• 제목/요약/키워드: Rh

검색결과 2,737건 처리시간 0.034초

Rhizobium sp. RH84에 의한 간척지 환경에서의 헤어리베치 생육촉진 (Hairy Vetch Growth-Promoting Rhizobium sp. RH84 and Application to Reclaimed Land)

  • 장종옥;권미경;박동진;성창근;김창진
    • Journal of Applied Biological Chemistry
    • /
    • 제56권4호
    • /
    • pp.235-239
    • /
    • 2013
  • 녹비 작물인 헤어리베치의 간척지 적용을 위해 본 연구에서는 헤어리베치의 뿌리혹으로부터 분리 된 Rhizobium sp. RH84의 특성을 파악하고 이를 직접 간척지에 적용하여 헤어리베치의 생산량 증대에 이용하고자 하였다. 전보에서 분리 한 RH84의 형태학적, 생리학적 특성 및 식물생육촉진(PGP) 활성을 확인하기 위하여 옥신, 질소 고정능, 인산 가용능, sideropore 생산능을 분석하였다. 그 결과, RH84는 식물호르몬인 IAA를 $9.03{\mu}g/mL$ 생산하였고, 질소 고정 활성을 가진 균주이었다. 또한 염 농도가 0.3%인 간척지 토양에서의 헤어리베치 생장에 영향을 주며, 간척지 포장에서 약 56%의 헤어리베치 수확량을 증가시켰다. 따라서 Rhizobium sp. RH84 균주는 염 농도가 높은 간척지에서 녹비작물인 헤어리베치의 생장을 촉진시키며 수확량을 증가시키기 위한 균주임을 확인하였다.

홍삼유래 ginsenosides Rh1의 단핵구 U937 세포 유착조절 효과 (Regulatory Effect of Ginsenosides Rh1 on Monocytic U937 Cell Adhesion)

  • 김병훈;조재열
    • Journal of Ginseng Research
    • /
    • 제33권4호
    • /
    • pp.324-329
    • /
    • 2009
  • G-Rh1에 의한 단핵구 세포주인 U937 세포의 유착조절 능을 조사하여 다음과 같은 결론을 얻었다. 1. G-Rh1은 CD29 항체 (MEM101A) 처리에 의해 유도된 세포-세포간 유착현상을 유의적으로 억제하였다. 2. G-Rh1은 fibronectin처리에 의해 유도된 U937 세포-fibronectin간 유착현상을 유의적으로 억제하였다. 3. G-Rh1은 CD29의 세포표면 발현 수준을 유의적으로 감소시켰다. 최근 활발히 G-Rh1의 약리작용 연구들이 진행되고 있다. 특별히, 본 화합물은 항알러지, 피부염증질환 치료효과, 항암효과 및 여성호르몬 유사기능 등이 있는 것으로 보고된 바있다. CD29-매개성 세포유착과정이 다양한 염증과정, 알러지 반응 및 암세포의 이동 및 전이성과 관련이 있다는 관점에서 볼 때 본 연구결과는 이들 약물이 갖는 치료기전의 하나가 CD29 기능저해에서 비롯될 수 있음을 제시한다고 하겠다. 이후 G-Rh1의 억제 기능에 관한 기전 이해를 위해 세포유착 유도 신호전달 단백질의 활성을 포함한 다양한 분자적 수준에서의 추가적인 실험들을 진행하고 한다.

E. coli 발현 시스템에 의해 생산된 recombinant human bone morphogenetic protein-2의 정제와 생물학적 활성 (Purification and biological activity of recombinant human bone morphogenetic protein-2 produced by E. coli expression system)

