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Jeon, Che Ok,Park, Minjeong,Ro, Hyun-Su,Park, Woojun,Madsen, Eugene L. American Society for Microbiology 2006 Applied and environmental microbiology Vol.72 No.2
<B>ABSTRACT</B><P><I>Polaromonas naphthalenivorans</I> CJ2, found to be responsible for the degradation of naphthalene in situ at a coal tar waste-contaminated site (C.-O. Jeon et al., Proc. Natl. Acad. Sci. USA 100:13591-13596, 2003), is able to grow on mineral salts agar media with naphthalene as the sole carbon source. Beginning from a 484-bp <I>nagAc</I>-like region, we used a genome walking strategy to sequence genes encoding the entire naphthalene degradation pathway andadditional flanking regions. We found that the naphthalene catabolic genes in <I>P. naphthalenivorans</I> CJ2 were divided into one large and one small gene cluster, separated by an unknown distance. The large gene cluster (<I>nagRAaGHAbAcAdBFCQEDJI′ORF1tnpA</I>) is bounded by a LysR-type regulator (<I>nagR</I>). The small cluster (<I>nagR2ORF2I'KL</I>) is bounded by a MarR-type regulator (<I>nagR2</I>). The catabolic genes of <I>P. naphthalenivorans</I> CJ2 were homologous to many of those of <I>Ralstonia</I> U2, which uses the gentisate pathway to convert naphthalene to central metabolites. However, three open reading frames (<I>nagY</I>, <I>nagM</I>, and <I>nagN</I>), present in <I>Ralstonia</I> U2, were absent. Also, <I>P. naphthalenivorans</I> carries two copies of gentisate dioxygenase (<I>nagI</I>) with 77.4% DNA sequence identity to one another and 82% amino acid identity to their homologue in <I>Ralstonia</I> sp. strain U2. Investigation of the operons using reverse transcription PCR showed that each cluster was controlled independently by its respective promoter. Insertional inactivation and lacZ reporter assays showed that <I>nagR2</I> is a negative regulator and that expression of the small cluster is not induced by naphthalene, salicylate, or gentisate. Association of two putative <I>Azoarcus</I>-related transposases with the large cluster and one <I>Azoarcus</I>-related putative salicylate 5-hydroxylase gene (<I>ORF2</I>) in the small cluster suggests that mobile genetic elements were likely involved in creating the novel arrangement of catabolic and regulatory genes in <I>P. naphthalenivorans</I>.</P>
Jeon, Eugene,Hyeon, Jeong eun,Sung Eun, Lee,Park, Byeoung-Soo,Kim, Seung Woo,Lee, Jinwon,Han, Sung Ok Oxford University Press 2009 FEMS microbiology letters Vol.301 No.1
<P>In this study, Saccharomyces cerevisiae was engineered for simultaneous saccharification and fermentation of cellulose by the overexpression of the endoglucanase D (EngD) from Clostridium cellulovorans and the beta-glucosidase (Bgl1) from Saccharomycopsis fibuligera. To promote secretion of the two enzymes, the genes were fused to the secretion signal of the S. cerevisiaealpha mating factor gene. The recombinant developed yeast could produce ethanol through simultaneous production of sufficient extracellular endoglucanase and beta-glucosidase. When direct ethanol fermentation from 20 g L(-1)beta-glucan as a substrate was performed with our recombinant strains, the ethanol concentration reached 9.15 g L(-1) after 50 h of fermentation. The conversion ratio of ethanol from beta-glucan was 80.3% of the theoretical ethanol concentration produced from 20 g L(-1)beta-glucan. In conclusion, we have demonstrated the construction of a yeast strain capable of conversion of a cellulosic substrate to ethanol, representing significant progress towards the realization of processing of cellulosic biomass in a consolidated bioprocessing configuration.</P>
Eugene Jeon,Jeong-eun Hyeon,서동진,Young-Woong Suh,Seoung Wook Kim,송광호,Sung Ok Han 한국분자세포생물학회 2009 Molecules and cells Vol.28 No.4
Heterologous secretory expression of endoglucanase E (Clostridium thermocellum) and β-glucosidase 1 (Saccharomycopsis fibuligera) was achieved in Saccharomyces cerevisiae fermentation cultures as an α-mating factor signal peptide fusion, based on the native enzyme coding sequence. Ethanol production depends on simultaneous saccharification of cellulose to glucose and fermentation of glucose to ethanol by a recombinant yeast strain as a microbial biocatalyst. Recombinant yeast strain expressing endoglucanase and β-glucosidase was able to produce ethanol from β-glucan, CMC and acid swollen cellulose. This indicates that the resultant yeast strain of this study acts efficiently as a whole cell biocatalyst.
