참고문헌 (43)

1. Radulović, Niko S, Blagojević, Polina D, Miltojević, Ana B. α‐Linalool – a marker compound of forged/synthetic sweet basil (Ocimum basilicum L.) essential oils. Journal of the science of food and agriculture, vol.93, no.13, 3292-3303.

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2. Fischer, Ravit, Nitzan, Nadav, Chaimovitsh, David, Rubin, Baruch, Dudai, Nativ. Variation in Essential Oil Composition within Individual Leaves of Sweet Basil (Ocimum basilicum L.) Is More Affected by Leaf Position than by Leaf Age. Journal of agricultural and food chemistry, vol.59, no.9, 4913-4922.

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3. Tada, Hiromi, Murakami, Yoshie, Omoto, Toshio, Shimomura, Koichiro, Ishimaru, Kanji. Rosmarinic acid and related phenolics in hairy root cultures of Ocimum basilicum. Phytochemistry, vol.42, no.2, 431-434.

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4. Pirmoradi, Mohammad Reza, Moghaddam, Mohammad, Farhadi, Nasrin. Chemotaxonomic Analysis of the Aroma Compounds in Essential Oils of Two Different Ocimum basilicum L. Varieties from Iran. Chemistry & biodiversity, vol.10, no.7, 1361-1371.

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5. Sakalauskaitė, Jurga, Viskelis, Pranas, Dambrauskienė, Edita, Sakalauskienė, Sandra, Samuolienė, Giedrė, Brazaitytė, Aušra, Duchovskis, Pavelas, Urbonavičienė, Dalia. The effects of different UV‐B radiation intensities on morphological and biochemical characteristics in Ocimum basilicum L.. Journal of the science of food and agriculture, vol.93, no.6, 1266-1271.

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6. Bais, Harsh Pal, Walker, Travis S, Schweizer, Herbert P, Vivanco, Jorge M. Root specific elicitation and antimicrobial activity of rosmarinic acid in hairy root cultures of Ocimum basilicum. Plant physiology and biochemistry : PPB, vol.40, no.11, 983-995.

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7. Gang, David R., Beuerle, Till, Ullmann, Pascaline, Werck-Reichhart, Daniéle, Pichersky, Eran. Differential Production of meta Hydroxylated Phenylpropanoids in Sweet Basil Peltate Glandular Trichomes and Leaves Is Controlled by the Activities of Specific Acyltransferases and Hydroxylases. Plant physiology, vol.130, no.3, 1536-1544.

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8. Kintzios, Spiridon, Makri, Olga, Panagiotopoulos, Emmanuil, Scapeti, Maria. In vitro rosmarinic acid accumulation in sweet basil (Ocimum basilicum L.). Biotechnology letters. : a monthly journal for the rapid communication of results and developments in all aspects of biotechnology, vol.25, no.5, 405-408.

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9. Petersen, Maike, Simmonds, Monique S.J. Rosmarinic acid. Phytochemistry, vol.62, no.2, 121-125.

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10. Huang, Beibei, Yi, Bo, Duan, Yanbing, Sun, Lianna, Yu, Xiaojing, Guo, Jing, Chen, Wansheng. Characterization and expression profiling of tyrosine aminotransferase gene from Salvia miltiorrhiza (Dan-shen) in rosmarinic acid biosynthesis pathway. Molecular biology reports, vol.35, no.4, 601-612.

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11. Jin, Xiang, Liu, Peng, Yang, Fengchi, Zhang, Ya-hong, Miao, Danmin. Rosmarinic Acid Ameliorates Depressive-Like Behaviors in a Rat Model of CUS and Up-Regulates BDNF Levels in the Hippocampus and Hippocampal-Derived Astrocytes. Neurochemical research, vol.38, no.9, 1828-1837.

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12. Petersen, Maike, Szabo, Elisabeth, Meinhard, Juliane, Karwatzki, Barbara, Gertlowski, Claudia, Kempin, Bettina, Fu�, Elisabeth. Biosynthesis and accumulation of rosmarinic acid in suspension cultures ofColeus blumei. Plant cell, tissue and organ culture, vol.43, no.2, 89-92.

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13. Zhang, Shuncang, Ma, Pengda, Yang, Dongfeng, Li, Wenjing, Liang, Zongsuo, Liu, Yan, Liu, Fenghua. Cloning and Characterization of a Putative R2R3 MYB Transcriptional Repressor of the Rosmarinic Acid Biosynthetic Pathway from Salvia miltiorrhiza. PloS one, vol.8, no.9, e73259-.

