http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
수원 일월저수지에서 Microcystis aeruginosa (K$\ddot{u}$tzing) K$\ddot{u}$tzing 수화현상 시 환경요인들의 변화
김지은,박정원,조기안,김시균,Kim, Ji-Eun,Park, Jung-Won,Jo, Ki-An,Kim, Si-Kyoon 한국하천호수학회 2013 생태와 환경 Vol.46 No.2
본 연구는 수원 일월저수지에서 수화현상 시 환경요인들의 변화와 한국형 부영양화 지수를 이용하여 영양단계를 평가하였다. 수화현상 종은 남조류의 Microcystis aeruginosa Kutz.였으며 조사기간 내내 우점하였다. 수온은 평균 $25.7{\sim}28.4^{\circ}C$, pH는 8.4~11.17, CODcr는 4.25~$72.0mg\;L^{-1}$, 전기전도도는 333.1~$749.0{\mu}S\;cm^{-1}$, Chl-a는 22.0~$185.0mg\;L^{-1}$였다. 정체 수역인 정점 2에서 CODcr는 다른 정점에 비해 2.9배 정도로 높아 내부기원 유기물의 기여도가 높은 것으로 판단된다. 영양염인 TN은 평균 28.86~$56.75mg\;L^{-1}$, TP는 0.2~$1.24mg\;L^{-1}$로 매우 높았고, Fe는 0.11~$1.05mg\;L^{-1}$이었고, Si는 3.13~$7.46mg\;L^{-1}$이었다. TN과 TP는 일월저수지 내에 지속적으로 누적된 것으로 파악되었고, Fe도 높은 농도가 유지되었다. 한국형 부영양화지수는 37.19~147.22였다. 영양단계는 중영양에서 과영양 단계로 평가되었고, 같은 저수지 내에서도 시기 및 지점에 따라 영양단계가 다름을 나타내므로 많은 자료가 추적된다면 한국형 영양단계 분석은 저수지의 영양단계 분석 시 매우 유용하게 활용될 것으로 판단된다. Variances in environmental factors were followed in Ilwol reservoir, Suwon, during bloom of Microcystis aeruginosa (K$\ddot{u}$tzing) K$\ddot{u}$tzing, Cyanophtya from August to October, 2011. M. aeruginosa dominated the water column throughout the investigation period. The water temperature varied from $25.7^{\circ}C$ to $28.4^{\circ}C$, pH 8.40 to 11.17, CODcr 4.25 to $72.00mg\;L^{-1}$, electrical conductivity 333.1 to $749.0{\mu}g\;cm^{-1}$, and Chl-a 22 to $185mg\;L^{-1}$. In particular, the high levels of CODcr is likely indicate high contribution of autochthonous organic matters in the reservoir. TN varied from 28.86 to $56.75mg\;L^{-1}$, TP 0.20 to $1.24mg\;L^{-1}$, Fe 0.11 to $1.05mg\;L^{-1}$, and Si 3.13 to $7.46mg\;L^{-1}$. These increases imply constant accumulation in Ilwol reservior, and reinforce the idea of autochthonous organic matters input in the reservoir. The Korea Trophic Status Index ($TSI_KO$) varied from 37.19 to 147.22. Trophic levels varied from mesotrophic to hypertrophic level, and differed spatio-temporally. Therefore, it is concluded that $TSI_KO$ is useful for analyzing trophic status of reservoirs.
Selection of differential chirality of (R)- and (S)-3-hydroxybutyryl-CoA dehydrogenases
김지은,김경진 한국구조생물학회 2014 Biodesign Vol.2 No.4
(R)- and (S)-3-hydroxybutyryl-CoA dehydrogenases from Ralstonia eutropha H16 play a significant role in the biosynthesisof bioplastics and biofuels. (R)-3-hydroxybutyryl-CoA dehydrogenase (RePhaB) is an enzyme that is involved in thesynthetic pathway of polyalkanoates (PHA) which are used to make bioplastics, implant biomaterials, and biofuel. Whereas,(S)-3-hydroxybutyryl-CoA dehydrogenase (RePaaH1) is an enzyme that is involved in the biosynthesis of the n-butanol. Although both these enzymes utilize Acetoacetyl-CoA as a substrate to produce 3-hydroxybutyryl-CoA, the chirality ofthe final product is different—(R)-3-hydroxybutyryl-CoA by RePhaB and (S)-3-hydroxybutyryl-CoA by RePaaH1. Crystalstructures of RePhaB and RePaaH1 show remarkable differences in their structures, oligomeric states, and cofactorspecificity. RePhaB forms a tetramer, whereas RePaaH1 forms a dimer. Their cofactor requirements are also different—NADPH and NADH for RePhaB and RePaaH1, respectively. Moreover, their substrate binding modes are also substantiallydifferent. Interestingly, both enzymes undergo a conformational change upon binding to acetoaceryl-CoA substrate. InRePhaB, the lid-domain undergoes a large conformational change of about 4.6 Å to form a substrate pocket, whereas onlya small structural change is observed in RePaaH1. Comparison of active sites of these enzymes reveals the differences inthe position of catalytic residues, which ultimately determines the differential chirality of their products.