• 식물조직배양학회지
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• 제28권4호
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• pp.215-219
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• 2001

팔레높시스 대량생산시 PLB 증식에 미치는 배지와 배양환경에 대해 조사하였다. PLB 증식량은 MS배지에서 높았지만, 증식된 PLB상태는 NDM배지가 더욱 양호하였다 천연첨가 물인 CW 10% 또는 사과와 감자의 사용은 PLB 증식효율을 향상시키는 데 필수적이었다. 배지내 지지물에 따른 PLB 증신률은 gelrite가 첨가된 고체배지가 흰색과 분홍색계통 모두 액체탈지면 배지보다 증식이 양호하였다. PLB 증식시 적정 sucrose 농도는 10g/L이며 농도가 높아질수록 PLB가 유식물체로 재분화되었고 저농도 일수록 증식과 유식물체의 재분화가 모두 억제되었다. PLB증식을 위한 적정 PPF와 온도는 각각 14.3 $\mu$mol.s$^{-1}$m$^{-2}$ , $25^{\circ}C$이었다.

• 화훼연구
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• 제17권1호
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• pp.9-14
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• 2009

밀토니아의 기내 대량생산을 위해 PLB의 유도와 증식을 위한 적정 배지 및 배양방법을 찾고자 본 실험을 수행하였다. 적정 배지는 MS 기본배지가 Hyponex 또는 VW배지보다 밀토니아의 PLB 유도가 우수하였다. PLB 증식 및 신초분화는 Hyponex 고체배지(Hyponex +바나나 20 g/L + sucrose $20g{\cdot}L^{-1}$, pH 5.2)가 MS 배지에 비해 더욱 효과적이었다. PLB로부터 신초분화에는 sucrose를 $10{\sim}20g{\cdot}L^{-1}$ 첨가하는 것이 효과적이었으나 30 g 이상의 농도에서는 유도된 신초수가 크게 감소하였다.

• 한국식품영양과학회지
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• 제21권4호
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• pp.418-422
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• 1992

효과적인 응유효소 생산을 위해 응유효소 생산 균주로 선정된 Mucor mucedo C-7을 밀기울 고체배지에 배양하여 최적 배양 조건을 검토하였다. 그 결과 밀기울에 대한 첨수량은 밀기울량에 100% 첨수하였을때 효소 생산이 가장 양호하였으며 배양 은도와 시간은 각각 3$0^{\circ}C$, 72시간이 가장 적당함을 알 수 있었다. 또 밀기울 배지에 증류수 대신 Macllvaine 완충용액 (pH4.5)을 첨가 하였을 경우 효소 생산은 현저히 증가하였으며 응유효소의 활성도 중류수를 첨수한 경우 보다 안정함을 알 수 있었다.

• Journal of Plant Biotechnology
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• 제5권3호
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• pp.187-191
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• 2003

This paper reported the establishment of mass production system of adventitious roots of Eleutherococcus sessiliflorus through the shake flask and bio-reactor culture. Induction of adventitious roots was started from the explants of germinated somatic embryos on half-strength Murashing and Skoog (MS) solid medium. The frequency of adventitious root formation was better in the explants comprising the basal hypocotyl parts than root explants alone. Among the different auxins tested (NAA, IBA and IAA), frequency of adventitious root induction was highest on medium with 0.5 mg/L NAA, and produced $16.3\pm1.9$ roots per explant. In shake-flask culture, deletion of $NH_4NO_3$ of MS medium was effective for induction of adventitious root compared with both full and half-strength MS media. Fresh weight increase of induced adventitious roots was performed well in medium with 0.5 mg/L IBA. When adventitious roots produced in shake-flask culture were transferred to 10-liter bioreactor, 5.5 times of fresh weight increase was gained after one month of culture. HPLC analysis revealed that the amount of eleutheroside E and E1 was higher in in vitro cultured adventitious roots than the 3 year-old field cultivated root barks of Eleutherococcus sessiliflorus. The content of eltutheroside B was much lower in adventitious roots than that of field cultivated one.

• Journal of the Korean Wood Science and Technology
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• 제33권5호통권133호
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• pp.92-98
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• 2005

This study was performed to get the basic information concerned to the optimum culture condition of Inonotus obliquus. Several solid media, PDA, MEA and Czapek-Dox, and three liquid media were adopted for the in vitro cultivation. Some main features of the fungal morphological characteristics under cultivation conditions were observed and described. Preliminary results showed that appearance of the mycelial mat, hyphal size and substrate pigmentation differed according to the media. The PDA medium was the most favorable substrate for the growth on solid culture, followed by MEA and Czapek-Dox media. Concerned to the addition of amino acids, 5 amino acids, such as alanine, alginine, isoleucine, leucine and threonine, enhanced to the mycelial growth. Isoleucine was shown the best fungal growth. An important morphological hyphal structure for the fungus, the setae, was found in abundance and diverse its shape and size. In liquid culture, fresh potato broth was the best growth stimulant of the fungus, followed by Malt extract and potato broth. Addition of yeast extract to the liquid media had improved the biomass, but not laccase production.

