• Applied Biological Chemistry
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• 제51권1호
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• pp.1-5
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• 2008

질소비료의 과량 시용에 따른 시설원예지 토양 중 염류집적은 다양한 직물에 염류장애를 유발하여 국내농업에 심각한 문제가 되고 있다. 염류의 주성분은 질산염으로 필요이상의 질산이온을 제거하기 위하여 질산이온 흡수력이 크며, Enterobacter amnigenus GG0461로 동정된 토양세균을 시설원예 토양에서 분리하였다. 이 균주의 최적 생육 및 질산이온 흡수력을 조사하였을 때, GG0461 균주는 질산이온이 없는 조건에서 생육이 가능하나, 질산이온이 존재할 때 생육이 크게 촉진되었다. 또한, 염기성 조건에서 질산이온 흡수율이 증가하였으며, 성장과 질산이온 흡수 모두 pH 8-9에서 최대로 나타났다. 배지의 초기 pH를 8과 9로 조정하였을 때, 균주에 의하여 질산이온이 흡수됨에 따라 배지의 pH는 중성으로 감소하였다. 이러한 결과는 질산이온 흡수를 위한 주된 인자가 nitrate/proton antiporter임을 의미한다. 이것은 질산이온이 없는 조건에서 질산이온의 첨가 효과인 질산이온 흡수의 급격한 증가와 빠른 배지의 pH 감소 사실로도 확인되었다.

• Annals of Pediatric Endocrinology and Metabolism
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• 제23권4호
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• pp.204-209
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• 2018

Purpose: Growth hormone transduction defect (GHTD) is characterized by severe short stature, impaired STAT3 (signal transducer and activator of transcription-3) phosphorylation and overexpression of the cytokine inducible SH2 containing protein (CIS) and p21/CIP1/WAF1. To investigate the role of p21/CIP1/WAF1 in the negative regulation of the growth hormone (GH)/GH receptor and Epidermal Growth Factor (EGF)/EGF Receptor pathways in GHTD. Methods: Fibroblast cultures were developed from gingival biopsies of 1 GHTD patient and 1 control. The protein expression and the cellular localization of p21/CIP1/WAF1 was studied by Western immunoblotting and immunofluorescence, respectively: at the basal state and after induction with $200-{\mu}g/L$ human GH (hGH) (GH200), either with or without siRNA CIS (siCIS); at the basal state and after inductions with $200-{\mu}g/L$ hGH (GH200), $1,000-{\mu}g/L$ hGH (GH1000) or 50-ng/mL EGF. Results: After GH200/siCIS, the protein expression and nuclear localization of p21 were reduced in the patient. After successful induction of GH signaling (control, GH200; patient, GH1000), the protein expression and nuclear localization of p21 were reduced. After induction with EGF, p21 translocated to the cytoplasm in the control, whereas in the GHTD patient it remained located in the nucleus. Conclusion: In the GHTD fibroblasts, when CIS is reduced, either after siCIS or after a higher dose of hGH (GH1000), p21's antiproliferative effect (nuclear localization) is also reduced and GH signaling is activated. There also appears to be a positive relationship between the 2 inhibitors of GH signaling, CIS and p21. Finally, in GHTD, p21 seems to participate in the regulation of both the GH and EGF/EGFR pathways, depending upon its cellular location.

• 한국식품위생안전성학회지
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• 제12권3호
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• pp.181-187
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• 1997

Lactobacillus acidophilus NCFM, Lactobacillus casei YIT 9018, Bifidobacterium longum 8001, and Bifidobacterium longum 8025 at the level of 106 cfu/$m\ell$ were cultured with 104 cfu/$m\ell$ of Escherichia coli O157:H7 KSC 109 or Salmonella typhimurium ATCC14028, in order to verify the effects of lactic acid bacteria and bifidobacteria on the growth of the pathogens. In the mixed culture of lactic acid bacteria with E. coli O157:H7 KSC 109, Growth inhibition and atypical microcolonies of E. coli O157:H7 KSC 109 were observed. The pathogens inoculated grew for 5 hors (pH 5.3), by the time L. acidophilus NCFM reached the exponential growth phase, and then the surviving pathogens were decreased to 101 cfu/$m\ell$ after 35 hours. When L. caseiYIT 9018 was grown with the pathogens, they grew for 10 hours (pH 4.6), by the time L. casei YIT 9018 reached the end of exponential growth phase, and then the surviving pathogens were decreased drastically. Up to the stationary growth phase of lactic acid bacteria, L. acidophilus NCFM exhibited stronger inhibition against the pathogens than L. casei YIT 9018 did, which might be attributed to its faster growth. Likewise bifidobacteria inhibited the growth of the pathogens tested, bifidobaceria was weaker in the inhibitory activity than lactic acid bacteria. When Bifidobacterium longum 8001 was cultured with the pathogens, E. coli O157:H7 KSC 109 was gradually ingibited at the stationary growth phase of bifidobacteria, atypical microcolonies were formed on Levine EMB medium after 48 hours, and Salmonella grew up to 106 dfu/$m\ell$, then was drastically ingibited at the exponential growth phage of Bifidobacterium longum 8001. But when Bifidobacteriuam longum 8025 was cultured with the pathogens, the pathogens grew to the same level of Bifidobacteriuam longum 8025 was cultured with the pathogens, the pathogens grew to the same lever of Bifidobacteriuam longum 8025 after 10 hours, then the surviving pathogens were decreased drastically.

