• Journal of the Korean Institute of Telematics and Electronics B
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• v.33B no.2
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• pp.209-216
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• 1996

This paper deals with the speed control of the switched reluctnace motor using fuzzy PI controller. A fuzzy logic control provides a good approach to nonlinear system because it does not require a detailed mathematical model to formulate the algorithm. The fuzzy PI controller is implemented by MCS80C196KB, a 16 bit one-chip microcontroller, and an EPROM is used for the commutation logic of the SRM. The simulation and experimental results show that the performance of the fuzzy PI controller is superior to that of the conventional PI controller in terms of response time, settling time and overshoot. In particular, the robustness of the system is largely improved.

• Journal of the Korean Institute of Telematics and Electronics B
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• v.33B no.2
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• pp.217-226
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• 1996

Switched reluctance motor (SRM) drives appear today as viable alternatives to induction and brushless motor drives in a wide range of application such as machine tools, fans, and pumps. This paper deals with a new converter topology which can be used in order converter. The split source type converter consists of minimum switching devices to be used in switched reluctance motor (SRM) drive. In this proposed converter two switches and six diodes are added to split source type converter. The proposed converter has performance minimizes the negative torque, Which puts the phase current off by double impressed voltages. The major advangtage of this converter is the increase of the average output power while improving better converter efficiency in heavy load and high speed than other topologies. The proposed converter system has been implemented using 80C196KB microcontroller and experiments were carried out ot verify the simulation results.

• Asian-Australasian Journal of Animal Sciences
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• v.15 no.8
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• pp.1071-1075
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• 2002

In order to identify and develop the specific DNA marker for the identification of Hanwoo (Korean Cattle) from other breeds, a specific DNA marker of 519 bp was identified and sequenced from polymorphic analysis using RAPD-PCR for 6 cattle breeds. Two different repetitive sequences, $(AAC)_5$ and $(GAAGA)_2$, were selected and designed to use specific probe to develop a DNA marker for Hanwoo specific. When the $(AAC)_5$ probe was applied, the 10 kb specific DNA marker showed in the DNA fingerprinting from 237 of 281 Hanwoo individuals. This novel Hanwoo specific DNA probe is useful to perform the marker-assisted selection for screening Hanwoo purity as an unique genetic source.

• KSBB Journal
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• v.8 no.2
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• pp.104-109
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• 1993

A vector for plant transformation which had two reporter genes(Gus and Hpt genes) in a single plasmid was constructed. After rice embryos imbibed DNA solution, DNA uptake and gene expression in rice were monitored. Main expression sites of the Gus gene were meristem of root and coleoptiles. There was no difference in Hpt gene expression between a single Hpt vector and the constructed vector in viability of rice in the hygromycin medium after DNA imbibition, The genomic DNA and total RNA extracted from rice transformant survived in the hygromycin medium were subjected to PCR and RT PCR analysis, respectively. As a result, we found the existence of the Hpt gene and its expression in rice.

• The Transactions of the Korean Institute of Electrical Engineers
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• v.39 no.2
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• pp.119-132
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• 1990

To design protection coordination for an electric power distribution system, an expert system is developed, using both the veteran expert's heuristics and the guide book for the distribution facility operation considering feeder configuration, service route, load characteristics fault current and load current. The expert system developed in this papaer determines the type of protective device(clearing current and sequence). The location and rating change of protective device in the old feeder is realized by using old database. Current(T-C) curves of various kinds of protective devices are stored in Knowledge Base (KB). The expert system is developed on a 32 bit personal computer using PROLOG, AutoCAD,dBASEIIIPLUS and FORTRAN. To compute the fault current and loadflow, FORTRAN is used.

• Electronics and Telecommunications Trends
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• v.26 no.2
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• pp.33-41
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• 2011

모바일 단말 전자결제서비스는 이동전화단말에서 신용카드 등 금융서비스를 제공하는 것을 의미한다. 그러나 모바일 단말 전자결제는 서비스 종류 및 인프라 한계로 활성화되지 못하고 있는 상황이다. 모바일 단말 금융결제를 위해서는 RFID 기반 USIM, 단말, 결제기가 필요한데, 현재 RFID 기반 금융 USIM 용량제한(144KB)으로 서비스 확장이 곤란하며 특히 인프라(단말, 결제기 등) 구축이 미흡한 상황이다. 모바일 단말 금융결제 활성화를 위해서는 이동통신사 USIM을 국제규격인 NFC로 표준화, 범용성 및 규모의 경제 확보, 모든 국산단말에서 금융결제가 가능하도록 콤비 또는 NFC 등 RF 기능 탑재의무화, 전국에 보급된 카드결제기에 RF 탑재 추진 등이 필요하다. 본 고에서는 모바일 단말 전자결제서비스의 활성화 방안을 제시하고 이의 기대효과를 분석한다.

