• 제목/요약/키워드: pl gene

검색결과 75건 처리시간 0.026초

알칼리 내성 Bacillus sp. YA-14 유래의 중복 Promotor를 이용한 재조합 Plasmid로부터의 Pectate Iyase의 발현

  • 박희경;함병권;유주현;배동훈
    • 한국미생물·생명공학회지
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    • 제25권6호
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    • pp.571-579
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    • 1997
  • For the overproduction of pectate lyase (PL), the recombinant plasmid pl2BS fl which has strong promoter from alkali-tolerent Bacillus sp. YA-14 was used. In order to overexpress the pectate lyase by the action of overlapping strong promoter in pl2BS$\Delta$fl, 1.6 kb of PL gene was inserted into pl2BS$\Delta$fl to form pl2BS$\delta$f1-PL and the enzyme was expressed. But decreased expression efficiency of the PL gene was observed and it was due to the presence of the transcription terminator region on the upstream of the PL gene. The transcription terminator of the PL gene in pl2BS$\delta$f1-PL was removed and the resulting plasmid p12BS$\Delta$fl$\Delta$PL was formed. Bacillus subtilis 207-25 harboring the recombinant plasmid, p12BS$\Delta$fl$\Delta$PL, revealed increased expression efficiency with chloramphenicol induction when cat-86 was used as a reporter gene.

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흰쥐 태반에서 Placental Lactogen I과 II 그리고 Pit-1의 유전자 발현에 미치는 에스트로겐의 영향 (Effect of Estrogen on the Gestational Profiles in Gene Expression of Placental Lactogen I, II and Pit-i in the Rat Placenta)

  • 정진권;강성구;강해묵;이병주
    • 한국동물학회지
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    • 제39권1호
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    • pp.115-121
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    • 1996
  • 임신중기에서 발기에 이르는 흰쥐의 태반에서 Placental Lactogen I (PL-I), II 그리고 Pit-1 의 유전자 발현 변화를 Northern blot hybridization으로 조사하였다. 그 결과, 임신시기에 따라 PL-I과 PL-II의 mRNA 양과 크기에 변화가 나타났다. 이들 유전자 발현에 미치는 에스트로겐의 영향을 조사하기 위하여, 임신 14일째 쥐의 난소를 제거하고(OVX), 이후 매일 에스트로겐을 투여한 후 (OVX+E), 임신 18일째 태반을 회수하여 PL-I, II 그리고 Pit-1의 유전자 발현을 Northern blot hybridization으로 조사하였다. OVX 군의 경우, PL-I의 mRNA 크기는 1 kb에서 1.3 kb로 PL-II의 mRNA는 0.6kb에서 1 kb로 변화하였다. OVX+E 군에서는 PL-I과 PL-II의 mRNA가 정상대조군과 같은 상태로 환원하였다. 정상대조군에 비하여 OVX와 OVX+E 군에서 PL-I과 PL-II의 mRNA 크기에는 영향을 미치지 못한 반면, mRNA 양은 난소제거시 감소하였다가, 에스트로겐을 투여하면, 부분적으로 회복되는 경향을 보였다. 이러한 본 실험의결과는 에스트로겐이 PL-I과 PL-II의 RNA splicing이나 polyadenylation 등을 포함한 유전자 발현에 영향을 미치며, Pit-1이 이 과정에 개입하는 것을 시사하는 것이다.

