• 제목/요약/키워드: $GT_1$

검색결과 524건 처리시간 0.025초

연초의 적심방법이 품질구성형질에 미치는 영향 (Effect of Topping Method on the Quality Components of Flue-cured Tobacco)

  • 이종두;한종구;반유선;이정덕
    • 한국작물학회지
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    • 제33권1호
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    • pp.23-30
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    • 1988
  • 본 시험은 연초의 생육작황에 따라서 적심시기와 정도를 두어 처리하였을 때 잎담배의 품질형질에 미치는 영향을 구명코자 수행하였던 바 다음과 같은 결과를 얻었다. 1. 책상조직 및 발달은 적심시기에 따라 발뢰기>개화시>개화만기> 만기 순으로 적심정도에 따라서는 치엽 4매> 치엽 2매> 화뢰 적심 순으로 발달되었다. 2. A급작황에서는 개화만기 B급작황에서는 개화시 치엽 2매를 적심할 때 끽미에 관련있는 전당/니코틴의 비는 9.0, 9.7로 가강 양호하였으며, 방향성 물질인 석유에텐추출물을 9.9%, 8.4%로 가장 높게 나타났다. 3. 품질에 크게 영향하는 요인은 생태조직과 건조엽중 내용성분으로 생태조직의 구성형질들이 품질에 직접 영향하는 효과를 보면 책상조직 43.2%, 해면조직 26.5%, 조직비 17.7%, 엽후 6.7%, 세포간극율 3.1 %, 엽형지수 2.8% 순이며, 내용성분 형질은 니코틴 40.6%, 전당/니코틴 35.7%, 전당 10.0%, 전질소/니코틴 7.0% 전질소 4.6%, 석유 에텔추출물 2.1% 순으로 품질에 영향을 미쳤다. 4. 양질엽 생산을 위해서는 수량이 10a당 250∼280kg 생산되는 A급작황에서는 개화만기에 치엽 2매 적심을, 200kg 내외 생산되는 B급작황에서는 개화시 치엽 2매를 붙여 적심하는 것이 가장 바람직 할 것으로 생각된다.

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Bacillus firmus NA-1 균주와 Bacillus subtilis G7-D 균주를 이용한 발효비지의 기능성 (Functional Properties of Soybean Curd Residue Fermented by Bacillus sp.)

  • 오수명;김찬식;이삼빈
    • 한국식품영양과학회지
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    • 제35권1호
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    • pp.115-120
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    • 2006
  • 일본 청국장에서 분리된 Bacillus firmus NA-1과 재래청국장에서 분리 한 Bacillus subtilis GT-D를 이용하여 전지활성 생 대두미세분말(MFS)첨가 및 발효시간에 따른 비지 발효물의 혈전용해효소, 가수분해효소, 점질물, 펩타이드 생산 및 풍미개선 효과를 알아보았다. $84\%$의 수분함량을 포함하는 비지에 대두미세분말을 10, 15, $20\%$ 첨가함으로써 78, 74, $70\%$로 수분함량을 감소시킬 수 있으며, 발효시간이 경과할수록 tyrosine함량이 증가하였으며, B. firmus NA-1 균주보다는 B. subtilis GT-D 균주를 사용하는 경우에 높은 값을 보였다. 발효비지의 점조도는 B. firmus NA-1 균주를 이용한 발효물이 높은 값을 보였으며, 두 균주 모두 MFS $20\%$를 첨가한 후 26시간 발효한 발효물에서 2.18, $0.35\;Pa{\cdot}s^n$로 가장 높은 점조도 값을 나타내었다. 혈전용해효소 역시 B. firmus NA-1 균주를 이용한 비지 청국장에서 $10\%$ 이상의 높은 활성을 보였으며, 발효 22시간까지 증가하다가 26시간 부터는 큰 변화가 없거나 감소하는 경향을 보였다. 따라서 $20\%$의 MFS를 첨가한 후 $42^{\circ}C$에서 22시간 동안 발효하는 것이 발효취 생성을 최소화하는 조건이라 사료되었다. 비지청국장의 동결건조는 청국장 냄새 및 수분함량을 $6\%$ 수준으로 줄일 수 있었으며, 혈전용해효소의 활성을 포함하였다. B. firmus NA-1 균주를 이용한 시료에서는 615 unit/g의 가장 높은 protease의 활성을 보였으며, B. subtilis GT-D 균주를 이용한 시료에서는 $1903\;mg\%$의 tyrosine 함량 및 180 unit/g의 a-amylase의 활성을 나타내었다.

