• 한국농림기상학회지
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• 제5권3호
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• pp.208-212
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• 2003

가로등과 보안등의 증가로 인한 야간조명의 확대와 야간 이동차량의 증가로 전조등 등 농경지 주변에 간헐적으로 조명이 이루어지고 있어 2000년부터 2001년까지 2년 동안 암기간과 야간조파가 벼와 콩의 출수 및 개화에 미치는 영향을 구명하고자 수행한 시험결과를 요약하면 다음과 같다. 12시간 암기 중 3시간마다 10분간 백열등(50∼60 lux)으로 조명한 야간조파 처리에 의하여 벼 생육은 두 품종 모두 암기처리 12시간에 비해 간장은 증가되었으며, 수당립수는 감소되었다. 벼의 출수는 야간조파시 암기처리 12시간에 비하여 일품벼 9일, 화성벼는 26일 지연되었으며, 12시간의 암기처리에 비하여 9시간 암기처리시 일품벼 47일, 화성벼는 41일 지연되었다. 야간조파에 의한 황금콩의 생육은 야간조파시 암기처리 12시간에 비해 경장파 절수가 증가되었으며, 협수는 감소되었고, 12시간의 암기처리에 비하여 9시간 암기처리시 경장 및 절수는 증가되었지만 협수는 감소되었다. 콩의 개화까지 소요일수는 야간조파시 암기처리 12시간에 비하여 4일 지연되었으며, 12시간의 암기처리에 비해 9시간 암기처리시 19일 지연되었다.

• Journal of Plant Biology
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• 제38권1호
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• pp.11-18
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• 1995

Mercury-induced changes in Chl a fluorescence induction kinetics of scratched barley leaf segments were dependent on the presence of light. By the treatment of 50$\mu$M HgCl2 under light condition, Fm and Fp were decreased. However, they were not significantly reduced under dark condition even after 2 h of mercury treatment. Under dark condition the decrease in variable fluorescence (Fv) after P transient was blocked within 20 min of the treatment. The analysis of fast fluorescence rise curve suggests that the inhibitory site of mercury under both light and dark conditions is not at QB binding site and the inhibition does not involve the increase in inactive PSII centers. Under light condition the decrease in Fp was partially recovered by addition of 50 $\mu$M NH2OH. These results suggest that a major inhibitory site of mercury under dark condition is at the reducing side of PSII and the site under light condition is at the oxidizing side of PSII possibly in addition to the one under dark condition. Under both light and dark conditions, energy-dependent quenching(qE) was alomost completely repressed within 20 min of mercury treatment and noticible change in Fo was not observed. The qE repression is probably due to the blockage of transthylakoid ΔpH formation.

• Journal of Microbiology and Biotechnology
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• 제29권9호
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• pp.1453-1459
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• 2019

Zeaxanthin is an important pigment in the photo-protection mechanism of microalgae. However, zeaxanthin epoxidase, an enzyme involved in the accumulation and conversion of zeaxanthin, has not been extensively studied in microalgae. In this work, we report the expression pattern of zeaxanthin epoxidase in Dunaliella tertiolecta (DtZEP) at different light and diverse salinity conditions. To confirm the responsiveness to light conditions, the ZEP expression pattern was investigated in photoperiodic (16 h of light and 8 h of dark) and continuous (24 h of light and 0 h of dark) light conditions. mRNA expression levels in photoperiodic conditions fluctuated along with the light/dark cycle, whereas those in continuous light remained unchanged. In varying salinity conditions, the highest mRNA and protein levels were detected in cells cultured in 1.5 M NaCl, and ZEP expression levels in cells shifted from 0.6 M NaCl to 1.5 M NaCl increased gradually. These results show that mRNA expression of DtZEP responds rapidly to the light/dark cycle or increased salinity, whereas changes in protein synthesis do not occur within a short period. Taken together, we show that DtZEP gene expression responds rapidly to light irradiation and hyperosmotic stress. In addition, ZEP expression patterns in light or salinity conditions are similar to those of higher plants, even though the habitat of D. tertiolecta is different.

