• 한국버섯학회지
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• 제16권3호
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• pp.218-224
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• 2018

An auxin-producing bacterium, Klebsiella michiganensis Jopap-1, was isolated from a button mushroom bed in Buyeo-Gun, Chungcheongnam-Do. The strain Jopap-1 was classified as a novel strain of K. michiganensis based on a chemotaxonomic and phylogenetic analysis. The isolated K. michiganensis Jopap-1 was confirmed to produce indole-3-acetic acid (IAA), which is one of auxin hormones by TLC and HPLC analyses. The maximum concentration of IAA ($96.05mg\;L^{-1}$) was detected in the culture broth incubated in R2A medium containing 0.1% L-tryptophan for 48 h at $35^{\circ}C$ by HPLC quantity analysis. A negative relationship between IAA production and pH variation was estimated to show that the increase of IAA caused acidic pH in the culture. The effect of the supplement on L-tryptophan (precursor of IAA) production was observed to be highest at 0.1% concentration, but was significantly lowered above a concentration of 0.2%. To investigate the growth-promoting effects on the crops, the culture broth of E. michiganensis Jopap-1 was infected to water cultures and seed pots of mung bean and lettuce. Consequently, the adventitious root induction and root growth of mung bean and lettuce were observed to be 2.1 and 1.8 times higher than those of the control.

• 식물조직배양학회지
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• 제26권2호
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• pp.85-91
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• 1999

고구마의 정단분열조직을 배양하여 생장조절제의 종류와 농도 및 정단분열조직의 크기에 따른 다아체 증식효과를 조사하였다. NAA와 BA 혼용처리의 경우 0.1 ㎎/L NAA에 2.0 ㎎/L BA혼용처리에서 '목포 29호'와 '산천자'의 경우 배양 30일 후에 100% shoot분화율을 보였고, 뿌리발생률은 '목포 29호'는 66.7%, '산천자'는 69.2%였으며 줄기의 기부 부분에서 형성되었다. Cytokinin류인 kinetin과 BA 0.5∼4.0 ㎎/L 단독처리에서 다아체 분화율이 좋았으며 발달된 shoot의 대부분은 배양 60일 이내에 뿌리발생과 더불어 정상적인 식물체로 재분화되었다. 반면에 '금시'에서는 cytokinin류 단용처리에서 분화된 shoot가 캘러스화되어 정상적인 shoot를 생산하지 못하였다. 캘러스로 덮인 다아체의 shoot가 1∼2마디로 신장된 shoot를 분리하여 4.0 ㎎/L BA 또는 kinetin 처리구에 계대배양하였을 때, 분할된 shoot의 대부분이 줄기의 기부에 캘러스가 형성되면서 계대배양 30일 후에는 정상적인 shoot와 뿌리를 가진 재분화된 식물체의 생산이 가능하였다.

• 한국토양비료학회지
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• 제44권5호
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• pp.866-871
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• 2011

An auxin-producing bacteria (3YN11-02) was isolated from waste mushroom bed from Agaricus bisporus of Chungnam Buyeo-Gun area. The strain 3YN11-02 was identified as a novel species belongs to Rahnella aquatica by a chemotaxanomic and phylogenetic nalysis. The isolate was confirmed to produce indole-3-acetic acid (IAA) which is one of auxin hormone by TLC and HPLC analysis. When the concentration of IAA was assessed by performing HPLC quantity analysis, the maximal $290mg\;L^{-1}$ of IAA detected in ether fraction extracted from the culture filtrate which was cultured in R2A broth containing 0.1% tryptophan for 24 h at $35^{\circ}C$. The molecular weight of the main peak obtained by LC-mass analysis was correspondent well to 175, that of IAA. To investigate the growth promoting effect of crop, when the culture broth of R. aquatica 3YN11-02 was infected onto water culture and seed pot of mung bean, the adventitious root induction and root growth of mung bean were 2.0 times higher than control.