The genial tubercle: A prospective novel landmark for the diagnosis of mandibular asymmetry

  • Lee, Seung-Youp;Choi, Dong-Soon;Jang, Insan;Song, Geun-Su;Cha, Bong-Kuen
    • 대한치과교정학회지
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    • 제47권1호
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    • pp.50-58
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    • 2017
  • Introduction: Identifying menton (Me) on posteroanterior cephalograms and three-dimensional (3D) cone-beam computed tomography (CBCT) images is difficult, because the midpoint of the symphyseal area is not identifiable after the mandibular symphysis fuses at an early age. The aim of this study was to evaluate the reliability of the identification of the genial tubercle (GT) in patients with mandibular asymmetry and to compare it with that of the traditional landmark, Me. Methods: The samples comprised 20 CBCT images of adults with mandibular asymmetry. Two examiners performed the identifications and measurements. Me and GT were marked, and the anteroposterior, vertical, and transverse distances to the three reference planes were measured on 3D-reconstructed CBCT images. The intra- and inter-examiner reliability of landmark identification of Me and GT were assessed using the intraclass correlation coefficient (ICC) and Bland-Altman plots. Results: The Me and GT landmarks showed excellent reliability ($ICC{\geq}0.993$) three-dimensionally. In the transverse evaluation, the ICC values of the GT (range, 0.997-0.999) tended to be slightly higher than those of Me (range, 0.993-0.996). In the Bland-Altman plots for the two separate assessments, Me showed a maximum error of 1.76 mm in the transverse direction, whereas the GT showed a maximum error of 0.96 mm in the 95% limit. Conclusions: Our results suggest that both Me and GT are clinically reliable and equally useful landmarks for the evaluation of mandibular asymmetry on CBCT images.

Pilot Scale Assessment of DOC and THMs Removal in Conventional Water Treatment System

  • Lee, Choong-Dae;Lee, Yoon-Jin
    • 한국환경과학회지
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    • 제15권9호
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    • pp.829-834
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    • 2006
  • This research aims to investigate the behavior of organic matter that causes bacterial re-growth and the formation of disinfectant by-products such as THM in water treatment, and to optimize conditions for a more efficient and conventional water facility. THM removed 51 % and 12 % through coagulation/sedimentation and filtration using a selected conventional system. In this experiment, the removal ratio of DOC was highest at 68 % when the Gt value was 42,000 and lowest at 41 % when the Gt value was 30,000. 77-84 % of total DOC was removed during coagulation/sedimentation, and 15-23 % was removed during filtration. When Gt values were between 30,000 and 66,000, over 50 % of high molecular matter above 10 K during coagulation/sedimentation was removed. Turbidity removed 98 % when the G1 value was 66,000. As the Gt value increased, the turbidity removal ratio increased. Turbidity removed over 20 % during the filtration process.

Effect of Glycyrrhizae Radix on the Glucuronidation in Rat Liver

  • Moon, Aree;Lee, Mi-Kyung;Kim, Seung-Hee;Kim, Young-Choong;Lee, Song-Deuk
    • Archives of Pharmacal Research
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    • 제18권5호
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    • pp.320-324
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    • 1995
  • Pretreatment of Glycyrrhizae Radix(GR) to male Sprague-Dawley rats was demonstrated to increase excretion of acetaminophen-glucuronide ocnjugate when bile nad urine were assayed after administration of acetaminophen. In order to study the effect of GR on the glucuronidation in rats, we examined enzymatic activities of hepatic UDP-glucuronosyl-transferases (UDP-GT1 and UDP-GT2) and intracellular concentrations of hepatic UDP-glucuronic acid (UDP-GA), upon the administration of GR (1 g/kg body weight, p.o.) or glycyrrhizin (23 mg/kg body weight, p.o.) a major component of GR, for 6 days. GR and glycyrrhizin caused increases in specific activities of UDP-GT2 111% and 96% respectively. Specific activity of UDP-GT1 was increased 25% by GR treatment whereas it was not significantly increased by glycyrrhizin. Concentrations of UDP-GA were increased 257% by GR and 484% by glycyrrhizin. These data indicate that GR activated glucuronidation and thus suggest the possibility that GR may influence detoxification of xenobiotics in rat liver.

