928 resultados para Environnement réel
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The environmcnl exerts an important inJuence on the pefirmance of space systems. A brief rel'iew of mo.s/ of the studies, pre.~ented over the past eightem years, relating to the influence ar7d the possible utilization of thc solar radiation pressure &d aero&namic forces, with particular reference to attitude dynamics and control qf satellites is presented here. The semi-passive stabilizers employing rhese forces show p~qmise of long life, low power and economic sjsfems, which though slower in response, compare we1I wit11 the octiw coi~trollers. It is felt that mud more attention is necessary to the actual implema~tution of these ideas and devices: some of which me quite ingenious und unique.
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On introduit une nouvelle classe de schémas de renforcement des automates d'apprentissage utilisant les estimations des caractéristiques aléatoires de l'environnement. On montre que les algorithmes convergent en probabilité vers le choix optimal des actions. On présente les résultats de simulation et on suggère des applications à un environnement à plusieurs apprentissages
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In the noninfectious soil saprophyte Mycobacterium smegmatis, intracellular levels of the stress alarmones guanosine tetraphosphate and guanosine pentaphosphate, together termed (p)ppGpp, are regulated by the enzyme Rel(Msm). This enzyme consists of a single, bifunctional polypeptide chain that is capable of both synthesizing and hydrolyzing (p)ppGpp. The rel(Msm), knockout strain of M. smegmatis (Delta rel(Msm)) is expected to show a (p)ppGpp null (p)ppGpp(0)] phenotype. Contrary to this expectation, the strain is capable of synthesizing (p)ppGpp in vivo. In this study, we identify and functionally characterize the open reading frame (ORF), MSMEG_5849, that encodes a second functional (p)ppGpp synthetase in M. smegmatis. In addition to (p)ppGpp synthesis, the 567-amino-acid-long protein encoded by this gene is capable of hydrolyzing RNA(.)DNA hybrids and bears similarity to the conventional RNase HII enzymes. We have classified this protein as actRel(Msm) in accordance with the recent nomenclature proposed and have named it MS_RHII-RSD, indicating the two enzymatic activities present RHII, RNase HII domain, originally identified as (d) under bar omain of (u) under bar nknown (f) under bar unction 429 (DUF429), and RSD, RelA_SpoT nucleotidyl transferase domain, the SYNTH domain responsible for (p)ppGpp synthesis activity]. MS_RHII-RSD is expressed and is constitutively active in vivo and behaves like a monofunctional (p)ppGpp synthetase in vitro. The occurrence of the RNase HII and (p)ppGpp synthetase domains together on the same polypeptide chain is suggestive of an in vivo role for this novel protein as a link connecting the essential life processes of DNA replication, repair, and transcription to the highly conserved stress survival pathway, the stringent response.
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The molecular mechanism of antimony-resistant Leishmania donovani ((SbLD)-L-R)-driven up-regulation of IL-10 and multidrug-resistant protein 1 (MDR1) in infected macrophages (M phi s) has been investigated. This study showed that both promastigote and amastigote forms of (SbLD)-L-R, but not the antimony-sensitive form of LD, express a unique glycan with N-acetylgalactosamine as a terminal sugar. Removal of it either by enzyme treatment or by knocking down the relevant enzyme, galactosyltransferase in (SbLD)-L-R (KD (SbLD)-L-R), compromises the ability to induce the above effects. Infection of M phi s with KD (SbLD)-L-R enhanced the sensitivity toward antimonials compared with infection with (SbLD)-L-R, and infection of BALB/c mice with KD (SbLD)-L-R caused significantly less organ parasite burden compared with infection induced by (SbLD)-L-R. The innate immune receptor, Toll-like receptor 2/6 heterodimer, is exploited by (SbLD)-L-R to activate ERK and nuclear translocation of NF-kappa B involving p50/c-Rel leading to IL-10 induction, whereas MDR1 up-regulation is mediated by PI3K/Akt and the JNK pathway. Interestingly both recombinant IL-10 and (SbLD)-L-R up-regulate MDR1 in M. with different time kinetics, where phosphorylation of PI3K was noted at 12 h and 48 h, respectively, but M phi s derived from IL-10(-/-) mice are unable to show MDR1 up-regulation on infection with (SbLD)-L-R. Thus, it is very likely that an IL-10 surge is a prerequisite for MDR1 up-regulation. The transcription factor important for IL-10-driven MDR1 up-regulation is c-Fos/c-Jun and not NF-kappa B, as evident from studies with pharmacological inhibitors and promoter mapping with deletion constructs.
