonia lactiflora Pallas)

  • 김기재;박준홍;유오종;신종희;박소득;최부술;여수갑
    • 한국약용작물학회지
    • /
    • 제6권3호
    • /
    • pp.193-197
    • /
    • 1998
  • 작약(芍藥)의 화뇌제거시기가 생육(生育), 건근수량(乾根收量) 및 Paeoniflorin함량(含量)에 미치는 영향을 구명코자 시험연구한 결과는 다음과 같다. 1. 작약 재배시(栽培時) 화뇌제거에 따른 경장은 무제거에 비하여 $7{\sim}9cm$정도 제거된 만큼 짧아졌으며, 경수와 경직경은 차이가 없었다. 2. 화뇌제거에 따른 뿌리수와 생근중은 제거시기가 빠를수록 증가하였으며 , 건근수량은 화뢰크기가 10mm정도 될 때 제거한 것이 1,647/10a으로 무제거에 비하여 27% 증수되어 가장 많았다. 3. 화뇌제거시기별 paeoniflorin 함량은 뿌리굵기 5mm와 10mm에서는 무제거와 일정한 경향이 없었고, 15mm이상부터는 화뢰를 일찍 제거한 것이 화뢰 무제거보다 증가되었다. 4. 잎, 줄기의 paeoniflorin 함량은 잎이 줄기보다 높았으며, 생육초기에 높고 후기로 갈수록 낮아졌는데, 화뢰를 제거한 것이 무제거에 비하여 높았다.

  • PDF

미숙화기와 액아에 의한 네오레게리아의 기내 번식 (In Vitro Propagation of Neoregeria carorinae cv. Tricolor from Immature Flowers and Lateral Buds)

  • 정향영;박봉규;유창재
    • 식물조직배양학회지
    • /
    • 제22권4호
    • /
    • pp.223-227
    • /
    • 1995
  • 네오게레리아의 대량번식을 위해 미숙화기와 액아를 배양하였으며, 배양에 적합한 재료 채취시기, 생장조절제 종류와 농도 및 배양방법이 부정아 형성 및 생장에 미치는 영향을 조사한 결과, 미숙화기는 화아분화 4주후에, 액아는 화아 분화 7주후에서 절취하여 배양하는 것이 부정아 형성률이 가장 높았다. 부정아 형성에 적합한 생장조절제 종류와 농도는 MS + BA 1 mg/L + BA 0.5 mg/L이었다. 고체배지가 액체배지보다 부정아 형성 및 생장에 더 효과적이었다. 발근에 적합한 생장조절제 종류와 농도는 NAA 1 mg/L이었다. 액체배지가 고체배지보다 신초의 발근 및 생장에 더 효과적이었다.

  • PDF

Effects of Temperature and Ethylene Response Inhibitors on Growth and Flowering of Passion Fruit

  • Liu, Fang-Yin;Peng, Yung-Liang;Chang, Yu-Sen
    • 원예과학기술지
    • /
    • 제33권3호
    • /
    • pp.356-363
    • /
    • 2015
  • This study examined the effects of different day/night temperature regimes or silver ion on growth and flowering of passion fruit 'Tai-nung No.1'. Low temperature treatment ($20/15^{\circ}C$) caused passion fruit cultivar 'Tai-nung No.1' to fail to flower. Flowering induction occurred within a temperature range of $20-30^{\circ}C$, with no significant difference in the days to first flower bud and the total number of flower buds between plants grown at $30/25^{\circ}C$ and $25/20^{\circ}C$. However, plants grown at $30/25^{\circ}C$ exhibited their first flower buds set on the higher nodes and had higher abortion rates of flower buds than those at $25/20^{\circ}C$. Plants grown at $30/25^{\circ}C$ had the most rapid growth and the shortest plastochron. We also evaluated the effect of the ethylene response inhibitors silver nitrate ($AgNO_3$) and silver thiosulfate (STS) on growth and flowering of potted passion fruit 'Tai-nung No.1', when they were exposed to low temperature conditions ($20/15^{\circ}C$) following chemical treatments ($AgNO_3$ or STS, at 0.5 or 1.0 mM). $AgNO_3$ and STS treatments induced flower formation and initial flower bud formation within approximately two weeks at $20/15^{\circ}C$ whereas non-treated control plants exhibited no flower formation. ACC content and activity of ACC oxidase in the leaves of passion fruit 'Tai-nung No.1'exposed to low temperature conditions ($20/15^{\circ}C$) were significantly inhibited by the ethylene inhibitor treatments. These results indicate that ethylene, which is produced under low temperature conditions, plays an important role in inhibiting flower formation in passion fruit.