• Proceedings of the Korea Concrete Institute Conference
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• 1990.10a
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• pp.151-156
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• 1990

This is an experimental study to investigate chante of early strength of polymer concrete due to curing temperature change. Polymer binders that were used in the experiment include 2 types of epoxy system and 4 types of polyester system which are commercially producer in Korea. The study result showed that there was a difference in early strength by curing temperature. At $35^{\circ}C$ which is a higher than normal curing temperature, higher strengths were developed in polymer concretes prepared with KB-Clear and YD-128 of epoxy system, and G-550 and H-660 of polyester system. However, at the same temperature, reduced strengths were obtained for FH-103 and TR-132 of polyester system. Further study under various curing conditions with humidity and temperature change will warrant more generalized result.

• The Korean Journal of Food And Nutrition
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• v.6 no.4
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• pp.314-321
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• 1993

We have cloned the Bacillus cellulyticus K-12 avicelase (Avi, E.C.3.2.1.4) gene (ace A) In E. coli. This was accompanied by using the vector PT7T3U 19 and Hind W -Hind m libraries of Bacillus cellulyticus K-12 chromosomal inserts created in 5.cofi. The Libraries were screened for the expression of avicelase by monitoring the immunoreaction of the anti-avicelase (immunoscreening). Positive clones (Ac-3, Ac-5, and Ac-7) contained the identical 3.5kb Hind III fragment as determined by restriction mapping and Southern hybridization, and expressed avicelase efficiently and constituvely using its own promoter in the heterologous host. From the immunoblotting analysis, a polypeptide which showed a CMCase activity with an Mr of 54000 was detected.

• Journal of Animal Science and Technology
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• v.63 no.5
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• pp.1204-1206
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• 2021

Limosilactobacillus fermentum JN2019, formerly named Lactobacillus fermentum JN2019, was isolated from kimchi. Its genome was completely sequenced using the PacBio RSII sequencing system to explore beneficial phenotypes. In a previous study, L. fermentum JN2019 was used to ferment the by-product of tumeric for use in livestock feed. The 2.3 Mb genome had a high guanine (G) + cytosine (C) content of 50.6% and a 30 kb plasmid. The data will inform the comprehensive understanding of JN2019 and provide insights for potential applications.

• Journal of Embryo Transfer
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• v.33 no.4
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• pp.195-203
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• 2018

Interferon-tau (IFNT) is known as a major conceptus protein that signals the process of maternal recognition of pregnancy in ruminants. Also, multiple interferon genes exist in cattle, However, molecular mechanisms of these bovine IFNT (bIFNT) genes whose expressions are limited have not been characterized. We and others have observed that expression levels of bovine subtype IFNT genes in the tissues of ruminants; thus, bIFNT1 and other new type I (bIFNTc1/c2/c3) gene co-exist during the early stages of conceptus development and non-trophoblast cells. Its genes transcription could be regulated through CDX2 and ETS2 and JUN and/or cAMP-response element binding protein (CREB)-binding protein (CREBBP) expression, a transcription factor implicated in the control of cell differentiation in the trophectoderm. Bovine ear-derived fibroblast cells, were co-transfected with luciferase reporter constructs carrying upstream (positions -1000 to +51) regions of bIFNT1 and other new type I gene and various transcription factor expression plasmids. Compared to each - 1kb-bIFNT1/c1/c2/c3-Luc increased when this constructs were co-transfected with CDX2, ETS2, JUN and/or CREBBP. Also, Its genes was had very effect on activity by CDX2, either alone or with the other transcription factors, markedly increased luciferase activity. However, the degree of transcriptional activation of the bIFNTc1 gene was not similar to that bIFNT1/c2/c3 gene by expression plasmid. Furthermore, Sequence analyses also revealed that the expression levels of bIFNT1/c2/c3 gene mRNAs expression were highest on day 17, 20 and 22 trophoblast and, Madin-Darby bovine kidney (MDBK), Bovine ear-derived fibroblast (EF), and endometrium (Endo) non-trophoblast cells. But, bIFNTc1 mRNA had not same expression level, bIFNTc1 lowest levels than those of IFNT1/c2/c3 gene in both trophoblast and non-trophoblast cells. These results demonstrate that bovine subtype bIFNT genes display differential, in the trophoblast and non-trophoblast cells.