  • 최경희;문금옥;김수홍;윤정호;장경립;조규성
    • Journal of Periodontal and Implant Science
    • /
    • 제38권1호
    • /
    • pp.41-50
    • /
    • 2008
  • Purpose: Bone morphogenetic protein-2(BMP-2) has been shown to possess significant osteoinducitve potential. There have been attempts to overcome a limitation of mass production, and economical efficiency of BMP. The aim of this study was to produce recombinant human BMP-2(rhBMP-2) from E. coli in a large scale and evaluate its biological activity. Materials and Methods: The E.coli strain BL21(DE3) was used as a host for rhBMP-2 production. Dimerized rhBMP-2 was purified by affinity chromatography using Heparin column. To determine the physicochemical properties of the rhBMP-2 expressed in E. coli, we examined the HPLC profile and performed Western blot analysis. The effect of the purified rhBMP-2 dimer on osteoblast differentiation was examined by alkaline phosphatase (ALP) activity and representing morphological change using C2C12 cell. Results: E. coli was genetically engineered to produce rhBMP-2 in a non-active aggregated form. We have established a method which involves refolding and purifying a folded rhBMP-2 dimer from non-active aggregates. The purified rhBMP-2 homodimer was characterized by SDS-PAGE as molecular weight of about 28kDa and eluted at 34% acetonitrile, 13.27 min(retention time) in the HPLC profile and detected at Western blot. The purified rhBMP-2 dimer stimulated ALP activity and induced the transformation from myogenic differentiation to osteogenic differentiation. Conclusion: rhBMP-2 was produced in E. coli using genetic engineering. The purified rhBMP-2 dimer stimulated ALP activity and induced the osteogenic differentiation of C2C12 cells.

한우에 Ov-synch 처리시 배란시기와 수태율 구명에 관한 연구 (Synchronization Rate, Size of the Ovulatory Follicle, and Pregnancy Rate after Synchronization of Ovulation Method in Hanwoo)

  • 박정준;이명식;박수봉;임석기;전기준;정영훈;우제석;나기준;고대환
    • 한국수정란이식학회지
    • /
    • 제18권3호
    • /
    • pp.187-193
    • /
    • 2003
  • 본 연구는 한우에 GnRH + PGF$_2$$\alpha$+GnRH (Ov-synch)를 처리하여 배란동기화를 시켰으며, 2차 GnRH 투여후 배란시간, 수태율, 계절별 수태율, 산차별 수태율을 조사하였으며, 시험축은 2산 이상의 개체를 무작위로 선발하여 실험에 공시하였으며, 배란동기화 처리후 1회 인공수정을 실시하고 수태율을 환산하였다. 호르몬 처리방법으로는 GnRH + PGF$_2$$\alpha$ + Gn-RH(Ov-synch)법을 이용하였으며, 배란시간의 조사는 초음파를 이용하여 2차 GnRH 투여 후 24시간부터 31시간까지 2시간 간격으로 난소를 촬영하여 배란 여부를 조사하였다. 1. 배란동기화 처리후 24시간부터 31시간까지 2시간 간격으로 난소의 상태를 확인한 결과 28∼30시간 사이에 80%(20/25)로 가장 많이 배란된 것으로 나타났다. 2. 수태율에 있어서는 계통별 1회 수정 수태율은 고급육 계통이 48.1%(38/79)로 다소 높게 나타났다. 3. 산차에 따른 수태율은 1∼2, 3∼4산차에서 각각 44.3, 55%로 나타났다. 4. 계절별로는 여름보다는 봄과 가을에서 47.3%로 다소 높은 경향이였다.

프로바이틱스 Lactobacillus helveticus와 Pediococcus pentosaceus의 조합에 의한 진세노사이드의 발효적 형질전환 (Fermentative transformation of ginsenosides by a combination of probiotic Lactobacillus helveticus and Pediococcus pentosaceus)

  • ;;김진만;양승환
    • 미생물학회지
    • /
    • 제54권4호
    • /
    • pp.436-441
    • /
    • 2018
  • 인삼은 우수한 약리 활성 작용을 보이는 전통적인 약초이다. 본 연구에는 프로바이오틱스 Lactobacillus helveticus KII13과 Pediococcus pentosaceus KID7 균주를 진세노사이드(ginsenoside) 함량을 증가시키기 위해 조 인삼 추출물을 발효시켜 진세노사이드를 형질전환 시키는데 사용되었다. 발효삼 추출물의 TLC(Thin-layer chromatography) 분석 결과, 5일간의 발효 후 주요 사포닌인 진세노사이드 Rg3, Rh1 및 Rh2로 변환되는 것으로 나타났다. HPLC 분석을 수행하여 주요 및 미량 진 세노사이드를 정량화하였다. 3일째에는 Rg3가 나타나고, 5일째에는 Rh2 및 Rh1이 나타난다. L. helveticus KII13과 P. pentosaceus KID7의 공동 배양은 주요 진세노사이드(Rb1과 Rg1)를 미량 진세노사이드(Rg3, Rh2, Rh1)로 전환시키는 것을 학인하였다.