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Multiplex PCR Detection of the GT73, MS8xRF3, and T45 Varieties of GM Canola

  • Kim, Jae-Hwan;Kim, Tae-Woon;Lee, Woo-Young;Park, Sun-Hee;Kim, Hae-Yeong
    • Food Science and Biotechnology
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    • 제16권1호
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    • pp.104-109
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    • 2007
  • A multiplex polymerase chain reaction (PCR) method was developed to simultaneously detect three varieties of genetically modified (GM) canola. The construct-specific primers were used to distinguish the following three varieties of GM canola; GT73, MS8xRF3, and T45, using multiplex PCR. The FatA (fatty acyl-ACP thioesterase) gene was used as an endogenous canola reference gene in the PCR detection. The primer pair Canendo-FIR containing a 105 bp amplicon was used to amplify the FatA gene and no amplified product was observed in any of the 15 different plants used as templates. The GT73-KHUF1/R1 primer recognized the 3'-flanking region of GT73, resulting in an amplicon of 125 bp. The Barstar-F1/MS8xRF3-R primer recognized the junction region of bars tar and the NOS terminator introduced into MS8xRF3, resulting in a 162 bp amplicon, and the T45-F2/R2 primer recognized the junction region of PAT and the 35S terminator introduced into T45, resulting in an amplicon of 186 bp. This multiplex PCR allowed for the detection of construct-specific targets in a genomic DNA mixture of up to 1% GM canola containing GT73, MS8xRF3, and T45.

쌀 Glutelin 유전자군의 구조 및 발현조절 (Sturcture of the Rice Glutelin Multigene Family and Its Expression)

  • 황영수
    • 한국식물학회:학술대회논문집
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    • 한국식물학회 1987년도 식물생명공학 심포지움 논문집 Proceedings of Symposia on Plant Biotechnology
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    • pp.261-282
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    • 1987
  • Plants store a significant amount of their nitrogen, sulfur and carbon reserves as storage proteins in seed tissues. The major proteins present in rice seeds are the glutelins. Glutelins are initially synthesized at 4-6 days postanthesis and deposited into protein bodies via Golgi apparatus. Based on nucleic acid sequences and Southern blot analysis, the three isolated glutelin genomic clones were representative members of three gene subfamilies each containing 5 to 8 copies. A comparison of DNA sequences displayed by relevant regions of these genomic clones showed that two subfamilies, represented by clones, Gt1 and Gt2, were closely, related and probably evolved by more recent gene duplication events. The 5' flanking and coding sequences of Gt1 and Gt2 displayed at least 87% homolgy. In contrast, Gt3 showed little or no homolgy in the 5' flanking sequences upstream of the putative CAAT boxes and exhibited significant divergence in all other portions of the gene. Conserved sequences in the 5' flanking regions of these genes were identified and discussed in light of their potential regulatory role. The derived primary sequences of all three glutelin genomic clones showed significant homology to the legume 11S storage proteins indicating a common gene origin. A comparison of the derived glutelin primary sequences showed that mutations were clustered in three peptide regions. One peptide region corresponded to the highly rautable hypervariable region of legume peptide region of legume 11S storage proteins, a potential target area for protein modification. Expression studies indicated that glutelin mRNA transcripts are differentially accumulated during endosperm development. Promoterss of Gt2 and Gt3 were functional as they direct transient expression of chloramphenicol acetyltransferase in cultured plant cell.

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Quantification of Genetically Modified Canola GT73 Using TaqMan Real-Time PCR

  • Kim, Jae-Hwan;Song, Hee-Sung;Kim, Dong-Hern;Kim, Hae-Yeong
    • Journal of Microbiology and Biotechnology
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    • 제16권11호
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    • pp.1778-1783
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    • 2006
  • Event-specific PCR detection methods are the primary trend in genetically modified (GM) plant detection owing to their high specificity based on the flanking sequence of the exogenous integrant. Therefore, this study describes a real-time PCR system for event-specific GM canola GT73, consisting of a set of primers, TaqMan probe, and single target standard plasmid. For the specific detection of GT73 canola, the 3'-integration junction sequence between the host plant DNA and the integrated specific border was targeted. To validate the proposed method, test samples of 0, 1, 3, 5, and 10% GT73 canola were quantified. The method was also assayed with 15 different plants, and no amplification signal was observed in a real-time PCR assay with any of the species tested, other than GT73 canola.