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옥수수 종피의 안토시아닌 합성을 조절하는 R 유전자 구성요소의 구명 (Identification of the Maize R Gene Component Responsible for the Anthocyanin Biosynthesis of Kernel Pericarp)

  • 김화영
    • 한국육종학회지
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    • 제42권1호
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    • pp.50-55
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    • 2010
  • 옥수수 R 유전자의 대립인자 중 하나인 R-r:standard (R-r:std)는 종자 호분층의 안토시아닌 합성을 조절하는 S subcomplex와 종자 이외 식물체부위의 안토시아닌 합성을 조절하는 P component로 구성되어 있으며, S subcomplex는 S1 및 S2 component로 구성되어 있다. R 유전자의 대립인자 중 일부는 Pl 유전자가 존재할 경우 종피의 안토시아닌 합성을 유도한다. 따라서 Pl 유전자가 존재할 경우 옥수수 종피의 안토시아닌 합성을 유도하는 R 유전자의 구성요소를 구명하고자 종피의 안토시아닌 합성에 미치는 서로 다른 R 인자들의 효과를 분석하였다. R-ch와 r-ch 인자는 유사한 정도의 착색 효과를 보였으며, R-r:Ecuador (R-r:Ec)는 이들보다 짙은 착색효과를 나타내었다. S subcomplex의 기능은 상실하였으나 정상적인 P component를 보유하고 있는 것으로 추정되는 r-ch는 Pl 유전자가 존재할 경우 종피의 색소합성 기능을 유지하고 있으나, S subcomplex의 기능은 정상이나 P component의 기능은 잃어버린 것으로 추정되는 R-r:Ec 유래 인자 R-g:g1111는 Pl 유전자가 존재할 경우에도 종피가 착색되지 않았다. 더욱이 R-ch와 r-ch 인자의 PCR 분석 결과, R-ch는 P와 S1 component를 보유하고 있으나, r-ch는 S1을 보유하고 있지 않는 것으로 나타났다. 따라서 R 유전자의 구성요소 중 P component가 종피의 안토시아닌 합성에 관여하는 구성요소로 추정되었다.

Construction of a Genetic System for Streptomyces albulus PD-1 and Improving Poly(ε-ʟ-lysine) Production Through Expression of Vitreoscilla Hemoglobin

  • Xu, Zhaoxian;Cao, Changhong;Sun, Zhuzhen;Li, Sha;Xu, Zheng;Feng, Xiaohai;Xu, Hong
    • Journal of Microbiology and Biotechnology
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    • 제25권11호
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    • pp.1819-1826
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    • 2015
  • Poly(ε-ʟ-lysine) (ε-PL) is a novel bioactive polymer secreted by filamentous bacteria. Owing to lack of a genetic system for most ε-PL-producing strains, very little research on enhancing ε-PL biosynthesis by genetic manipulation has been reported. In this study, an effective genetic system was established via intergeneric conjugal transfer for Streptomyces albulus PD-1, a famous ε-PL-producing strain. Using the established genetic system, the Vitreoscilla hemoglobin (VHb) gene was integrated into the chromosome of S. albulus PD-1 to alleviate oxygen limitation and to enhance the biosynthesis of ε-PL in submerged fermentation. Ultimately, the production of ε-PL increased from 22.7 g/l to 34.2 g/l after fed-batch culture in a 5 L bioreactor. Determination of the oxygen uptake rate, transcriptional level of ε-PL synthetase gene, and ATP level unveiled that the expression of VHb in S. albulus PD-1 enhanced ε-PL biosynthesis by improving respiration and ATP supply. To the best of our knowledge, this is the first report on enhancing ε-PL production by chromosomal integration of the VHb gene in an ε-PL-producing strain, and it will open a new avenue for ε-PL production.

구강 편평세포암종에서 태반성장인자의 발현 (EXPRESSION OF PLACENTA GROWTH FACTOR IN THE ORAL SQUAMOUS CELL CARCINOMA)

