• 호남수학학술지
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• 제27권2호
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• pp.301-315
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• 2005

Let $\{A_u,\;u=0,\;1,\;2,\;{\cdots}\}$ be a sequence of coefficient matrices such that ${\sum}_{u=0}^{\infty}{\parallel}A_u{\parallel}<{\infty}$ and ${\sum}_{u=0}^{\infty}\;A_u{\neq}O_{m{\times}m}$, where for any $m{\times}m(m{\geq}1)$, matrix $A=(a_{ij})$, ${\parallel}A{\parallel}={\sum}_{i=1}^m{\sum}_{j=1}^m{\mid}a_{ij}{\mid}$ and $O_{m{\times}m}$ denotes the $m{\times}m$ zero matrix. In this paper, a functional central limit theorem is derived for a stationary m-dimensional linear process ${\mathbb{X}}_t$ of the form ${\mathbb{X}_t}={\sum}_{u=0}^{\infty}A_u{\mathbb{Z}_{t-u}}$, where $\{\mathbb{Z}_t,\;t=0,\;{\pm}1,\;{\pm}2,\;{\cdots}\}$ is a stationary sequence of linearly positive quadrant dependent m-dimensional random vectors with $E({\mathbb{Z}_t})={{\mathbb{O}}$ and $E{\parallel}{\mathbb{Z}_t}{\parallel}^2<{\infty}$.

• 대한수학회논문집
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• 제21권1호
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• pp.37-43
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• 2006

We prove that $M_1\longrightarrow^f\;M_2$ is an injective representation of a quiver $Q={\bullet}{\rightarrow}{\bullet}$ if and only if $M_1\;and\;M_2$ are injective left R-modules, $M_1\longrightarrow^f\;M_2$ is isomorphic to a direct sum of representation of the types $E_l{\rightarrow}0$ and $M_1\longrightarrow^{id}\;M_2$ where $E_l\;and\;E_2$ are injective left R-modules. Then, we generalize the result so that a representation$M_1\longrightarrow^{f_1}\;M_2\; \longrightarrow^{f_2}\;\cdots\;\longrightarrow^{f_{n-1}}\;M_n$ of a quiver $Q={\bullet}{\rightarrow}{\bullet}{\rightarrow}{\cdots}{\rightarrow}{\bullet}$ is an injective representation if and only if each $M_i$ is an injective left R-module and the representation is a direct sum of injective representations.

• Journal of Applied Biological Chemistry
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• 제42권1호
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• pp.12-18
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• 1999

Sucrose synthase (EC 2.4.1.13) has been purified from the plant cytosolic fraction of chickpea (Cicer arietinum L. cv. Amethyst) nodules. The native enzyme had a molecular mass of $356{\pm}15kD$. The subunit molecular mass was $87{\pm}2kD$, and a tetrameric structure is proposed for sucrose synthase of chickpea nodule. Optimum activities in the sucrose cleavage and synthesis directions were at pH 6.5 and 9.0, respectively. The purified enzyme displayed typical hyperbolic kinetics with substrates in cleavage and synthesis reactions. Chickpea nodules sucrose synthase had a high affinity for UDP ($K_m$, $8.0{\mu}M$) and relatively low affinities for ADP ($K_m$, 0.23 mM), CDP ($K_m$, 0.87 mM), and GDP ($K_m$, 1.51 mM). The $K_m$ for sucrose was 29.4 mM. In the synthesis reaction, UDP-glucose ($K_m$, $24.1{\mu}M$) was a more effective glucosyl donor than ADP-glucose ($K_m$, 2.7 mM), and the $K_m$ for fructose was 5.4 mM. Divalent cations, such as $Ca^{2+}$, $Mg^{2+}$, and $Mn^{2+}$, stimulated the enzyme activity in both the cleavage and synthesis directions, and the enzyme was very sensitive to inhibition by $HgCl_2$ and $CuSO_4$.

