• Title/Summary/Keyword: Yeast Cell

검색결과 1,302건 처리시간 0.037초

효모의 세포벽에 대한 $Glucanex^{(R)}$ 200G의 영향 (Effect of $Glucanex^{(R)}$ 200G on Yeast Cell Wall)

  • 김광석;장정은;윤현식
    • KSBB Journal
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    • 제19권4호
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    • pp.288-290
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    • 2004
  • 효모의 종류에 따라 세포벽의 composition이 다른 것으로 알려져 있으나 이에 대한 체계적인 연구는 아직 이루어지지 않고 있다. 본 연구에서는 한국 유전자은행 (KCTC)과 한국미생물 보존센터 (KCCM)에서 구입한 15종류의 효모를 $Glucanex^{(R)}$ 200G로 처리한 후 생균수를 측정하여 상대적인 저항성을 비교하였다. 그 결과 Trigonopsis variabilis나 Sporidiobolus pararoseus는 $\beta$-glucanase에 대한 저항성이 높았으며 Pichia stiptis나 Filibasidium cpasuligenum은 $\beta$-glucanase에 대한 저항성이 낮았다. $\beta$-glucan의 함량이 높은 세포는 높은 농도의 $\beta$-glucanase 농도에서도 저항성을 가지므로 이를 바탕으로 여러 효모의 세포벽의 상대적인 $\beta$-glucan 함량을 추정할 수 있다.

Genetic Screening for Plant Cell Death Suppressors and Their Functional Analysis in Plants

  • Yun, Dae-Jin
    • 한국생명과학회:학술대회논문집
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    • 한국생명과학회 2005년도 국제학술심포지움 The 44th Annual Meeting of Korean Society for Life Science
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    • pp.23-36
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    • 2005
  • Bax, a mammalian pro-apoptotic member of the Bcl-2 family, induces cell death when expressed In yeast. To investigate whether .Bax expression can induce cell death in plant, we produced transgenic Arabidopsis plants that contained murine Bax cDNA under control of a glucocorticoid-inducible promoter. Transgenic plants treated with dexamethasone, a strong synthetic glucocorticoid, induced Bax accumulation and cell death, suggesting that some elements of cell death mechanism by Bax may be conserved among various orgarusms. Therefore, we developed novel yeast genetic system, and cloned several Plant Bax Inhibitors (PBIs). Here, we report the function of two PBIs In detail. PBIl is ascorbate peroxidase (sAPX). Fluorescence method of dihydrorhodamine123 oxidation revealed that expression of Bax in yeast cells generated reactive oxygen species (ROS), and which was greatly reduced by co-expression with sAPX. These results suggest that sAPX inhibits the generation of ROS by Bax, which in turn suppresses Bax-induced cell death in yeast. PBI2 encodes nucleoside diphosphate kinase (NDPK). ROS stress strongly induces the expression of the NDPK2 gene in Arabidopsis thaliana (AtNDPK2). Transgenic plants overexpressing AtNDPK2 have lower lovels of ROS than wildtype plants. Mutants lacking AtNDPK2 had higher levels of ROS than wildtype. H$_{2O2}$ treatment induced the phosphorylation of two endogenous proteins whose molecular weights suggested they are AtMPK3 and AtMPK6. In the absence of H2O2 treatment, phosphorylation of these proteins was slightly elevated in plants overexpressing AtNDPK2 but markedly decreased In the AtNDPK2 deletion mutant. Yeast two-hybrid and in vitro protein pull-down assays revealed that AtNDPK2 specifically interacts with AtMPK3 and AtMPK6. Furthermore, AtNDPK2 also enhances the MBP phosphorylation activity of AtMPK3 i'n vitro. Finally, constitutive overexpression of AtNDPK2 in Arabidopsis plants conferred an enhanced tolerance to multiple environmental stresses that elicit ROS accumulation In situ. Thus, AtNDPK2 appears to play a novel regulatory role in H2O2-mediated MAPK signaling in plants.

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초소형 평면 전극 구조에서 세포에 작용하는 DIELECTROPHORETIC FORCE의 해석 및 실험 (ANALYSIS AND EXPERIMENT OF DIELECTROPHORETIC FORCE ON A CELL IN A PLANAR ELECTRODE STRUCTURE)

  • 최정훈;이상욱;김용권
    • 대한전기학회:학술대회논문집
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    • 대한전기학회 1995년도 추계학술대회 논문집 학회본부
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    • pp.597-599
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    • 1995
  • We have analyzed the dielectrophoretic(DEP) force on a cell in a micro planar electrode structure. We fabricate a micro planar electrode structure using micro machining technology and measure the motion of a cell that is accelerated by DEP force. DEP force on a cell is calculated by curve fitting the motion of a cell. Radish and yeast are used for the experiment. In case of radish, DEP force is increased as the voltage and the frequency is increased, and in case of yeast, DEP force is increased only as the voltage is increased DEP force on a yeast does not vary when the frequency varies from 1 MHz to 3 MHz. The result will be helpful to the manipulation of cells using DEP force.

