배양용기 내 환기와 광도에 따른 도라지(Platycodon grandiflorum A. DC.) 기내 배양묘의 생장반응
The Growth Response of Balloon Flower(Platycodon grandiflorum A. DC.) Plantlets In Vitro as Affected by Air Exchanges and Light Intensity
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기내 배양환경을 조절하여 건전한 유식물체를 획득하기 위해 도라지를 무균발아시켜 shoot 부분을 NAA 0.1 mg/L가 첨가된 MS 기본배지에 치상한 후 배양용기의 뚜껑위에 membrane filter를 부착하여 환기횟수를 달리하고 광도를 33, 66, 99 μ㏖ m-2s-1로 처리하여 생장반응을 조사하였다. Membrane filter 부착구의 환기횟수는 4.9 h-1이었으며 미부착구는 0.1 h-1이었다. 환기횟수 4.9 h-1 처리구에서 0.1 h-1 처리구에 비해 전반적으로 생장이 양호하였으며 0.1 h-1에서는 광도가 증가할수록 생장이 저조한 반면 4.9 h-1 처리구에서는 광도의 증가에 따라 생장이 좋은 경향이었다. 동일한 광도에서 환기횟수 4.9 h-1 처리구는 0.1 h-1 처리구에 비해 생체중은 1.9배, 당 함량은 1.4배 이상 높았으며 환기횟수 4.9 h-1 처리구는 광도의 증가에 따라 생체중과 당 함량이 높아졌으나 0.1 h-1 처리구는 광도에 의한 효과가 인정되지 않았다. 함수율은 환기횟수 4.9 h-1 처리구에서 0.1 h-1 처리구에 비해 4.2~5.8%가 낮았으나 광도 처리에 의한 차이는 없었다. 동일한 광도에서 총 엽록소 함량은 환기횟수 4.9 h-1 처리구에서 0.1 h-1 처리구에 비해 0.27∼0.79 mg/g F.W.가 높았으며 환기횟수 0.1 h-1 처리구는 광도의 증가에 따른 효과가 나타나지 않았으나 환기횟수 0.1 h-1 처리구는 높은 광도에서 감소하였다. 환기횟수 4.9 h-1는 0.1 h-1에 비해 잎의 공변세포가 크고 주변 부세포가 잘 발달되어 있었다. 특히 PPF 99 μ㏖ m-2s-1에서 환기횟수 0.1 h-1는 부세포의 발달이 미흡하고 기공이 많이 열려 있는 상태인 반면 환기횟수 4.9 h-1는 부세포가 잘 발달된 잎을 지니고 있었다.
Abstract
Shoots of balloon flower (Platycodon grandiflorum A. DC.) derived from in vitro germinated seeds were cultured on MS medium containing 0.1 mg/L NAA under various photosynthetic photon flux (PPF) 33, 66, and 99 μ㏖ m-2s-1 with or without membrane filter. Number of air exchanges per hour (NAEH) of the culture vessel with membrane filter on the lid was 4.9 h-1 and that without membrane filter was 0.1 h-1. Plantlets grown in 4.9 h-1 NAEH showed greater growth than in 0.1 h-1 NAEH. According to increase of PPF, plantlets growth decreased in 0.1 h-1 NAEH while it increased in 4.9 h-1 NAEH. At the same PPF, fresh weight and sugar content in plantlets in 4.9 h-1 NAEH were above 1.9, 2.0 times higher than those in 0.1 h-1 NAEH, respectively. Also they were enhanced in 4.9 h-1 NAEH by increase of PPF whereas no significance in 0.1 h-1 NAEH. The percentage of water content of plantlets in 4.9 h-1 NAEH was 4.2~5.5% lower than those in 0.1 h-1 and no difference in PPF. The content of total chlorophyll in plantlets in 4.9 h-1 NAEH was higher 0.27~0.79 mg/g F.W. than that in 0.1 h-1 NAEH. By increase of PPF, it was decreased in 0.1 h-1 NAEH while had no significant difference in 4.9 h-1 NAEH. Guard and subsidiary cells of leaves in 4.9 h-1 NAEH were more developed than in 0.1 h-1 NAEH. Especially, in 99 μ㏖ m-2s-1, leaves in 0.1 h-1 NAEH had undeveloped subsidiary cells and wide open stomata whereas those in 4.9 h-1 NAEH had well-developed subsidiary cells.