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14. Song, Jie, Wang, Zhezhi. RNAi-mediated suppression of the phenylalanine ammonia-lyase gene in Salvia miltiorrhiza causes abnormal phenotypes and a reduction in rosmarinic acid biosynthesis. Journal of plant research, vol.124, no.1, 183-192.

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15. Petersen, Maike. Cytochrome P450-dependent hydroxylation in the biosynthesis of rosmarinic acid in Coleus. Phytochemistry, vol.45, no.6, 1165-1172.

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16. Vogt, T.. Phenylpropanoid Biosynthesis. Molecular plant = 分子植物 英文版, vol.3, no.1, 2-20.

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17. Ooi, Chai Theam, Syahida, Ahmad, Stanslas, Johnson, Maziah, Mahmood. Efficiency of different Agrobacterium rhizogenes strains on hairy roots induction in Solanum mammosum. World journal of microbiology & biotechnology, vol.29, no.3, 421-430.

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18. Moriguchi, K., Maeda, Y., Satou, M., Hardayani, N.S., Kataoka, M., Tanaka, N., Yoshida, K.. The complete nucleotide sequence of a plant root-inducing (Ri) plasmid indicates its chimeric structure and evolutionary relationship between tumor-inducing (Ti) and symbiotic (Sym) plasmids in rhizobiaceae. Journal of molecular biology, vol.307, no.3, 771-784.

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19. Filetici, P., Span�, L., Costantino, P.. Conserved regions in the T-DNA of different Agrobacterium rhizogenes root-inducing plasmids. Plant molecular biology, vol.9, no.1, 19-26.

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20. Georgiev, Milen I., Pavlov, Atanas I., Bley, Thomas. Hairy root type plant in vitro systems as sources of bioactive substances. Applied microbiology and biotechnology, vol.74, no.6, 1175-1185.

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21. Thwe, Aye Aye, Kim, Jae Kwang, Li, Xiaohua, Bok Kim, Yeon, Romij Uddin, Md, Kim, Sun Ju, Suzuki, Tatsuro, Park, Nam Il, Park, Sang Un. Metabolomic Analysis and Phenylpropanoid Biosynthesis in Hairy Root Culture of Tartary Buckwheat Cultivars. PloS one, vol.8, no.6, e65349-.

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22. Guillon, Stéphanie, Trémouillaux-Guiller, Jocelyne, Pati, Pratap Kumar, Rideau, Marc, Gantet, Pascal. Hairy root research: recent scenario and exciting prospects. Current opinion in plant biology, vol.9, no.3, 341-346.

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23. Guillon, Stéphanie, Trémouillaux-Guiller, Jocelyne, Pati, Pratap Kumar, Rideau, Marc, Gantet, Pascal. Harnessing the potential of hairy roots: dawn of a new era. Trends in biotechnology, vol.24, no.9, 403-409.

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24. Chaudhuri, Kuntal Narayan, Ghosh, Biswajit, Tepfer, David, Jha, Sumita. Genetic transformation of Tylophora indica with Agrobacterium rhizogenes�A4: growth and tylophorine productivity in different transformed root clones. Plant cell reports, vol.24, no.1, 25-35.

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25. Gharechahi, J., Khalili, M., Hasanloo, T., Salekdeh, G.H.. An integrated proteomic approach to decipher the effect of methyl jasmonate elicitation on the proteome of Silybum marianum L. hairy roots. Plant physiology and biochemistry : PPB, vol.70, 115-122.

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26. Sharafi, Ali, Hashemi Sohi, Haleh, Mousavi, Amir, Azadi, Pejman, Dehsara, Bahareh, Hosseini Khalifani, Bahman. Enhanced morphinan alkaloid production in hairy root cultures of Papaver bracteatum by over-expression of salutaridinol 7-o-acetyltransferase gene via Agrobacterium rhizogenes mediated transformation. World journal of microbiology & biotechnology, vol.29, no.11, 2125-2131.

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27. Kim, Yoojeong, Wyslouzil, Barbara E., Weathers, Pamela J.. Secondary metabolism of hairy root cultures in bioreactors. In vitro cellular & developmental biology. journal of the Tissue Culture Association. Plant, vol.38, no.1, 1-10.

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28. Espinosa-Leal, Claudia A., Puente-Garza, César A., García-Lara, Silverio. In vitro plant tissue culture: means for production of biological active compounds. Planta, vol.248, no.1, 1-18.

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29. Murthy, Hosakatte Niranjana, Lee, Eun-Jung, Paek, Kee-Yoeup. Production of secondary metabolites from cell and organ cultures: strategies and approaches for biomass improvement and metabolite accumulation. Plant cell, tissue and organ culture, vol.118, no.1, 1-16.