  • 이상구;김철환
    • Maxillofacial Plastic and Reconstructive Surgery
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    • 제31권1호
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    • pp.27-34
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    • 2009
  • Angiogenesis is essential for solid tumor growth and progression. Among the pro-angiogenetic factors, vascular endothelial growth factor(VEGF), also known as vascular permeability factor, is the most important as a mitogen for vascular endothelium. The VEGF family of molecules currently consists of six growth factors, VEGF-A, VEGF-B, VEGF-C, VEGF-D, VEGF-E, and placenta growth factor(PlGF). Over-expression of PlGF is associated with angiogenesis under pathological conditions such as ischemia, inflammation, and cancer. Hence, the goal of this study is to identify the correlation of clinicopathlogical factors and the up-regulation of PlGF expression in oral squamous cell carcinoma. We studied the immunohistochemical staining of PlGF, PlGF gene expression and a real time quantitative RT-PCR in 20 specimens of 20 patients with oral squamous cell carcinoma. The results were as follows. 1. In the immunohistochemical study of poorly differentiated and invasive oral squamous cell carcinoma, the high level staining of PlGF was observed. And the correlation between immunohistopathological PlGF expression and histological differentiation of specimens was significant (Pearson correlation analysis, significance [r] >0.6, P < .05). 2. In the PlGF gene RT-PCR analysis, PlGF expression was more in tumor tissue than in adjacent normal tissue. Paired-samples analysis determined the difference of PlGF mRNA expression level between the cancer tissue and the normal tissue (Student's t - test, P < .05) These findings suggest that up-regulation of the PlGF gene may play a role in progression and local metastasis in invasive oral squamous cell carcinoma.

알카리 내성 Bacillus sp. YA-14의 Pectate Lyase 유전자의 클로닝과 발현 (Cloning of Pectate Lyase Gene of Alkali-tolerant Bacillus sp. YA-14 and Its Expression in Escherichia coli)

  • Yu, Ju-Hyun;Park, Yoon-Suk;Kim, Jin-Man;Kong, In-Soo;Chung, Yong-Joon
    • 한국미생물·생명공학회지
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    • 제16권4호
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    • pp.316-319
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    • 1988
  • 토양으로부터 분리한 알카리내성 Bacillus sp. YA-14의 Pectate lyase(PL) 유전자를 E. coli에 cloning하여 제조한 재조합 plasmid pYPC29는 삽입 된 1.6kb 단편내에 PL 유전자를 함유하고 있었으며, 이 외래 DNA가 Bacillus sp. YA-14의 chromosomal DNA에서 유래된 것임을 Southern hybridization을 통하여 확인하였다. 재조합 plasmid pYPC29는 E. coli내에서 안정하게 존재하였으며 이를 함유한 재조합체의 전체 PL 활성 중 약 70%가 periplasmic space에 존재하였다.

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Bacillus subtilis DT134의 카드뮴 저항성 (Characteristics of Cadmium-Resistant Bacillus subtilis DT134)

  • 윤경표
    • KSBB Journal
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    • 제13권4호
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    • pp.383-390
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    • 1998
  • Bacillus subtilis DT134 was resistant to 50-fold higher concentration of cadmium ions (Cd2+) than cadmium-sensitive B. subtilis BD224 in Luria Broth (LB) medium. Minimal inhibition concentration test in LB agar plates also showed similar results. The elevated cadmium resistance of B. subtilis DT134 strongly suggested a possible existence of cadmium resistance gene in it. Southern blot with Staphylococcus aureus cadA gene fragment (757 bp NlaIV-XmnI cadA DNA fragment) as probe was carried out to test the existence and similarity of the gene. In high stringency condition, there was no detectable signal, but in low stringency, a strong signal specific to the cadA probe could be detected. These results strongly suggested that there was some similarity between total DNA of B. subtilis DT134 and S. aureus pl258 in terms of cadmium resistance gene and the resistance mechanism might be an efflux mechanism. The subsequent efflux experiment showed that the cadmium resistance mechanism of B. subtilis DT134 was also due to the efflux of cadmium.