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석유탄화수소를 이용한 단세포단백질의 생산에 관한 연구 3 (Production of Single-Cell Protein on Petroleum Hydrocarbon)

  • 변유량;권태완
    • 미생물학회지
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    • 제9권3호
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    • pp.95-102
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    • 1971
  • The growth characteristics of Candida tropicalis KIST 351 on gas oil substrate under different culture conditions were investigated and the preliminary animal feeding experiments using this yeast as a partial substitute of fish meal was also conducted. The yeast assimilates effectively n-paraffins in gas oil ranging from $C_{16}$ to $C_{16}$ with its maximum cell growth at $33^{\circ}C$ and pH 5.5 with aeration of 3 vvn and agitation of 900 rpm. The optimal concentrations of nitrogen sources, $HK_2PO_4$ and $Na_2HPO$ were 4, 2 and 0.5g/1, respectively. Ferrous sulfate, manganese sulfate and zinc sulfate showed positive effect to cell growth with the optimal range of 5-10 ppm. In the feeding experiment with 3 and 5% incorporation of the gas oil grown yeast, neither adverse effects on growth of chicks nor toxic effect were observed. Protein content of the dried cell was 58.8% and its amino acid composition compared well with other single-cell protein products and FAO reference protein.

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Chemical composition and standardized ileal digestibility of crude protein and amino acid in whole yeast and autolyzed yeast derived from sugarcane ethanol production fed to growing pigs

  • Kaewtapee, Chanwit;Jantra, Nontawut;Petchpoung, Krittaya;Rakangthong, Choawit;Bunchasak, Chaiyapoom
    • Animal Bioscience
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    • 제35권9호
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    • pp.1400-1407
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    • 2022
  • Objective: This research determined the chemical composition and the apparent and standardized ileal digestibility (AID and SID) of crude protein (CP) and amino acids (AA) in whole yeast and autolyzed yeast derived from sugarcane ethanol production fed to growing pigs. Methods: Six growing pigs were randomly allocated in a replicated 3×3 Latin square design with 3 diets and 3 periods of 7 days each, resulting in a total of 6 experimental replications. Three assay diets were formulated using whole yeast, autolyzed yeast, or soybean meal as the sole sources of dietary CP and AA. Pigs were allowed to adapt to the assay diets for 5 days. Thereafter, ileal digesta samples were collected continuously for 8 hours on days 6 and 7. Results: There was no difference in the chemical composition between whole yeast and autolyzed yeast, but whole yeast had low digestibility of CP and AA due to the presence of a rigid cell wall. As conducting autolysis can induce cell wall damage, the AID and SID of CP and AA were greater in autolyzed yeast than in whole yeast. Conclusion: The information obtained on the SID of CP and AA in both yeast products can be used for the accurate estimation of the bioavailability of CP and AA in feed formulations. The yeast products derived from sugarcane ethanol production are an alternative protein source in pig diets.

Salmonella sp. 의 신속한 동정을 위한 증진배양의 개선에 관한 연구

  • 김기태;김태우;육순학;이영호;백운화
    • 한국미생물·생명공학회지
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    • 제24권6호
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    • pp.647-651
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    • 1996
  • The development of an enrichment method for the rapid and effective identification of Salmonella spp. in sewage or food was studied. As a growth factor for Salmonella, 10 mM cyclic adenosine monophosphate (cAMP) in trypticase soy broth with 0.6% yeast extract (TSBYE) increased cell number five-folds and 0.6% yeast extract in selenite broth increased cell number ten-folds of control. Bile salts in selenite broth was tested for the selection of S. enteritidis in a mixture with Staphylococcus aureus, Pseudomonas aeruginosa, Lactobacillus plantarum and Escherichia coli. The latter four strains were effectively inhibited at 0.1% bile salt. A two-step culture method was used to enrich Salmonella spp.; a primary-enrichment and secondary- enrichment culture. At a primary-enrichment step, selenite broth with 0.6% yeast extract and 10 mM cAMP was used, and at a secondary-enrichment step, 0.1% bile salt was additionally used. Culture times of a primary- enrichment and a secondary-enrichment step were 8 hr and 6 hr, respectively. In this procedure, cell number increased from 10$^{0.3}$ to 10$^{8.5}$ with inhibition of other strains within 14 hr. In the case of an initial cell concentrarion as low as 10$^{-2}$ cfu/ml, a cell number increased to 10$^{7}$ cfu/ml by using a 10 hr primary-enrichment and 6 hr secondary-enrichment procedure.