Insilico Analysis for Expressed Sequence Tags from Embryogenic Callus and Flower Buds of Panax ginseng C. A. Meyer

  • Sathiyamoorthy, Subramaniyam;In, Jun-Gyo;Lee, Byum-Soo;Kwon, Woo-Seang;Yang, Dong-Uk;Kim, Ju-Han;Yang, Deok-Chun
    • Journal of Ginseng Research
    • /
    • 제35권1호
    • /
    • pp.21-30
    • /
    • 2011
  • Panax ginseng root has been used as a major source of ginsenoside throughout the history of oriental medicine. In recent years, scientists have found that all of its biomass, including embryogenic calli and flower buds can contain similar active ingredients with pharmacological functions. In this study, transcriptome analyses were used to identify different gene expressions from embryogenic calli and fl ower buds. In total, 6,226 expressed sequence tags (ESTs) were obtained from cDNA libraries of P. ginseng. Insilico analysis was conducted to annotate the putative sequences using gene ontology functional analysis, Kyoto Encyclopedia of Genes and Genomes orthology biochemical analysis, and interproscan protein functional domain analysis. From the obtained results, genes responsible for growth, pathogenicity, pigments, ginsenoside pathway, and development were discussed. Almost 83.3% of the EST sequence was annotated using one-dimensional insilico analysis.

Inhibition of TNF-α-Mediated NF-κB Transcriptional Activity by Dammarane-Type Ginsenosides from Steamed Flower Buds of Panax ginseng in HepG2 and SK-Hep1 Cells

  • Cho, Kyoungwon;Song, Seok Bean;Nguyen, Huu Tung;Kim, Kyoon Eon;Kim, Young Ho
    • Biomolecules & Therapeutics
    • /
    • 제22권1호
    • /
    • pp.55-61
    • /
    • 2014
  • Panax ginseng is a medicinal herb that is used worldwide. Its medicinal effects are primarily attributable to ginsenosides located in the root, leaf, seed, and flower. The flower buds of Panax ginseng (FBPG) are rich in various bioactive ginsenosides, which exert immunomodulatory and anti-inflammatory activities. The aim of the present study was to assess the effect of 18 ginsenosides isolated from steamed FBPG on the transcriptional activity of NF-${\kappa}B$ and the expression of tumor necrosis factor-${\alpha}$ (TNF-${\alpha}$)-stimulated target genes in liver-derived cell lines. Noticeably, the ginsenosides $Rk_3$ and $Rs_4$ exerted the strongest activity, inhibiting NF-${\kappa}B$ in a dose-dependent manner. SF and $Rg_6$ also showed moderately inhibitory effects. Furthermore, these four compounds inhibited the TNF-${\alpha}$-induced expression of IL8, CXCL1, iNOS, and ICAM1 genes. Consequently, ginsenosides purified from steamed FBPG have therapeutic potential in TNF-${\alpha}$-mediated diseases such as chronic hepatic inflammation.

뽕나무 화아의 기내배양에 있어서 생장조절물질이 기관분화에 미치는 영향 (Effects of Plant Growth substances on Organ Regeneration from in virto cultured Flower Buds of Mulberry(Morus alba L., Morus bombycis Koidz.))

  • 남혁우;문재유;김호락
    • 한국잠사곤충학회지
    • /
    • 제30권1호
    • /
    • pp.1-7
    • /
    • 1988
  • 뽕나무의 화아의 기내배양을 실시할 경우 배지종류 및 생장조절물질의 농도가 각 기관의 생장 및 분화에 미치는 영향을 조사한 결과를 요약하면 다음과 같다. 1. Murashige and Skoog 배지는 Greshoff and Doy 및 Wolter and Skoog 배지에 비하여 자웅화아의 생장에 양호한 결과를 나타내었으며 자화의 성장은 2.0ppm BAP 농도에서 양호하였다. 2. 자화 및 웅화의 화아를 가지고 있는 삽수를 7일간 삽목하여 발아시킨 후 배양한 구가 삽목을 하지 않고 직접 치상한 구보다 화아의 발육이 양호하였다. 3. 고농도 Kinetin과 저농도 IAA를 혼용 첨가한 M.S. 배지에서 생장이 양호하여 발화되었고 건전한 주두 및 약을 얻을 수 있었다.