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역전사효소(逆轉寫酵素) 유전자(遺傳子)의 cloning 에 관(關)한 연구(硏究) (Cloning of Reverse Transcriptase Gene of Avian Sarcoma Virus)

  • 김용웅;김광식;서용택
    • Applied Biological Chemistry
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    • 제31권3호
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    • pp.219-225
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    • 1988
  • Avian Sarcoma Virus의 plasmid DNA중(中)의 역 이사효소의 유전자(遺傳子)를 온도의존성(溫度依存性) 발현(發現) vector인 pPL-lambda에 cloning하여 온도(溫度)에 민감한 phage ${\lambda}$의 repressor인 cI857 gene을 갖고 있는 bacteriophage lysogen인 N4830에 transformation시켰다. transformant를 pL promoter의 발현(發現)을 억제(抑制)하는 저온(低溫)$(28^{\circ}C)$에서 배양(培養)시킨 뒤, 이 repressor를 억제(抑制)하여 transcription을 촉진(促進)하게 하는 고온(高溫)$(42^{\circ}C)$에서 배양(培養)시킨 다음 균체(菌體)를 회수(回收)하여 RNA를 추출(抽出)하고 분석(分析)을 한 결과(結果) 도입(導入)된 역전사 효소 유전자(遺傳子)의 전사(轉寫)가 고온(高溫)에서 증대(增大)되었다.

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시엽(枾葉)의 멜라닌 생성 억제와 작용기전에 관한 연구 (Inhibitory Effect of Persimmon Leaves on Melanin Synthesis and its Action Mechanism in B16F10 cells)

  • 장두현;유동열
    • 대한한방부인과학회지
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    • 제22권2호
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    • pp.43-59
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    • 2009
  • Purpose: This study was performed to determine the inhibitory effect of Persimmon Leaves extract (PL) on melanin synthesis in B16F10 melanoma cells B16F10. Methods: The inhibitory effects of PL on melanin synthesis were determined by in vitro assay. To elucidate inhibitory effects of PL on melanin synthesis, we determined the melanin release and melanin production in B16F10. And to investigate the action mechanism, we assessed the gene expression of tyrosinase, TRP-1, TRP-2, PKA, PKC${\beta}$, ERK-1, ERK-2, AKT-1, MITF in B16F10. Results: 1. PL inhibited melanin release, melanin production in B16F10. 2. PL inhibited tyrosinase activity in vitro and in B16F10. 3. PL suppressed the expression of tyrosinase, TRP-1, TRP-2 in B16F10. 4. PL suppressed the expression of PKA, PKC${\beta}$ in B16F10. 5. PL increased the expression of ERK-1, ERK-2, AKT-1 in B16F10. 6. PL suppressed the expression of MITF in B16F10. Conclusion: From these results, it may be concluded that PL is possesed of the antimelanogenetic effects.

Histone deacetylation effects of the CYP1A1 promoter activity, proliferation and apoptosis of cells in hepatic, prostate and breast cancer cells

  • K.N. Min;K.E. Joung;M.J. Cho;J.Y. An;Kim, D.K.;Y.Y. Sheen
    • 한국응용약물학회:학술대회논문집
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    • 한국응용약물학회 2003년도 Annual Meeting of KSAP : International Symposium on Pharmaceutical and Biomedical Sciences on Obesity
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    • pp.91-91
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    • 2003
  • We have studied the mechanism of action of TCDD on CYP1A1 promoter activity in both Hepa I and MCF-7 cells using transient transfection system with plAl-Luc reporter gene. When HDAC inhibitors, such as trichostatin A, HC toxin and a novel HDAC inhibitor, IN2001 were cotreated with TCDD to the cells transfected with plAl-Luc reporter gene, the basal promoter activity of CYP1A1 was increased by HDAC inhibitors. Also, in MCF-7 human breast cancer cells, HDAC inhibitors, such as IN2001 and trichostatin A increased the basal activity of CYP1A1 promoter but TCDD stimulated CYP1A1 promoter activity was not changed by HDAC inhibitors. And, in stably-transfected Hepa I cells with plAl-Luc, HDAC inhibitors increased the basal promoter activity only.

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