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Genetic Relationship between the SPT3 Gene and RAS/cAMP Pathway in Yeast Cell Cycle Control (Genetic relationship between the SPT3 gene and ARS/cAMP pathway in yeast cell cycle control)

  • Shin, Deug-Yong;Yun, Jean-Ho
    • Journal of Microbiology
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    • 제34권2호
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    • pp.158-165
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    • 1996
  • The signal transduction pathways through the RAS gene product and adenyl cyclease play a critical role in regulation of the cell cycle in yeast, Saccharomyces cerevisiae. We examined the genetic relationship between the spt3 gene and ras/cAMP pathway. A mutation in the SPT3 gene suppressed cell cycle arrest at the G1 phase caused by either an inactivation of the RAS or CYR1 gene which encodes a yeast homologue of human ras proto-oncogene or adenyl cyclase, respectively. The phenotypes such as sporulation and heat shock resistancy, that resulted from a partial inactivation of the RAS or CYR1 genes, were also suppressed by the spt3 mutation. Expression of the SSA1 gene encoding one of th heat shock proteins (Hsp70) can be induced by heat shock or nitrogen starvation. Expression of this gene is derepressed in cry1-2 and spt3 mutants. The bcy 1 mutation repressed by the bcy1 mutation, but not in spt3 mutants. These results suggest that the SPT gene is involved in expression of genes that are affected by the RAS/cAMP pathway.

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Comparative analysis of yeast cell viability at exponential and stationary growth phases

  • An, Yejin;Jo, Nayoon;Kim, Hyeji;Nam, Dahye;Son, Woorim;Park, Jinkyu
    • 분석과학
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    • 제35권4호
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    • pp.181-188
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    • 2022
  • This paper describes a comparative analysis of yeast cell viability at exponential and stationary growth phases using multiple conventional techniques and statistical tools. Overall, cellular responses to various viability assays were asynchronous. Results of optical density measurement and direct cell counting were asynchronous both at exponential and stationary phases. Proliferative capacity measurement using SP-SDS indicated that cells at the end of the stationary phase were proliferative as much as exponentially growing cells. Metabolic activity assays using two different dyes concluded that the inside of cells at stationary phase is slightly less reducing compared to that of exponentially growing cells, implying that the metabolic activity imperceptibly declined as cells were aged. These results will be helpful to understand the details of yeast cell viability at exponential and stationary growth phases.

음향방사력을 이용한 효모세포의 크기별 분리 (Size-based Separation of Yeast Cell by Surface Acoustic Wave-induced Acoustic Radiation Force)

  • 라이한 하디 줄리오;무함마드 소반 칸;무스타크 알리;굴람 데스트기르;박진수
    • 한국가시화정보학회지
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    • 제21권3호
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    • pp.93-100
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    • 2023
  • The yeast Saccharomyces cerevisiae (S. cerevisiae) is considered an ideal eukaryotic model and has long been recognized for its pivotal role in numerous industrial production processes. Depending on the cell cycle phases, microenvironment, and species, S. cerevisiae varies in shape and has different sizes of each shape such as singlets, doublets, and clusters. Obtaining high-purity populations of uniformly shaped S. cerevisiae cells is crucial in fundamental biological research and industrial operations. In this study, we propose an acoustofluidic method for separating S. cerevisiae cells based on their size using surface acoustic wave (SAW)-induced acoustic radiation force (ARF). The SAW-induced ARF increased with cell diameter, which enabled a successful size-based separation of S. cerevisiae cells using an acoustofluidics device. We anticipate that the proposed acoustofluidics approach for yeast cell separation will provide new opportunities in industrial applications.

DHA 생산을 위한 Crypthecodinium cohnii의 성장조건 최적화에 관한 연구

  • 김호정;이재영;권태순;양지원
    • 한국생물공학회:학술대회논문집
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    • 한국생물공학회 2001년도 추계학술발표대회
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    • pp.853-854
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    • 2001
  • The purpose of the present study is to find the optimal growth condition of Crypthecodinium cohnii. Using a design of experiments, it was found that the yeast extract was the most significant factor for cell growth. The effect of glucose was less than that of yeast extract and the effect of NaCl was negligible. The highest cell density, 1O.96g/L was obtained at the concentration of yeast extract 7.5g/L.

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