• Journal of Dairy Science and Biotechnology
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• 제14권2호
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• pp.195-206
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• 1996

Cholesterol assimilated by Lactobacillus acidophilus ATCC 43121 was not metabolically degraded in that most of it was recovered with the cells. Cells grown in the presence of cholesterol micelles and bile salts were more resistant to Iysis by sonication than those grown in their absence, suggesting a possible alteration of cellular membranes. Cholesterol assimilation occurred during growth at pH 6.0, the amount of which was more than that by cells grown without pH control. Cholesterol assimilated by cells was recovered in the membrane fractions of cells both grown at pH 6.0 and without pH control. The effect of unsaturated fatty acids on cholesterol assimilation was not clear, since there was no significant (P> 0.05) difference in the amount taken up from micelles prepared using L-${\alpha}$-phosphatidylcholine, dioleoyl or L-${\alpha}$-phosphatidylcholine, distearoyl. Without Tween 80, little, if any, cell growth or cholesterol uptake was observed. In the presence of 0.05% Tween 80, cholesterol uptake increased dramatically as did growth. However, as the amount of Tween 80 increased beyond 0.05%, cholesterol uptake decreased while the amount of growth remained the same.

• 상하수도학회지
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• 제27권1호
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• pp.69-76
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• 2013

Specific growth rate and removal rate of nitrogen and phosphorus of Chlorella sorokiniana, Chlorella vulgaris, Senedesmus dimorphus those are able to metabolite mixotrophically and have high nitrogen and phosphorus removal capacity were examined. Based on the results, one microalgae was selected and conducted experiments to identify the operating factors such as pH and aeration rate. The specific growth rate and phosphorus removal rate of C. sorokiniana significantly presented as $0.29day^{-1}$ and 1.65 mg-P/L/day, while the nitrogen removal rate was high as 12.7 mg-N/L with C. vulgaris. C. sorokiniana was chosen for appropriate microalgae to applying for wastewater treatment system and was cultured in pH ranged 3 to 11. High specific growth rate and removal rate of nitrogen and phosphorus were shown at pH 7 as $0.71day^{-1}$, 7.61 mg-N/L/day, and 1.24 mg-P/L/day, respectively. The specific growth rate examined with aeration rate between 0 and 2 vvm (vol/vol-min) highly presented as $1.2day^{-1}$ with 1.5 ~ 2 vvm, while the nitrogen removal rate was elevated with 0.5 vvm as 9.43 mg-N/L/day.

• 한국균학회지
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• 제23권3호통권74호
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• pp.275-283
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• 1995

The nutritional requirements of mycelial growth for Pleurotus spp. were studied. As the carbon sources, soluble starch and dextrin, nitrogen sources, arginine and ammonium tartrate, and calcium sources, $CaCO_3$ enhanced mycelial growth. Optimum C/N ratio was 100 : 1. On the base of results from the experiment on nutritional requirements, the following receipe is suggested for growth of Pleurotus spp.; starch 15 g, arginine 3.484 g, ammonium tartrate 3.06 g, $CaCO_3$ 0.314 g, $KH_2PO_4$ 8.138 g, $K_2HPO_4$ 1.584 g, $MgSO_4{\cdot}7H_2O$ 1.5 g for P. sajor-caju and 2.5 g for P. ostreatus. $FeSO_4{\cdot}7H_2O$ 0.02 g, $ZnSO_4{\cdot}7H_2O$ 0.03 g, $MnSO_4{\cdot}7H_2O$ 0.02 g, optimum pH 6.0. This new synthetic medium is tentatively designated as Park's medium.