The Early Trauma Inventory Self Report-Short Form: Psychometric Properties of the Korean Version
JuRi Jeon,EunHo Lee,SunWoo Lee,Eugene Jeong,JiHae Kim,Dongsoo Lee,HongJin Jeon 대한신경정신의학회 2012 PSYCHIATRY INVESTIGATION Vol.9 No.3
Objective-Experiencing traumatic events in childhood is related to various psychiatric problems in adulthood, and a comprehensive tool for measuring childhood trauma is necessary in this field. This study aimed to examine the psychometric properties, and factor structure of the Korean version of the Early Trauma Inventory Self Report-Short Form (ETISR-SF). ETISR-SF measures the childhood trauma, including physical, and emotional sexual abuse, as well as general traumas. Methods-A clinical and nonclinical samples comprising of 97 subjects from a local community, and 207 patients with the ETISR-SF, were assessed. Other tools, including the Childhood Trauma Questionnaire-Short Form (CTQ-SF), the Beck Depression Inventory (BDI), and the Beck Anxiety Inventory (BAI) were used to assess clinical symptoms. Additional data from 69 college students was used to examine the test-retest reliability. Results-The original four-factor model was supported by the confirmatory factor analysis scale [χ2 (351, n=304)=3374.025, p<0.001, TLI=0.969, CFI=0.972, RMSEA=0.030]. The ETISR-SF was found to be a reliable instrument (Cronbach’s α=0.869). Comparison of the ETISR-SF scores discriminated the clinical group from that of the control group. The measure showed good convergent and divergent validity, in that the scores were correlated higher with the scores on the CTQ-SF (0.691) than with the scores on the BDI or BAI (0.424, 0.397 respectively). The ETISR-SF was found to be temporally stable, showing the moderate to high correlation (0.844). Conclusion-These findings suggest that the Korean version of the ETISR-SF appears to be a reliable and valid instrument for the measurement of reported childhood trauma.
Park, Minjeong,Jeon, Yeji,Jang, Ho Hee,Ro, Hyun-Su,Park, Woojun,Madsen, Eugene L.,Jeon, Che Ok American Society for Microbiology 2007 Applied and environmental microbiology Vol.73 No.16
<B>ABSTRACT</B><P>Prior research revealed that <I>Polaromonas naphthalenivorans</I> CJ2 carries and expresses genes encoding the gentisate metabolic pathway for naphthalene. These metabolic genes are split into two clusters, comprising <I>nagRAaGHAbAcAdBFCQEDJI</I>′-<I>orf1</I>-<I>tnpA</I> and <I>nagR2</I>-<I>orf2I</I>″<I>KL</I> (C. O. Jeon, M. Park, H. Ro, W. Park, and E. L. Madsen, Appl. Environ. Microbiol. 72:1086-1095, 2006). BLAST homology searches of sequences in GenBank indicated that the <I>orf2</I> gene from the small cluster likely encoded a salicylate 5-hydroxylase, presumed to catalyze the conversion of salicylate into gentisate. Here, we report physiological and genetic evidence that <I>orf2</I> does not encode salicylate 5-hydroxylase. Instead, we have found that <I>orf2</I> encodes 3-hydroxybenzoate 6-hydroxylase, the enzyme which catalyzes the NADH-dependent conversion of 3-hydroxybenzoate into gentisate. Accordingly, we have renamed <I>orf2 nagX</I>. After expression in <I>Escherichia coli</I>, the NagX enzyme had an approximate molecular mass of 43 kDa, as estimated by gel filtration, and was probably a monomeric protein. The enzyme was able to convert 3-hydroxybenzoate into gentisate without salicylate 5-hydroxylase activity. Like other 3-hydroxybenzoate 6-hydroxylases, NagX