• Journal of Plant Biotechnology
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• 제6권1호
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• pp.39-43
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• 2004

A successful, efficient system for multiple shoot induction and plant regeneration of soybean (Glycine max) was established. Four soybean genotypes were compared for organogenic responses on various media cultured under light conditions. The adventitious shoots (98%, 2.6 shoots/cotyledon) directly from one-day-old cotyledon after germination induced by the hormone treatment and its efficiency was higher than any other conditions. The optimal medium for the induction of multiple shoots from cotyledon in Pungsannamulkong(shoot formation rate, 98%), Lx 16 (83%) and IIpumgeomjeongkong(63%) was MS medium supplemented with 2 mg/L BAP, but for Alchankong(75%), MS medium supplemented with 1mg/L zeatin and 1mg/L IAA, 3% sucrose, 4% Phytagel. Higher root induction (88%) was observed from the shoots placed on rooting medium (hormone-free MS basal). Plantlets were transferred onto the same medium supplemented with 1% activated charcoal for further development. With this treatment, regenerated plantlets were obtained within 7-8 weeks (shoot induction for 4 weeks, rooting and shoot elongation for 3-4 weeks).

• Plant Biotechnology Reports
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• 제4권2호
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• pp.101-107
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• 2010

An efficient plant regeneration system has been developed for figleaf gourd (Cucurbita ficifolia Bouch$\'{e}$), which is exclusively used as a rootstock for cucumber. The protocol is based on results obtained from a series of culture experiments involving different parts of the cotyledons and various media. The culture of cotyledon explants was critical for the enhancement of shoot regeneration frequency. The lower parts of the cotyledon excised at the plumule base were found to display a markedly enhanced production of adventitious shoots compared to other cotyledon regions. Culture in silver nitrate-supplemented Murashige and Skoog (MS) medium was not beneficial for shoot regeneration and suppressed root regeneration. Efficient shoot regeneration was obtained on MS medium containing 1.0 $mg\;l^{-1}$ zeatin and 0.1 $mg\;l^{-1}$ indole-3-acetic acid. Regenerated shoots successfully elongated and rooted in medium containing 0.1 $mg\;l^{-1}$ 1-naphthalene-acetic acid after 10-15 days of subculturing. The plantlets were satisfactorily acclimatized in a greenhouse and grew into normal plants without any morphological alterations.

• 한국자원식물학회지
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• 제24권3호
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• pp.280-285
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• 2011

In this study, we established a novel somatic embryogenesis and plant regeneration system through cell suspension culture of white dandelion (Taraxacum coreanum NAKAI.). Embryogenic calli could be initiated from leaf and root explants of sterile seedlings on solid Murashige and Skoog (MS) medium supplemented with 1.0 mg/L 2,4-dichlorophenoxyacetic acid (2,4-D) after 3-week cultures. To proliferate embryogenic calli rapidly, cell suspension culture was performed with transferred to liquid MS medium with various combinations of plant growth regulators (PGRs) including 2,4-D, ${\alpha}$-naphthalene acetic acid (NAA), indole-3-acetic acid (IAA), $N^6$-benzylamino purine (BAP), thidiazuron (TDZ), and kinetin. During suspension cultures, embryogenic calli not only greatly proliferated, but shoot organogenesis also simultaneously occurred from the surface of somatic embryos. Among them, TDZ at lower concentration, 0.1 mg/L produced the highest efficiency of somatic embryo formation and shoot organogenesis. Rooting of embryogenic calli with adventitious shoots was done on solid MS medium containing 0.1 mg/L NAA and 0.3% activated carbon. Nearly 80% of embryogenic calli with shoot organogenesis could be rooted normal. Well-rooted plantlets were transferred into pots under a greenhouse condition, and plants derived from this system appeared phenotypically normal.

• Journal of Ginseng Research
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• 제34권2호
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• pp.98-103
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• 2010

The medicinal plant Panax ginseng (P. ginseng) contains various phytosterols and bioactive triterpene saponins (ginsenosides). Squalene synthase catalyzes the first committed step in ginsenoside biosynthesis. Transgenic plants of P. ginseng were generated by introducing the squalene synthase gene derived from P. ginseng. Adventitious roots of the transgenic ginseng grew best in B5 medium, and 2 g of inoculum secured an optimal growth rate. Two phytohormones, indolebutyric acid and 1-naphtalene acetic acid, increased root growth and decreased ginsenoside production. Treatment with two selected elicitors, chitosan and jasmonic acid, and a precursor of the isoprenoid pathway, mevalonic acid, enhanced ginsenoside production and retarded ginseng growth rate.