  • PDF

네오레게리아 기내배양시 변이발생과 기외 생육 (Variation of the Regenerated Plantlets from in Vitro Culture of Neoregeria carorinae 'Tricolor' and in Vivo Growth of Regenerated Plantlets)

  • 정향영;한봉희;신학기;김의영
    • 식물조직배양학회지
    • /
    • 제22권5호
    • /
    • pp.273-276
    • /
    • 1995
  • 네오레게리아(Neoregeria carorinae 'Tricolor')의 기내배양시 무늬소실을 줄일 수 있는 재료의 채취시기와 발근을 위하여 기내에서 처리된 오옥신이 온실에 이식된 식물체의 생육 및 개화에 미치는 영향에 관하여 실험한 결과, 화아분화 4주후(III단계)에 미숙화기를 배양한 것이 분화된 식물체 중 정상 식물체가 67%로 가장 많았고, 화아분화 직후 및 화아분화 5주후에 배양한 것은 모두 반입이 소실되었다. 미숙화기와 액아를 배양하여 나온 식물체중 정상식물체 획득율은 미숙화기 배양에서는 67%, 액아배양에서는 56.2%였다. 미숙화기를 배양하여 얻은 식물체가 액아를 배양하여 얻은 식물체보다 온실재배에서 생육이 월등이 좋았고, 개화율도 미숙화기를 배양하여 얻은 식물체는 27.8%이었으나 액아를 배양하여 얻은 식물체는 전혀 개화하지 않았다. IBA 0.5 mg/L가 첨가된 배지에서 발근시킨 식물체의 기외생육이 왕성하였으며, 기내에서 처리한 오옥신 종류와 농도는 온실에서 재배되고 있는 식물체의 변이에 영향을 미치지는 않았다.

  • PDF

HPLC-DAD-MS/MS를 이용한 금은화 생리활성 물질의 동시분석 (Simultaneous Analysis of Bioactive Metabolites from Lonicera japonica Flower Buds by HPLC-DAD-MS/MS)

  • 유성광;전주은;강경원;강삼식;신종헌
    • 약학회지
    • /
    • 제52권6호
    • /
    • pp.446-451
    • /
    • 2008
  • A high-performance liquid chromatography (HPLC) with diode array detector (DAD) and electrospray ionization mass spectrometry (ESI-MS) was established for the simultaneous determination of chlorogenic acid (1), sweroside (2), luteolin-7-O-glucoside (3), (E)-aldosecologanin (4) and 3,5-dicaffeoylquinic acid (5) from Lonicera joponica flower buds. The optimal chromatographic conditions were obtained on an ODS column (5 ${\mu}m$, 4.6${\times}$150 mm) with the column temperature $25^{\circ}C$. The mobile phase was composed of (A) water with 0.1% formic acid and (B) acetonitrile with 0.1% formic acid using a gradient elution, the flow rate was 0.3 ml/min. Detection wavelength was set at 250 nm. All calibration curves showed good linear regression ($r^2$>0.994) within test ranges. The developed method provided satisfactory precision and accuracy with overall intra-day and inter-day variations of 0.05${\sim}$1.95% and 0.15${\sim}$2.26%, respectively, and the overall recoveries of 97.71${\sim}$103.65% for the five compounds analyzed. The verified method was successfully applied to quantitative determination of the three types (phenolic compounds, iridoids and flavonoids) of bioactive compounds in 21 commercial L. japonica flower buds samples from different markets in Korea and China. The analytical results demonstrated that the contents of the five analytes vary significantly with sources.

The effect of plant extracts on the activity and the expression of MMPs (matrix metalloprotease) induced by UVA

  • Lee, Dong-hwan;Lee, Bum-chun;Yoon, Eun-jeong;Lee, Kyung-eun;Park, Sung-min;Pyo, Hyeong-bae;Choe, Tae-boo
    • 대한화장품학회:학술대회논문집
    • /
    • 대한화장품학회 2003년도 IFSCC Conference Proceeding Book II
    • /
    • pp.32-43
    • /
    • 2003
  • UV irradiation on a skin brings about the qualitative and quantitative alterations of the extracellular matrix. Repeated-UV irradiation suppressed the synthesis of collagen and activated the expression of the matrix metalloprotease (MMP). In this paper, on the purpose of development of novel anti-aging agents from natural sources, effects of several natural products on in vitro MMP-1 activity and UVA induced MMP-1 synthesis in human dermal fibroblast (HDF) culture were studied. We measured MMP-1 activities by fluorescence assay using gelatin as substrates. As a result, the extract of Dicentra spectabilis, and flower buds of Tussilago farfara showed strong inhibitory effect. Among them, the extract of flower buds of Tussilago fartara and Dicentra spectabilis inhibited MMP-1 activity by 92% and 87% at 0.05% (w/v). And UVA induced MMP-1 expression were analyzed by enzyme-linked immunosorbent assay (ELISA) and gelatin-based zymography in HDF culture. The extract of flower buds of Tussilago farfara and Dicentra spectabilis suppressed the UVA induced expression of MMP-1 by similar level of Vitamin C 200$\mu$M at 0.1% (w/v). These results suggest that the extract of Dicentra spectabilis, and flower buds of Tussilago farfara effectively prevent skin from the UV-induced photoaging. So the extracts are thought to have potential as effective raw materials for anti-aging cosmetics.

  • PDF