utilized both NADH and NADPH as electron donors and exhibited a yellowish color, indicative of a bound flavin adenine dinucleotide. An engineered mutant of <I>P. naphthalenivorans</I> CJ2 defective in <I>nagX</I> failed to grow on 3-hydroxybenzoate but grew normally on naphthalene. These results indicate that the previously described small catabolic cluster in strain CJ2 may be multifunctional and is essential for the degradation of 3-hydroxybenzoate. Because <I>nagX</I> and an adjacent MarR-type regulatory gene are both closely related to homologues in <I>Azoarcus</I> species, this study raises questions about horizontal gene transfer events that contribute to operon evolution.</P>
<i>J</i> - AND <i>H</i> -BAND IMAGING OF <i>AKARI</i> NORTH ECLIPTIC POLE SURVEY FIELD
Jeon, Yiseul,Im, Myungshin,Kang, Eugene,Lee, Hyung Mok,Matsuhara, Hideo IOP Publishing 2014 The Astrophysical journal Supplement series Vol.214 No.2
<P>We present the J- and H-band source catalog covering the AKARI North Ecliptic Pole field. Filling the gap between the optical data from other follow-up observations and mid-infrared (MIR) data from AKARI, our near-infrared (NIR) data provides contiguous wavelength coverage from optical to MIR. For the J- and H-band imaging, we used the FLoridA Multi-object Imaging Near-ir Grism Observational Spectrometer on the Kitt Peak National Observatory 2.1 m telescope covering a 5.1 deg(2) area down to a 5 sigma depth of similar to 21.6 mag and similar to 21.3 mag (AB) for the J and H bands with an astrometric accuracy of 0 ''.14 and 0 ''.17 for 1 sigma in R.A. and decl. directions, respectively. We detected 208,020 sources for the J band and 203,832 sources for the H band. This NIR data is being used for studies including the analysis of the physical properties of infrared sources such as stellar mass and photometric redshifts, and will be a valuable data set for various future missions.</P>
Development of real-time automatic sorting system for color PET recycling process
Youngjun Jeon,Sangwoo Um,Jaemin Yoo,Minseok Seo,Eugene Jeong,Woojin Seo,Daewon Kang,Hancheul Song,Kyung-Soo Kim,Soohyun Kim 제어로봇시스템학회 2020 제어로봇시스템학회 국제학술대회 논문집 Vol.2020 No.10
Pollution from discarded plastic has become a serious environmental problem. The Great Pacific garbage patch consisting of abandoned plastics is killing marine life. In addition, micro-plastics decomposed by solar UV radiation and waves can accumulate in the human body. Recycling plastic is accordingly a critical element of waste management. As part of the solution to this problem, factory automation in recycling plants to handle more waste faster is essential. The amount of reproduced raw plastics is proportional to the inlet speed of the plastics waste stream into a recycling process line. Furthermore, the quality of recycled products with reproduced raw plastics depends on the sorting purity through the line. Thus, an automated system should be capable of real-time classification of the plastics category and rapid manipulation for removing selected plastics. We propose a real-time sorting system for mixed color plastics by applying a machine learning algorithm and a parallel manipulator with a vacuum suction pad. The learning data and picking test samples were collected from a municipal waste disposal site at RM corporation factory. This work shows the feasibility of real-time plastics recycling automation and a future development direction.