현지초(Geranium thunbergii) 추출물의 생리활성 및 Raw 264.7 cells에서의 항염활성 검증 (Verification of the Physiological Activity of Geranium thunbergii Extract and Anti-inflammatory Activity in Raw 264.7 Cells)

  • 박승미;오민정;이진영
    • 생명과학회지
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    • 제34권1호
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    • pp.28-36
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    • 2024
  • 본 연구에서는 현재까지 화장품 소재로써 다양한 연구가 진행되지 않은 현지초 추출물의 효능평가 및 항염 관련 활성 연구를 진행하였다. 현지초 추출물의 항산화능을 확인하기 위해 전자공여능 및 ABTS+ 라디칼 소거능을 측정한 결과, 각각 50 ㎍/ml의 농도에서 91%, 94%를 나타내어 항산화능이 우수함을 확인할 수 있었다. 미백활성 측정을 위해 tyrosinase 저해활성 측정을 실시하였으며 최고 농도인 1,000 ㎍/ml에서 24.8%의 저해능이 나타났다. 현지초 추출물의 주름개선 활성을 알아보기 위해 elastase 및 collagenase 저해활성 측정을 실시하였으며 그 결과, 각각 최고 농도인 1,000 ㎍/ml에서 30.6%, 90%의 저해능이 나타났고 collagenase 저해활성에서 우수한 저해능을 확인할 수 있었다. 세포 실험 진행을 위해 현지초 추출물 처리에 따른 대식세포 Raw 264.7의 생존율을 MTT assay에 의거하여 진행하였으며 100 ㎍/ml의 농도에서 83.6% 이상의 세포 생존율을 나타내어 이하의 세포 관련 실험 진행은 100 ㎍/ml 이하의 농도의 현지초 추출물을 가하여 실험을 실시하였다. NO assay에 의하여 현지초 추출물 처리에 따른 NO 생성 저해 활성을 측정한 결과, 100 ㎍/ml의 농도에서 74.9%의 저해율을 확인하였다. 단백질 발현 억제능을 알아보기 위해 western blot을 진행하였으며 현지초 추출물은 COX-2 및 iNOS 두 인자 모두 농도의존적으로 단백질 발현량이 저해됨을 확인할 수 있었다. 이러한 결과들에 의해 현지초 추출물은 항염 관련 기능성 화장품 소재로써 활용 가능성이 있다고 사료된다.

태양광 모듈의 투과특성과 효율과의 연관성에 대한 연구 (Study on relation of transmittance characteristics and efficiency for Photovoltaic Module)

  • 정인성;정은석;김정근;이범수;김종일;김철주
    • 한국전기전자재료학회:학술대회논문집
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    • 한국전기전자재료학회 2009년도 하계학술대회 논문집
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    • pp.453-453
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    • 2009
  • Wafer 태양전지와 Back sheet 및 기타 소재를 사용하는 기존의 Photovoltaic Module은 투과성이 존재하지 않으므로 본 논문에서는 태양전지 모듈의 투과특성을 발휘할 수 있는 Glass to Glass (GtG) Type의 Photovoltaic module에 대해 그 투과 특성 및 효율과의 관계를 분석하였다. 먼저 Module용 소재 중 Poly vinyl butyral (PVB) 및 Ethylene vinyl acetate(EVA) sheet의 Transmittance와 Haze 특성을 분석하였다. GtG 타입의 Photovoltaic Module은 약 90%정도의 투과율을 갖는 강화유리 및 Haze가 없는 PVB sheet를 사용하여 1m $\times$ 1m 크기로 제작하였다. GtG 타입으로 제조한 모둘 중 Cell 16EA를 사용한 모듈은 Cell 25EA를 사용한 모듈에 비해서 36% 투과율이 증가하였으나 효율 면에서 38%감소하였다. 최종적으로 GtG 타입 Module의 효율과 투과율에 관련된 식을 각각 정립하였다.

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