참고문헌 (25)
- "Copper enzymes in isolated chloroplasts polyphenoloxidase in Beta vulgaris", ar(n di), pp.1~15 (1959)
- Choi JI, "Photosynthetic characteristics and chlorophyll content of Hedera canariensis and Ficus benjamina in response to photosynthetic photon fluxes and CO2 concentrations", 40, pp.627~630 (1999)
- Choi SR, "Effects of membrane filter and sucrose concentrations on the growth of balloon flower plantlets In Vitro", 31, pp.209~217 (2004)
- Chung JD, "Recent plant biotechnology Ⅰ" (1995), Kyungbuk Univ
- Acta Hort 289, "Acclimatization techniques of plants from in vitro", pp.291~300 (1991)
- Economou AS, "Influence of light duration and irradiance on micropropagation of a hardy deciduous azalea", 11, pp.146~149 (1986)
- Fujiwara K, "Fundamental studies on environments in plant tissue culture vessels Measurements of carbon dioxide gas concentration in closed vessels containing tissue cultured plantlets and estimates on net photosynthetic rates of the plantlets", pp.21~30 (1987)
- Hasegawa PM, "Propagation of asparagus through apex culture transplant ability of plants and cytohistological characteristics", pp.143~148 (1973)
- Jeong GW, "Autotrophic growth of Limonium spp Ocean Blue' plantlets in vitro as affected by PPF", 11, pp.115~120 (2002)
- Kim JS, "photosynthetic rate and stomatal function of Spathiphyllum in vitro as affected by PPF and NAEH", 42, pp.351~352 (2001)
- Kim JS, "Growth of hosta and syngonium in vitro as affected by photosynthetic photon flux and the number of exchange per hour of the culture vessel", 44, pp.13~16 (2003)
- Kim YH, "Autotrophic growth of Dendranthema grandiflorum R Bongwhang' plantlets in vitro as affected by PPF", 8, pp.56~66 (1999)
- Fujiwara K, "Environmental control in micropropagation", pp.1~13 (1991)
- Fujiwara K, "Fundamental studies on environments in plant tissue culture vessels Effects of stoppers and vessels on gas exchange rates between inside and outside of vessels closed with stoppers", pp.119~127 (1986)
- Kozai T, "Photosynthetic characteristics of Cymbidium plantlet in vitro", 22, pp.205~211 (1990)
- Kozai T, "Effects of the number of air changes per hour of the closed vessel and the photosynthetic photon flux on the carbon dioxide concentration inside the vessel and the growth of strawberry plantlets in vitro", 26, pp.21~29 (1998)
- Kwon SI, "Effects of growth regulators and culture environment on ex vitro rooting and acclimatization of apple rootstock in vitro propagated", 31, pp.133~138 (2004)
- Lee HS, "Structural characteristics of leaves and carbohydrate content of propagules grown at different culture conditions in Gerbera hybrida Beauty'", 28, pp.117~121 (2001)
- Lee N, "Effects of quantum flux density on photosynthesis and chloroplast ultrastructure in tissue-cultured plantlets and seedlings of Liquidambar styraciflua L", pp.637~641 (1985)
- "Absorption of light by chlorophyll solutions", pp.315~322 (1941)
- McCready RM, "Determination of starch and amylose in vegetables", 22, pp.1156~1158 (1950)
- Morris DL, "Quantitative determination of carbohydrates with drywood's anthrone reagent", pp.254~107 255 (1948)
- "Plant propagation through tissue cultures", pp.206~221 (1974)
- Paek KY, "Anatomical observation of vitrified and glaucous leaf from Rehmannia glutinosa plant produced in vitro", 24, pp.323~327 (1997)
- Read PE, "Environmental effects in micropropagation Handbook of Plant Cell Culture", pp.95~125 (1984), McGraw-Hill Pub