• Journal of Ginseng Research
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• 제20권3호
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• pp.318-324
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• 1996

The effects of light on the growth and ginsenosides production were examined in the hairy roots of Panax ginsen C.A. Meyer induced by Agrobacterium rhizogines A4. The 9rowth of ginseng hairy roots in 1/2MS liquid medium was significantly decreased with an increment of light intensity (1,000~7,000 lux). The growth of hairy roots under 7,000 lux condition was decreased at 17% compared to the dark condition. The production of 7 ginsenosides in hairy root was very high in 3,500 lux condition. The production of ginsenoside-Rg, and Rf increased 3.3 and, 2.4 times respectively as compared to dark condition. The growth of hairy roots was inhibited by blue light, while ginsenosides production was increased. The sucrose demands of hairy roots was examined in light condition(3,500 lux). The growth of hairy roots in 1/2MS liquid medium with various sucrose concentrations(1~4%) was high in IVp sucrose, while ginsenosides production was high in 3% sucrose condition. The growth and ginsenosides production were high when hairy roots were cultured in dark condition for 1 week and then transferred to light condition(3,500 lux) for 4 weeks. It is suggested that ginsenosides production could be accelerated by light intensity of specific wavelength in cultures of ginseng hairy roots.

• 한국수소및신에너지학회논문집
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• 제16권4호
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• pp.315-323
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• 2005

The integrated or the two-stage (dark anaerobic and photosynthetic) fermentation processes were compared for the hydrogen production using purple non-sulfur photosynthetic bacteria, Rhodopseudomonas palustris P4. Cell growth, pH changes and organic acids and bacteriochlorophyll contents were monitored during the processes. Culture broth of Rps. palustris P4 exhibited dark-red during the photosynthetic culture condition, while yellow under the anaerobic condition without light. Rps. palustris P4 grown at the photosynthetic condition evolved 0.38 and 1.33 ml $H_2$/mg-dcw during the dark and the light fermentation, respectively, which were totally 1.71 ml $H_2$/mg-dcw at the two-stage fermentation. The rate of hydrogen production using Rps. palustris P4 grown under the dark anaerobic condition was 2.76 ml $H_2$/mg-dcw which consisted of 0.46 and 2.30 ml $H_2$/mg-dcw from the dark and the photosynthetic fermentation processes, respectively. Rps. palustris P4 grown under dark anaerobic conditions produced $H_2$ 1.6 times higher than that of grown under the photosynthetic condition. However, total fermentation period of the former was 1.5 times slower than that of the latter, because the induced time of hydrogen production during the photosynthetic fermentation was 96 and 24 hours when the seed culture was the dark anaerobic and photosynthetic, respectively. The integrated fermentation process by Rps. palustris P4 produced 0.52 ml $H_2$/mg-dcw(1.01 mol $H_2$/mol glucose), which was 20% of the two-stage fermentation.

• 생물환경조절학회지
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• 제26권2호
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• pp.146-150
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• 2017

본 연구는 식물공장에서 미나리 재배시 명/암주기와 암기시간 동안의 상대습도 조절이 미나리의 생육과 품질에 미치는 영향을 알아보고자 수행하였다. 정식 후 30일째에 수확하여 생육 및 품질을 비교하였을 때 상대습도 60/90%(명/암기) 처리가 60/60% 처리보다 지상부 생체중이 뚜렷이 증가하였다. 상대습도60/60% 처리에서 명기가 연장될수록 지상부 생체중이 증가하였지만 60/90% 처리에서는 16/8h 처리에서 지상부 생체중이 가장 높았으며, 20/4h, 22/2h 순이었다. 팁번의 발생은 상대습도 60/90%에서는 명/암주기 16/8h로 처리했을 때 1.4%로 매우 낮았으나, 명기 시간이 연장된20/4h, 22/2h 처리에서 각각 15.5% 30.3%로 급격히 증가하였다. 상대습도 60/60%에서는 명/암주기 16/8h에서도 팁번의 발생이 15.5%로 높았으며 20/4h, 22/2h 처리에서는 25% 이상 높게 나왔다. 줄기의 경도는 상대습도 60/90%, 명/암주기 16/8h 처리에서 가장 낮았다. 잎의 무기성분은 명기시간이 연장될수록 감소하였지만 Ca의 함량은 상대습도 60/60%, 명/암주기 22/2h 처리를 제외하고는 유의한 차이가 없었다.