• Journal of Microbiology and Biotechnology
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• 제18권11호
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• pp.1789-1791
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• 2008

This study was aimed (i) to develop an effective method for the purification of ginsenosides for industrial use and (ii) to compare the distribution of ginsenosides in cultured wild ginseng roots (adventitious root culture of Panax ginseng) with those of red ginseng (steamed ginseng) and white ginseng (air-dried ginseng). The crude extracts of cultured wild ginseng roots, red ginseng, and white ginseng were obtained by using a 75% ethanol extraction combined with ultrasonication. This was followed sequentially by AB-8 macroporous adsorption chromatography, Amberlite IRA 900 Cl anion-exchange chromatography, and Amberlite XAD16 adsorption chromatography for further purification. The contents of total ginsenosides were increased from 4.1%, 12.1%, and 11.3% in the crude extracts of cultured wild ginseng roots, red ginseng, and white ginseng to 79.4%, 71.7%, and 72.5% in the final products, respectively. HPLC analysis demonstrated that ginsenosides in cultured wild ginseng roots were distributed in a different ratio compared with red ginseng and white ginseng.

• 한국응용과학기술학회지
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• 제40권6호
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• pp.1445-1453
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• 2023

In 2022, the domestic production performance of functional cosmetics in South Korea reached 4.6 trillion won, accounting for 33.85% of the total cosmetics production. The number of functional cosmetics reviewed increased by about 7.5% from the previous year, totaling 974 items. Especially with the increasing importance of the skin barrier function due to skin sensitivity caused by various environmental pollutants, domestic cosmetic companies are showing interest in the development of new ingredients and products related to this area. This study aims to analyze academic research trends related to in vitro experiments for the development of cosmetics improving the skin barrier, to provide practical information for the cosmetic industry. The findings are as follows: Academic research mainly focused on the efficacy of natural ingredients in improving the skin barrier, but there is a significant lack of quantitative accumulation of research. For the development of skin barrier-improving cosmetic ingredients, efficacy evaluation indicators were set, including hyaluronic acid production, expression of filaggrin gene, loricrin, formation of cornified envelope (CE), and expression of ceramide synthesis enzyme genes. Moreover, effective cosmetic ingredients for improving the skin barrier included lemongrass and perilla leaf extracts, flavonoids, Lactococcus lactis subsp. lactis, Exosomelike Nanovesicles derived from apple callus, Eleutherococcus sessiliflorus, Acanthopanax sessiliflorus, Eleutherococcus gracilistylus, Acer okamotoanum extracts, Aloe vera adventitious root extract, ethanol extract of Aruncus dioicus, and organic solvent fraction of Dracocephalum argunense.

• 한국산림과학회지
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• 제42권1호
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• pp.67-73
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• 1979

단풍나무류(類)의 배축삽수(胚軸揷穗)에서 부정근(不定根)의 형성기원(形成基源)을 구명(究明)하기 위하여 단풍나무, 아기단풍나무 및 은단풍나무등의 종자(種子)를 파종(播種)하여 10일후(日後)에 얻은 길이 5cm의 배축삽수(胚軸揷穗)를 증류수(蒸溜水)에 꽂아 발근(發根)한 개체(個體)를 취(取)하여 발근부위(發根部位)를 microtom으로 절단(切斷)하여 Safranin-Fast green 이중염색(二重染色)을 하여 검경(檢鏡)하였던 바 그 결과(結果)를 요약(要約)하면 다음과 같다. 1. 단풍나무류(類) 배축삽수(胚軸揷穗)의 횡단면(橫斷面)의 구조(構造)는 외측(外側)으로부터 표피(表皮), 피층(皮層), 유관속(維管束) 및 수(隨)로 구성(構成)되어 있으며, 유관속(維管束)은 은단풍나무는 다원형(多原型), 단풍나무와 아기단풍나무는 4원형(原型)으로서 환상(環狀)을 이루고 있다. 2. 근원기(根原基)의 형성(形成)은 은단풍나무는 사부유조직(篩部柔組織) 및 유관속간유조직(維管束間柔組織)으로부터, 단풍나무와 아기단풍나무는 유관속간유조직세포(維管束間柔組織細胞)가 사부세포(篩部細胞)와 관련(關聯)하여 이루어지며, 삽수(揷穗)의 기부단면(基部斷面)에 callus의 형성(形成)은 없었다. 3. 단풍나무의 배축삽수(胚軸揷穗)는 대부분(大部分) 유조직(柔組織)으로서 세포(細胞) 분열능력(分裂能力)이 왕성(旺盛)하며, 형성(形成)된 근원기(根原基)는 계속(繼續) 부정근(不定根)으로 발달(發達)하여 유조직(柔組織)인 피층(皮層)과 표피계(表皮系)를 뚫고 나와 발근(發根)이 용이(容易)한 것으로 생각된다.