• Journal of Applied Biological Chemistry
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• 제43권1호
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• pp.5-11
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• 2000

Three cDNA clones encoding rice calmodulin (CaM) isoforms (OsCaM-1, OsCaM-2, and OsCaM-3) were isolated from a rice cDNA library constructed from suspension-cultured rice cells treated with fungal elicitor. The coding regions of OsCaM-1 and O.sCaM-2 were 89% homologous at DNA Ievel, whereas the 5' and 3' untranslated regions were highly divergent. The polypeptides encoded by OsCaM-1 and OsCaM-2 was identical except two conservative substitution at position 8 and 75. The coding region of OsCaM-3 was consist of a typical conserved CaM domain and an additional C-terminal extension. The amino acid sequence of conserved CaM domain of OsCaM-3 shared only 86% identity with that OsCaM-1. The OsCaM-3 cDNA is belongs to a novel group of calmodulin gene due to its C-terminal extension of 38 amino acids, a large number of which are positively charged. The extension also contains a C-terminal CaaX-box prenylation site (CVlL). Genomic Southern analysis revealed at least six copies of CaM or CaM-related genes, suggesting that calmodulin may be represented by a small multigene family in the rice geneme. Expression of OsCaM gene was examined through Northern blot analysis. Transcript level of OsCaM-3 was increased by treatment with a fungal elicitor, whereas the OsCaM-1 and OsCaM-2 genes did not respond to the fungal elicitor. The expression of OsCaM-3 gene was remarkable inhibited in the rice cells treated with cyclosporine A, calcinurin inhibitor.

• 산업융합연구
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• 제13권4호
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• pp.11-28
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• 2015

A company have to grow constantly. If a company does not grow and stagnant, it will be finally out of the market. The contemporary companies fully make use of M&A to search for new growth engines. The reason of companies using M&A as a important tool of a business strategy is the fastest way to achieve technology power, market power, competitiveness. The form of M&A was that leading companies take over smaller companies or merger and acquisition between small companies in the middle of 2000. But now, Mega mergers between industry leading companies often occur and especially domestic of course M&A of foreign companies occurs actively. These days the boom of stock market and the big companies are pouring on sale by restructuring, privatization and the basis of low interest will make the M&A market continuously. In this study, I suggest a solution of actual human resources management by analyzing proven M&A cases and search for various problems of a gap in the leadership and communication in connection with integration of organization culture after M&A. First of all, I arrange the theoretical concept of the subject and analyze the key factors of the success M&A cases, lastly I suggested a HR strategy after M&A. After M&A, HR strategy is ; First, a company have to build a organization culture which is that merger company accommodate a excellent organizational characteristic of predecessor company with consideration of culture difference. Second, M&A must proceed to remove of anxiety about the future and employment stability by excellent leaderships. Third, organization integration after M&A is influenced by the level of integration for that reason it was verified that M&A have to make progress by communication of each 2 organizations.

• 한국수산과학회지
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• 제18권1호
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• pp.63-66
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• 1985

동해와 남해 동부연안에서 1983년 가을 중 식물플랑크톤이 함유한 클로로필-a 양을 세포의 크기 별로 구분하여 조사하였다. 1. 가을철 동해 해수중의 세포의 크기 $300{\mu}m$이하 전체의 식물플랑크톤이 함유한 클로로필-a 양은 $0.202{\sim}1.350mg/m^3$(평균과 표준편차는 $0.597{\pm}0.287\;mg/m^3$)이었다. 표층수중에 포함된 양이 심층수 50m층까지)에서의 양에 비해 약간 많았다. 그리고, 수표면 $1m^2$하 수주의 클로로필-a 양은 St.에 따라 큰 차이 없이 평균 $17.013\;mg/m^2$이었다. 2. 세포의 크기 $60{\mu}m$이하의 미세플랑크톤이 함유한 클로로필-a 양은 $0.100{\sim}0.855\;mg/m^3$(평균 및 표준편차는 $0.372{\pm}0.201\;mg/m^3$)로서 표층수에서의 양이 심층수에 비해 약간 많았다. 이를 미세플랑크톤이 전체 식물플랑크톤 현존량에 차지하는 율은 클로로필-a 양으로 $25.4{\sim}83.3\%$로써 평균 $62.2\%$이었고 이 율 역시 표층수에서 약간 높았다.

• 대한수학회보
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• 제59권4호
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• pp.917-928
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• 2022

Let R be a commutative Noetherian ring and I an ideal of R. In this paper, we study colocalization of generalized local homology modules. We intend to establish a dual case of local-global principle for the finiteness of generalized local cohomology modules. Let M be a finitely generated R-module and N a representable R-module. We introduce the notions of the representation dimension r^I(M, N) and artinianness dimension a^I(M, N) of M, N with respect to I by r^I(M, N) = inf{i ∈ ℕ₀ : H^I_i(M, N) is not representable} and a^I(M, N) = inf{i ∈ ℕ₀ : H^I_i(M, N) is not artinian} and we show that a^I(M, N) = r^I(M, N) = inf{r^IR_𝔭 (M_𝔭,𝔭N) : 𝔭 ∈ Spec(R)} ≥ inf{a^IR_𝔭 (M_𝔭,𝔭N) : 𝔭 ∈ Spec(R)}. Also, in the case where R is semi-local and N a semi discrete linearly compact R-module such that N/∩_t>0I^tN is artinian we prove that inf{i : H^I_i(M, N) is not minimax}=inf{r^IR_𝔭 (M_𝔭,𝔭N) : 𝔭 ∈ Spec(R)＼Max(R)}.