• 생태와환경
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• 제33권1호통권89호
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• pp.9-22
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• 2000

본 연구에서는 남조류의 독성물질 배출 및 분해양상을 밝히고자 대청댐 지류인 옥천천의 스컴을 채취, 실험대상으로 하였다. Light와 dark 상태로 분리${\cdot}$배양한 배지에는 조사를 하는 동안 다른 영양염류는 첨가하지 않았다. 그 결과 세포내에서 microcystins의 총량은 세포수가 감소함에 따라 감소하였으며 Microcystis aeruginosa의 현존량과 비교하였을 때 light와 dark 상태의 경우 $r^{2}$값이 각각 0.96과 0.97로 높은 상관관계를 보였고 dark 상태에서 보다 더 빠른 감소추세를 보였다. 또한 세포에서 수체로 용존되는 microcystins의 량은 세포내에 존재하는 양의 극히 일부임을 확인 할 수 있었고 세포내에 분포하는 microcystins의 농도는 종류에 따라 차이를 보여 microcystin-RR>-LR>-YR의 순으로 존재하는 것으로 나타났다. 이러한 결과는 옥정호과 제천천을 대상으로 한 수심별 조사에서도 동일한 양상을 보였다. 수체에서 검출된 microcystins의 양은 점성물질의 양과 함께 light와 dark 상태에 따라 뚜렷한 차이를 보였으며 light의 경우 $r^{2}$값이 -0.75의 역의 상관관계를 보였다. 남조류 세포 및 microcystins에 대한 light와 dark 상태에서의 서로 다른 농도 결과는 배양 상태에 따른 미생물의 분해양상의 차이와 미생물에 대한 점성물질의 영향으로 추정된다.

• 한국식품과학회지
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• 제23권1호
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• pp.76-80
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• 1991

미강유 정제 부산물로부터 오리자놀을 분리하기위해, dark oil과 dark oil의 증류잔류물인 pitch로부터 용매분리법 이용하여 오리자놀을 분리하였다. 분리과정 중 방해물질인 왁스분은 dark oil과 acetone을 1 : 1(w/v)로 혼합하여, $0^{\circ}C$에서 침전시켜 제거하였고, 여기에서 얻어진 dewaxed dark oil에 8 part의 hexane을 섞어 저온분리하여 오리자놀함량이 51.3%인 농축물을 얻었다. 이 농축물에 methanol 20 part를 가하고 재결성하여 98.3%의 오리자놀결정물을 얻었다. Dark oil로부터 pitch를 제조하는 적정조건은$180^{\circ}C$와 $0.2{\sim}0.4torr$의 진공상태에서 2%(w/w)의 steam을 가하는 증류조건이 오리자놀의 파괴를 최소화 하였다. 이로부터 얻어진 pitch의 오리자놀순도와 회수율은 27.3%와 82.3%였다. Pitch에 hexane을 가하고 저온분리하여 오리자놀순도가 75.4%인 오리자놀결정물을 얻었으며 이 농축물에 methanol을 가한 후 재결정하여 순도가 99%인 결정물을 얻었다. 이상과 같은 저온윤리법을 이용하였을 때 오리자놀의 회수율은 dark oil 9.5%, pitch 28.5%로 나타났다.

• 한국자원식물학회지
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• 제2권1호
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• pp.235-241
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• 1989

The study was conducted to determine the Ms orthogonaL modia and the concentration of plant growth regulator for seed matura-tion and growth of rhizome from Cymbidium goeringii Germination waswell in dark condition, but the growth of rhizome was better un-der dark than under light condition in MS orthoTonal . Sucrose con-centration( 3 %) gave better results than higher ones(6%), andthe use of NAA(0.1 PPm) effect significant difference of seed ge-rmination .But the growth of rhizome was best in medium Containingsucrose concentration(3%) Ippm NAA and 1 PPm BA.

• Journal of Microbiology and Biotechnology
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• 제22권11호
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• pp.1471-1477
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• 2012

Carotenoids produced by non-photosynthetic bacteria protect organisms against lethal photodynamic reactions and scavenge oxygenic radicals. However, the carotenoid produced by Gordonia alkanivorans SKF120101 is coupled to reducing power generation. SKF120101 selectively produces carotenoid under light conditions. The growth yield of SKF120101 cultivated under light conditions was higher than that under dark condition. In the cyclic voltammetry, both upper and lower voltammograms for neutral red (NR) immobilized in intact cells of SKF120101 were not shifted in the condition without external redox sources but were commonly shifted downward by glucose addition and light. Electric current generation in a biofuel cell system (BFCS) catalyzed by harvested cells of SKF120101 was higher under light than dark condition. The ratio of electricity generation to glucose consumption by SKF120101 cultivated in BFCS was higher under light than dark condition. The carotenoid produced by SKF120101 catalyzes production of reducing power from light energy, first evaluated by the electrochemical technique used in this research.