• 생명과학회지
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• 제11권2호
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• pp.153-158
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• 2001

To investigate the effects of soil acidification on growth of Impatiens balsamina L. plants were transplanted to acidified soils with H$_2$SO$_4$ solution. The concentrations of soluble Ca, Mg, K, Al and Mn in the acidified soils increased with increment of H$^{+}$ addition to the soil. In both species, the plant height and root length were inhibited by soil acidification, showing much severer inhibition in Impatiens balsamina L. than in Tagetes patula L., As the soil pH decreases, the growth of underground parts decreased greatly than that of above ground parts in both species. Total dry weight decreased with increased Al concentration as well as lowered soil pH in both plants. There was a strong positive correlation between relative total dry weight and molar (Ca+Mg+K) / Al ratio of the soil. The results suggest that molar(Ca+Mg+K)/ Al ratio of the soil may be useful indicator for assessing the critical load of acid deposition in herb species.s.

• 생명과학회지
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• 제15권3호
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• pp.382-386
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• 2005

산성비가 식물 생장에 미치는 영향과 식물의 생화학적 방어반응을 조사하고자 봉선화를 이용하여 인공 산성비(pH 2.0, 3.0, 4.0, 5.6) 실험을 수행하였다. 산성비의 pH가 낮을수록 생육 피해는 심하게 나타났으며 pH 3.0 이하의 처리에 의해 잎에 암회색 또는 적갈색의 괴사반점이 생성되었다. MDA 함량은 pH 2.0 처리에서 약 $40\%$의 증가를 나타내었다. 산성비의 $H^+$ 부하량 증가에 따라 산화형인 DHA 및 GSSG의 함량이 증가하였다. 항산화효소인 SOD, APX, DHAR, GP등의 활성도 산성비의 $H^+$ 부하량의 증가에 따라 크게 증가하는 것으로 나타났다. 이상의 결과로 볼 때 산성비는 봉선화 식물에 활성산소 생성에 의한 산화스트레스를 일으키며, 이를 무독화하기 위해 식물의 생화학적 방어반응이 작용하는 것으로 사료된다

• 한국식품과학회지
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• 제28권5호
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• pp.987-993
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• 1996

본 연구에서는 Bifidobacterium을 우유와 두유에 접종하여 $37^{\circ}C$에서 발효 특성, 적정 발효 기간 및 효율적인 증식을 위한 생육 인자를 찾고자 하였다. 이를 위하여 pH, 산도, glucose함량, 생균수, ${\alpha}-galactosidase$활성 그리고 ${\beta}-galactosidase$활성 변화를 조사하였다. $37^{\circ}C$에서 일반 발효 특성을 측정했을 때 48시간동안 우유의 발효는 pH의 감소와 산 생성의 증가는 현저한 반면, 세포 증식을 24시간동안 증가하였으나 남은 24시간동안은 감소를 보였다. 또한 효소 반응은 ${\beta}-galactosidase$ 활성이 높은 반면, ${\alpha}-galactosidase$는 비교적 낮았으며 glucose 함량은 세포 증식기에 높았다. 두유의 경우는 우유에 비해 pH의 감소가 큰 반면 적정산도 증가는 비슷하였다. 세포 증식은 발효 2일동안 이루어졌으며, ${\alpha}-,\;{\beta}-galactosidase$ 모두 활성이 높게 나타났고, glucose 함량도 1일 동안 지속적인 증가를 나타냈다. 또한 적정 발효기간은 발효유는 24-36시간, 발효 두유는 약 24시간이 바람직한 것으로 나타났다. Bifidobacterium의 성장 촉진 인자의 영향을 발효 시간에 따른 pH와 생균수 변화로 조사한 결과, 두유에서는 fucosyllactose, 그리고 우유에서는 발효 초기에 L-cysteine·HCl, 발효 진행중에는 fucosyllactose가 효과적인 생육 인자로 작용하였다.

• 한국환경과학회지
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• 제5권5호
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• pp.611-617
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• 1996

유일한 탄소원으로서 Biphenyl을 포함하고 있는 액체배지에서 Pseudomonas sp. P2의 생육에 미치는 영양원의 효과에 관해 연구하였다. Pseudomonas sp. P2의 특성을 조사하기 위한, 배양시간은 균의 생육 유선에서 대수성장기 말인 100시간으로 하였다. PCBs를 분해하는 Pseudomonas sp. P2의 생육을 위한 최적 조성은 1000 mg/L $NH_4NO_3$, 1000 mg/L KH_2PO_4$, 100 mg/L MgSO_4$.$7H_2O$, 30 mg/L $CaCl_2$.$2H_2O$, 200 mg/L NaCl, 10mg/L $FeSO_4$.$7H_2O$였다. Pseudomonas sp. P2에 의한 100시간 배양후 절연유 내에 있는 PCBs의 분해률은 500mg/L에서 59.3%, 1000mg/L에서 57.6%, 1500mg/L에서 51.4%, 2000mg/L에서는 48.775 였다.