• 한국식품영양학회지
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• 제10권4호
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• pp.475-479
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• 1997

최소 배지에 여러 아미노산과 대사 산물을 첨가하여 혐기성 조건하에서 배양시킨 Serratia marcescens ATCC 25419 세포 추출무에서 prodigiosin의 생합성을 조사한 결과 아미노산과 대사 산물들은 prodigiosin 생합성을 대조군보다 50-80% 정도 감소시켰다. 글리옥실산은 1-3mM에서 prodigiosin의 생합성을 대조군보다 20-40% 정도 증가시켰고, 특히 5mM의 농도에서는 최대 122% 증가시켰으나, 20-30mM에서 prodigiosin의 생합성을 50-90% 정도 감소시켰다. 한편, 혐기성과 호기성 조건의 피루브산과 $\alpha$-케토부티르산은 호기성 조건의 글리옥실산과 함께 조사한 모든 농도(0.5-30mM)에서 prodigiosin이 생성되지 않았으며 또한, 혐기성 조건하에서 높은 농도(20mM 이상)의 글리옥실산은 S. marcescens의 성장을 현저하게 억제시켰다. 이러한 결과들로부터 글리옥실산은 피루브산과 $\alpha$-케토부티르산과는 다르게 낮은 농도(1-5mM)에서는 S. marcescens의 1, 2차 대사물질로 작용하여 prodigiosin 생합성을 증가시키지만, 높은 온도(20mM 이상)에서는 S. marcescens의 성장을 억제시켜 2차 대사물질인 prodigiosin의 생합성도 억제된다고 사료된다.

• 대한수학회보
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• 제61권1호
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• pp.1-12
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• 2024

In this paper, we introduce the notion of Gorenstein (m, n)-flat modules as an extension of (m, n)-flat left R-modules over a ring R, where m and n are two fixed positive integers. We demonstrate that the class of all Gorenstein (m, n)-flat modules forms a Kaplansky class and establish that (𝓖𝓕_m,n(R),𝓖𝓒_m,n(R)) constitutes a hereditary perfect cotorsion pair (where 𝓖𝓕_m,n(R) denotes the class of Gorenstein (m, n)-flat modules and 𝓖𝓒_m,n(R) refers to the class of Gorenstein (m, n)-cotorsion modules) over slightly (m, n)-coherent rings.

• 생명과학회지
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• 제28권2호
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• pp.148-152
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• 2018

지역 미세 환경의 패치는 식물의 공간적 분포에 일차적 요인이다. 식물의 공간적 양상을 결정한다는 귀무가설을 임의화 과정을 통해 검증하였다. 홀아비꽃대는 초본으로 홀아비꽃대과(Chloranthaceae) 홀아비꽃대속(Chloranthus)에 속한다. 홀아비꽃대의 공간적 양상을 여러 패치 지표로 분석하였고, 분산 지수에 따른 플롯 크기별 운집 분포, 균일분포, 공간적 상관관계를 분석하였다. 홀아비꽃대의 집단 밀도(D)는 0.356에서 2.270으로 평균은 1.527이었다. 아홉산 홀아비꽃대의 분산지표(C)는 작은 플롯($2m{\times}2m$, $2m{\times}4m$, $4m{\times}4m$, $4m{\times}8m$, $8m{\times}8m$, and $8m{\times}16m$)은 1보다 작았으며 큰 플롯($16m{\times}16m$ and $16m{\times}32m$)은 1보다 상회하였다. 따라서 홀아비꽃대의 운집지표(CI)는 작은 플롯에서 음의 값으로 균일한 분포를 이룬다. 큰 플롯의 운집지표는 양의 값으로 나타났으나 그 값은 높지 않았다. 평균 클라운딩($M^{\ast}$)과 패치지수(PAI)는 모든 플롯에서 양의 값을 보였다.