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DEVELOPMENT OF THE EPIDIDYMIS IN MEISHAN BOARS
Harayama, H.,Nanjo, I.,Kanda, S.,Kato, S. Asian Australasian Association of Animal Productio 1992 Animal Bioscience Vol.5 No.1
The developmental process of the epididymis was investigated in Meishan boars from 1 to 364 days of age. Epididymal weight increased rapidly between 45 and 150-180 days of age. The diameter and epithelial area of the epididymal ducts greatly increased up to 105-120 days of age. At 1 day of age, the central and distal cauda already had a pseudostratified epithelium surrounded by smooth muscle. At 60-75 days of age, the central and distal caput, corpus, and proximal cauda revealed a well-developed structure of the epithelium. The proximal caput showed a tall, irregular and vacuolar epithelium at 105-120 days of age. PAS-positive contents in the lumen of the caput, corpus and cauda epididymides were first detected at 60-75, 45-60 and 1-30 days of age, respectively. Moreover, in the central and distal caput, PAS-positive granules appeared at 60-75 days of age, and increased until 105-120 days. These results suggest that the epididymis develops completely by approximately 120 days of age, though its weight increases rapidly up to 150-180 days. Thus, it appears that development of the epididymis occurs at an earlier age in Meishan boars than in European and American breeds.
Hiroshi, Harayama,Seishiro, Kato Asian Australasian Association of Animal Productio 2001 Animal Bioscience Vol.14 No.8
In boar spermatozoa, the head-to-head agglutinability changes in parallel with the development of the fertilizing ability. Namely, both abilities gradually increase in the distal caput and corpus epididymides, but are subsequently suppressed in the cauda epididymidis. It has been postulated that these changes of the agglutinability are controlled via sperm interaction with specific epididymal plasma factors including agglutination mediators (agglutinins) and inhibitors (anti-agglutinins). Expression of these abilities (sperm agglutination and capacitation) is hardly observed in spermatozoa immediately. after ejaculation, but it occurs during incubation in a capacitation medium. Recently, we have purified and characterized epididymal plasma anti-agglutinin for boar spermatozoa. Moreover, we have conducted a series of experiments to reveal biological significance and mechanism of the head-to-head agglutination and have accumulated data indicating that boar sperm agglutination is mediated by capacitation-supporting factors including calcium, bicarbonate and sterol acceptors. This review introduces our recent data and discusses a possible mechanism for suppression of the agglutinability in the distal epididymidis and relationship between agglutinability and fertilizing ability.
Vibration Minimized Design of Trapezoidal Acceleration Input for Semiconductor Manufacturing Systems
Mitsuo Hirata,Tomohiro Harayama,Kouji Yoshida,Youzou Fukagawa 제어로봇시스템학회 2009 제어로봇시스템학회 국제학술대회 논문집 Vol.2009 No.8
In this paper, we discuss about the design of the trapezoidal acceleration input which does not excite the mechanical vibration modes. We first obtain the spectrum of the trapezoidal acceleration input analytically, and the frequencies where the spectrum becomes zero are obtained. Since the zero spectrum frequencies are the function of the ramp-up and ramp-down time, they can be determined so as to coincide with the resonance frequencies of the mechanical vibration modes. The effectiveness of the proposed method is evaluated by simulations. The proposed method is very simple, and it is easy to apply not only to the stepper for semiconductor manufacturing systems but also to any other industrial systems that use trapezoidal acceleration input.
Identification of Novel Non-Metal Haloperoxidases from the Marine Metagenome
( Hui Jeong Gwon ),( Ide Teruhiko ),( Harayama Shigeaki ),( Sang Ho Baik ) 한국미생물 · 생명공학회 2014 Journal of microbiology and biotechnology Vol.24 No.6
Haloperoxidase (HPO, E.C.1.11.1.7) is a metal-containing enzyme oxidizing halonium species, which can be used in the synthesis of halogenated organic compounds, for instance in the production of antimicrobial agents, cosmetics, etc., in the presence of halides and H2O2. To isolate and evaluate a novel non-metal HPO using a culture-independent method, a cassette PCR library was constructed from marine seawater in Japan. We first isolated a novel HPO gene from Pseudomonas putida ATCC11172 by PCR for constructing the chimeric HPO library (HPO11172). HPO11172 showed each single open-reading frame of 828 base pairs coding for 276 amino acids, respectively, and showed 87% similarity with P. putida IF-3 sequences. Approximately 600 transformants screened for chimeric genes between P. putida ATCC11173 and HPO central fragments were able to identify 113 active clones. Among them, we finally isolated 20 novel HPO genes. Sequence analyses of the obtained 20 clones showed higher homology genes with P. putida or Sinorhizobium or Streptomyces strains. Although the HPO A9 clone showed the lowest homology with HPO11172, clones in group B, including CS19, showed a relatively higher homology of 80%, with 70% identy. E. coli cells expressing these HPO chimeric genes were able to successfully bioconvert chlorodimedone with KBr or KCl as substrate.