Autocrine Regulation of Gonadotropin-releasing Hormone (GnRH) Operates at Multiple Control levels of GnRH Gene Expression in GT1-1 Neuronal Cells

  • Jin Han;Sehyung Cho;Woong Sun;Kyungjin Kim
    • Animal cells and systems
    • /
    • 제2권4호
    • /
    • pp.483-488
    • /
    • 1998
  • We previously found that a potent gonadotropin-releasing hormone (GnRH) agonist, buserelin, decreases GnRH promoter activity together with GnRH mRNA level, providing evidence for an autoregulatory mechanism operating at the level of GnRH gene transcription in immortalized GT1-1 neuronal cells. To examine whether agonist-induced decrease in GnRH mRNA level requires the continuous presence of buserelin, we performed a pulse-chase experiment of buserelin treatment. Short-term exposure (15 min) of GT1-1 neuronal cells to buserelin ($10{\mu}M$) was able to decrease GnRH mRNA levels when determined 24 h later. When GT1-1 cells were treated with buserelin ( $10{\mu}M$) for 30 min and then incubated for 1, 3, 6, 12, 24, and 48 h after buserelin removal, a significant decrease in GnRH mRNA levels was observed after the 12 h incubation period. These data indicate that inhibitory signaling upon buserelin treatment may occur rapidly, but requires a long time (at least 12 h) to significantly decrease the GnRH mRNA level. To examine the possible involvement of de novo synthesis and/or mRNA stability in buserelin-induced decrease in GnRH gene expression, actinomycin D ($5{\mu}m/ml$), a potent RNA synthesis blocker, was co-treated with buserelin. Actinomycin D alone failed to alter basal GnRH mRNA Revel, but blocked the buserelin-induced decrease in GnRH mRNA level at 12 h of post-treatment. These data suggest that buserelin may exert its inhibitory action by altering the stability of GnRH mRNA. Moreover, a polvsomal RNA separation by sucrose gradient centrifugation demonstrated that buserelin decreased the translational efficiency of the transcribed GnRH mRNA. Taken together, these results clearly indicate that GnRH agonist buserelin acts as an inhibitory signal at multiple levels such as transcription mRNA stability, and translation.

  • PDF

Hypophyseal and Gonadal Response to GnRH in Buffalo Heifers (Bubalus bubalis)

  • Singh, C.;Madan, M.L.
    • Asian-Australasian Journal of Animal Sciences
    • /
    • 제11권4호
    • /
    • pp.416-421
    • /
    • 1998
  • The objective of this study was to investigate the responsiveness of hypophysis and gonads to synthetic GnRH among noncycling Murrah buffalo heifers at 24 months of age. The plasma FSH, LH, estradiol and progesterone levels were measured in blood samples collected at 1 hour before and upto 18th day subsequent to the administration of GnRH ($(200 {\mu}g)$) or saline (2 ml). The pretreatment levels of plasma FSH, LH estradiol and progesterone among GnRH treated heifers (N = 6) were $11.55{\pm}0.57ng/ml$, $0.68{\pm}0.06ng/ml$, $19.84{\pm}0.82pg/ml$ and $0.45{\pm}0.07ng/ml$ respectively. A quick elevation of FSH (p < 0.01) and LH (p < 0.05) within 5 min of GnRH administration was observed in all the heifers. The peak FSH ($74.97{\pm}18.63ng/ml$) and LH ($3.09{\pm}0.54ng/ml$) level was obtained at 30 min of GnRH administration. The elevated level of plasma estradiol on 5th to 18th day, FSH on 7th to 9th day (n = 3) and the progesterone on 13th to 18th day (n = 2) of GnRH injection was obtained. The study indicates that gonads of buffalo heifers at 24 months of age are responsive of GnRH induced gonadotropin release for folliculogenesis and luteal tissue formation