• Journal of Plant Biotechnology
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• 제8권1호
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• pp.21-25
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• 2006

Phragmites australis (reed) has received much attention as being one of the principle emergent aquatic plants for treating industrial and civil wastewater. Plant regeneration via plant tissue culture in p. australis was investigated. Three types of callus were identified from seeds on N6 medium plus 4.5 UM 2,4-dichlorophenoxyacetic acid (2,4-D). Yellow compact type showed the best redifferentiation, whereas white compact type and yellow friable were not competent to differentiate into plane. Solid medium culture was better than liquid suspension culture for enhancing callus growth when N6 medium supplemented with 4.5 ${\mu}M$ 2,4-D was used. Phytagel, as a gelling agent, was superior to agar in plant regeneration on N6 medium, supplemented with 9.4 ${\mu}M$ kinetin and 0.54 ${\mu}M$ $\alpha$-naphthaleneacetic acid (NAA). Transfer of the plantlets regenerated from kinetin and NAA-supplemented N6 medium to growth regulator-free MS medium enhanced the further development of the plantlets. Plantlets on subsequently grown to maturity when tansferred to potting soil. The regenerated plants exhibited morphologically normal. The system for plant regeneration of P. australis enables to propagate elite lines on a large scale for water purification in the ecosystem

• 식물조직배양학회지
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• 제26권3호
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• pp.157-161
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• 1999

본 연구는 글라디올러스 Topaz'를 재료로 액체진탕배양에 의한 캘러스의 증식효율을 향상시키기 위하여 수행되었다. 캘러스는 2,4-D 10mg/L가 첨가된 MS고체배지에 목자 외식체를 배양하여 유도하였다. 액체진탕배양에 의한 캘러스의 증식은 2,4-D 0.05 mg/L가 첨가된 MS배지를 사용하여 2$0^{\circ}C$, 16시간 일장하에서 배지를 100 mL 삼각플라스크에 20 mL 분주하고, 수평회전식 진탕배양기의 회전속도를 75 rpm으로 하였을 때 증식속도가 가장 빨랐다. 또한 동일 배지에서 캘러스의 계대배양 역시 가능하였다.

• 한국버섯학회지
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• 제11권2호
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• pp.87-91
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• 2013

느타리 버섯 No. 42균주를 5가지 배지에서 연구한 결과, 리그닌 분해효소인 Lac와 MnP는 생산되었으나 LiP는 생산되지 않았다. 실험한 본 균주의 경우 리그닌 분해효소인 Lac와 MnP의 생산에 밀기울이 관여하는 것을 확인 할 수 있었다. 액체배지에서는 GPYW에서 Lac(2.4 U/ml)와 MnP(3.6 U/ml)가 최대 생산됨을 알 수 있었으며 고체배지에서는 WMW에서 MnP(4.0 U/ml)가 최대 생산되었으며 W에서는 Lac(11.0 U/ml)가 최대 생산되었다.

• 한국축산식품학회지
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• 제30권2호
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• pp.236-242
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• 2010

The objective of this study was to investigate the potential of the application of kimchi LAB as starter culture in the production of fermented sausages. For this, the solid-state model media composed to simulate the substantial conditions of meat mixtures were fermented for 120 h after the treatment with different concentrations of kimchi (0.5, 1.0, 1.5, 3.0, and 5.0%) and lyophilized kimchi-powder (0.2 % and 0.5%). During the fermentation period, the growth of total viable cells and LAB, and the changes of pH and titratable acidity were investigated. The initial LAB counts ranged from 7.18 to 8.34 Log CFU/ mL for kimchi media and from 6.93 to 6.94 Log CFU/mL for kimchi-powder media depending on the added concentrations. The kimchi LAB in this study were not influenced by the immobilized condition for their adaptation and growth by showing no lag phase and thus acted similar as in the submerged medium. The initially increased counts reached around 9 Log CFU/ mL in 12 h independent of the concentrations of a ded kimchi. However, the growth and metabolic activity of kimchi-powder LAB were influenced by the immobilized condition. Supposedly, as the nutrient supply in solid-state depended solely on diffusion, these differences in the souring properties were caused by the LAB topography in the medium matrix. Nevertheless, the differences in the numbers of LAB between two media were less than 0.5 Log units and the pH drop in the solidstate batches was quite rapid and reached low values. Therefore, it can be assumed that kimchi and kimchi-powder LAB showed the utility as the substitute of commercial starter culture even without a rehydrating pretreatment.

• 생약학회지
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• 제25권1호
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• pp.28-30
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• 1994

The rate of growth and production of bioactive substances from Rehmannia glutinosa Liboschitz (Scrophulariaceae) were studied with the variation on the constituents of the culture media. The best growth was observed from MS basal medium containing 3.0 ppm NAA and 2.0 ppm kinetin. Carbohydrates (fructose, glucose and sucrose), phytosterols(${\beta}-sitosterol$, campesterol and stigmasterol) and carotenoid like substances were identified by GC-MS and TLC from the callus mass. However, catalpol was not detected from both solid and cell suspension cultures containing geraniol. Callus cultured Rehmannia glutinosa in the MS basal medium containing 0.1 ppm NAA and 0.1 ppm kinetin become differentiated to root.