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30. Sharma, Poojadevi, Padh, Harish, Shrivastava, Neeta. Hairy root cultures: A suitable biological system for studying secondary metabolic pathways in plants. Engineering in life sciences, vol.13, no.1, 62-75.

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31. Zhou, Mei-Liang, Zhu, Xue-Mei, Shao, Ji-Rong, Tang, Yi-Xiong, Wu, Yan-Min. Production and metabolic engineering of bioactive substances in plant hairy root culture. Applied microbiology and biotechnology, vol.90, no.4, 1229-1239.

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32. Shiga, Tomomi, Shoji, Kazuhiro, Shimada, Hiroaki, Hashida, Shin-nosuke, Goto, Fumiyuki, Yoshihara, Toshihiro. Effect of light quality on rosmarinic acid content and antioxidant activity of sweet basil, Ocimum basilicum L.. Plant biotechnology, vol.26, no.2, 255-259.

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33. Park, Woo Tae, Yeo, Sun Kyung, Sathasivam, Ramaraj, Park, Jong Seok, Kim, Jae Kwang, Park, Sang Un. Influence of light-emitting diodes on phenylpropanoid biosynthetic gene expression and phenylpropanoid accumulation in Agastache rugosa. Applied Biological Chemistry = 한국응용생명화학회지, vol.63, no.1, 25-.

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34. Gerhardt, Karen E., Lampi, Mark A., Greenberg, Bruce M.. The Effects of Far‐red Light on Plant Growth and Flavonoid Accumulation in Brassica napus in the Presence of Ultraviolet B Radiation. Photochemistry and photobiology, vol.84, no.6, 1445-1454.

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35. HAN, L., DONG, B.c., YANG, X.j., HUANG, C.b., WANG, X.d., WU, X.j.. Effect of Light on Flavonoids Biosynthesis in Red Rice Rdh. Agricultural sciences in China, vol.8, no.6, 746-752.

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36. Kawoosa, Tabasum, Singh, Harsharan, Kumar, Amit, Sharma, Sunil Kumar, Devi, Kiran, Dutt, Som, Vats, Surender Kumar, Sharma, Madhu, Ahuja, Paramvir Singh, Kumar, Sanjay. Light and temperature regulated terpene biosynthesis: hepatoprotective monoterpene picroside accumulation in Picrorhiza kurrooa. Functional & integrative genomics, vol.10, no.3, 393-404.

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37. Koyama, K., Ikeda, H., Poudel, P.R., Goto-Yamamoto, N.. Light quality affects flavonoid biosynthesis in young berries of Cabernet Sauvignon grape. Phytochemistry, vol.78, 54-64.

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38. Vogt, Thomas, Ibdah, Mwafaq, Schmidt, Jürgen, Wray, Victor, Nimtz, Manfred, Strack, Dieter. Light-induced betacyanin and flavonol accumulation in bladder cells of Mesembryanthemum crystallinum. Phytochemistry, vol.52, no.4, 583-592.

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39. Wang, Y., Gao, L., Shan, Y., Liu, Y., Tian, Y., Xia, T.. Influence of shade on flavonoid biosynthesis in tea (Camellia sinensis (L.) O. Kuntze). Scientia horticulturae, vol.141, 7-16.

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40. Park, Nam Il, Li, Xiaohua, Suzuki, Tatsuro, Kim, Sun-Ju, Woo, Sun-Hee, Park, Cheol Ho, Park, Sang Un. Differential Expression of Anthocyanin Biosynthetic Genes and Anthocyanin Accumulation in Tartary Buckwheat Cultivars ‘Hokkai T8’ and ‘Hokkai T10’. Journal of agricultural and food chemistry, vol.59, no.6, 2356-2361.

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41. Li, Xiaohua, Kim, Yeon Bok, Uddin, Md Romij, Lee, Sanghyun, Kim, Sun-Ju, Park, Sang Un. Influence of Light on the Free Amino Acid Content and γ-Aminobutyric Acid Synthesis in Brassica juncea Seedlings. Journal of agricultural and food chemistry, vol.61, no.36, 8624-8631.

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42. SHEN, LIMING, FOSTER, JOYCE G., ORCUTT, DAVID M.. Composition and Distribution of Free Amino Acids in Flatpea (Lathyrus sylvestrisL.) as Influenced by Water Deficit and Plant Age. Journal of experimental botany, vol.40, no.1, 71-79.

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43. Wallace, William, Secor, Jacob, Schrader, Larry E.. Rapid Accumulation of γ-Aminobutyric Acid and Alanine in Soybean Leaves in Response to an Abrupt Transfer to Lower Temperature, Darkness, or Mechanical Manipulation. Plant physiology, vol.75, no.1, 170-175.

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