에너지 전환에 의한 동축 섬광관 펌핑 Rhodamine 6G 색소 레이저의 출력 증가 (Output Enhancement of Coaxial Flashlamp Pumped Rhodamine 6G Dye Laser by Energy Transfer)

  • 장우권
    • 한국광학회지
    • /
    • 제4권2호
    • /
    • pp.195-199
    • /
    • 1993
  • Rh-6G(Rhodamine 6G)를 주색소로 하고 C-545(Coumarin 545)를 첨가색소로 하는 펄스형 혼합 색소레이저의 출력을 조사하였다. 동축형의 섬광관을 펌핑 광원으로 이용하였으며 Rh-6G 단일 색소로 발진할 경우 전기 입력 에너지가 346 J 일 때 첨두 출력과 에너지는 각각 27kW, 59mJ이었다. Rh-6G의 흡수 스펙트럼과 일치하는 형광 스펙트럼을 갖는 C-545를 에서지 주개로 선택하였다. Rh-6G의 농도를 최적 농도인 $1{\times}10_-4mol/l$로 고정하고 C-545의 농도를 $1{\times}10_7mol/l$부터 변화시키면서 혼합 색소에 대한 레이저의 출력 특성을 조사하였다. C-545의 농도가 Rh-6G 농도의 0.4%일 때 출력 에너지는 약 70% 증가하였다.

  • PDF

전기분해와 UV 조사에 의한 수중 Rhodamine B의 제거(II) (Removal of Rhodamine B in Water by Ultraviolet Radiation Combined with Electrolysis(II))

  • 김동석;박영식
    • 한국환경과학회지
    • /
    • 제18권6호
    • /
    • pp.667-674
    • /
    • 2009
  • This study has carried out to evaluate the effect of NaCI as electrolyte of single (electrolysis and UV process) and complex (electrolysis/UV) processes for the purpose of removal and mineralization of Rhodamine B (RhB) dye in water. It also evaluated the synergetic effect on the combination of electrolysis and UV process. The experimental results showed that RhB removal of UV process was decreased with increase of NaCl, while RhB removal of electrolysis and electrolysis/UV process was increased with increase of NaCI. The decolorization rate of the RhB solution in every process was more rapid than the mineralization rate identified by COD removal. The latter took longer time for further oxidation. Absorption spectra of an aqueous solution containing RhB showed a continued diminution of the RhB concentration in the bulk solution: concomitantly, no new absorption peaks appeared. This confirmed the decolorization of RhB, i.e., the breakup of the chromophores. It was observed that RhB removal in electrolysis/UV process is similar to the sum of the UV and electrolysis. However, it was found that the COD of RhB could be degraded more efficiently by the electrolysis/UV process than the sum of the two individual process. A synergetic effect was demonstrated in electrolysis/UV process.

RhPt 이종금속 나노입자의 크기 및 조성 제어를 통한 촉매 활성도에 관한 연구 (Investigation of Catalytic Activity Through Controlling Its Size and Composition of RhPt Bimetallic Nanoparticles)

  • 박정영;김선미
    • 한국분말재료학회지
    • /
    • 제18권6호
    • /
    • pp.538-545
    • /
    • 2011
  • This study shows that catalytic activity of bimetallic RhPt nanoparticle arrays under CO oxidation can be tuned by varying the size and composition of nanoparticles. The tuning of size of RhPt nanoparticles was achieved by changing concentration of rhodium and platinum precursors in one-step polyol synthesis. Two-dimensional RhPt bimetallic nanoparticle arrays in different size and composition were prepared through Langmuir-Blodgett thin film technique. CO oxidation was carried out on these two-dimensional nanoparticle arrays, revealing higher activity on the smaller nanoparticles compared to the bigger nanoparticles. X-ray photoelectron spectroscopy (XPS) results indicate the preferential surface segregation of Rh compared to Pt on the smaller nanoparticles, which is consistent with the thermodynamic analysis. Because the catalytic activity is associated with differences in the rates of $O_2$ dissociative adsorption between Pt and Rh, this paper suppose that the surface segregation of Rh on the smaller bimetallic nanoparticles is responsible for the higher catalytic activity in CO oxidation. This result suggests a control mechanism of catalytic activity via synthetic approaches of colloid nanoparticles, with possible application in rational design of nanocatalysts.