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The bacterial second messengers (p)ppGpp and bis-(3'-5')-cyclic dimeric GMP (c-di-GMP) regulate important functions, such as transcription, virulence, biofilm formation, and quorum sensing. In mycobacteria, they regulate long-term survival during starvation, pathogenicity, and dormancy. Recently, a Pseudomonas aeruginosa strain lacking (p) ppGpp was shown to be sensitive to multiple classes of antibiotics and defective in biofilm formation. We were interested to find out whether Mycobacterium smegmatis strains lacking the gene for either (p)ppGpp synthesis (Delta rel(Msm)) or c-di-GMP synthesis (Delta dcpA) would display similar phenotypes. We used phenotype microarray technology to compare the growth of the wild-type and the knockout strains in the presence of several antibiotics. Surprisingly, the Delta rel(Msm) and Delta dcpA strains showed enhanced survival in the presence of many antibiotics, but they were defective in biofilm formation. These strains also displayed altered surface properties, like impaired sliding motility, rough colony morphology, and increased aggregation in liquid cultures. Biofilm formation and surface properties are associated with the presence of glycopeptidolipids (GPLs) in the cell walls of M. smegmatis. Thin-layer chromatography analysis of various cell wall fractions revealed that the levels of GPLs and polar lipids were reduced in the knockout strains. As a result, the cell walls of the knockout strains were significantly more hydrophobic than those of the wild type and the complemented strains. We hypothesize that reduced levels of GPLs and polar lipids may contribute to the antibiotic resistance shown by the knockout strains. Altogether, our data suggest that (p)ppGpp and c-di-GMP may be involved in the metabolism of glycopeptidolipids and polar lipids in M. smegmatis.
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The alarmone (p)ppGpp regulates transcription, translation, replication, virulence, lipid synthesis, antibiotic sensitivity, biofilm formation, and other functions in bacteria. Signaling nucleotide cyclic di-GMP (c-di-GMP) regulates biofilm formation, motility, virulence, the cell cycle, and other functions. In Mycobacterium smegmatis, both (p) ppGpp and c-di-GMP are synthesized and degraded by bifunctional proteins Rel(Msm) and DcpA, encoded by rel(Msm) and dcpA genes, respectively. We have previously shown that the Delta rel(Msm) and Delta dcpA knockout strains are antibiotic resistant and defective in biofilm formation, show altered cell surface properties, and have reduced levels of glycopeptidolipids and polar lipids in their cell wall (K. R. Gupta, S. Kasetty, and D. Chatterji, Appl Environ Microbiol 81:2571-2578, 2015, http://dx.doi.org/10.1128/AEM.03999-14). In this work, we have explored the phenotypes that are affected by both (p) ppGpp and c-di-GMP in mycobacteria. We have shown that both (p) ppGpp and c-di-GMP are needed to maintain the proper growth rate under stress conditions such as carbon deprivation and cold shock. Scanning electron microscopy showed that low levels of these second messengers result in elongated cells, while high levels reduce the cell length and embed the cells in a biofilm-like matrix. Fluorescence microscopy revealed that the elongated Delta rel(Msm) and Delta dcpA cells are multinucleate, while transmission electron microscopy showed that the elongated cells are multiseptate. Gene expression analysis also showed that genes belonging to functional categories such as virulence, detoxification, lipid metabolism, and cell-wall-related processes were differentially expressed. Our results suggests that both (p) ppGpp and c-di-GMP affect some common phenotypes in M. smegmatis, thus raising a possibility of cross talk between these two second messengers in mycobacteria. IMPORTANCE Our work has expanded the horizon of (p) ppGpp and c-di-GMP signaling in Gram-positive bacteria. We have come across a novel observation that M. smegmatis needs (p) ppGpp and c-di-GMP for cold tolerance. We had previously shown that the Delta rel(Msm) and Delta dcpA strains are defective in biofilm formation. In this work, the overproduction of (p) ppGpp and c-di-GMP encased M. smegmatis in a biofilm-like matrix, which shows that both (p) ppGpp and c-di-GMP are needed for biofilm formation. The regulation of cell length and cell division by (p) ppGpp was known in mycobacteria, but our work shows that c-di-GMP also affects the cell size and cell division in mycobacteria. This is perhaps the first report of c-di-GMP regulating cell division in mycobacteria.
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State-of-the-art large vocabulary continuous speech recognition (LVCSR) systems often combine outputs from multiple subsystems developed at different sites. Cross system adaptation can be used as an alternative to direct hypothesis level combination schemes such as ROVER. In normal cross adaptation it is assumed that useful diversity among systems exists only at acoustic level. However, complimentary features among complex LVCSR systems also manifest themselves in other layers of modelling hierarchy, e.g., subword and word level. It is thus interesting to also cross adapt language models (LM) to capture them. In this paper cross adaptation of multi-level LMs modelling both syllable and word sequences was investigated to improve LVCSR system combination. Significant error rate gains up to 6.7% rel. were obtained over ROVER and acoustic model only cross adaptation when combining 13 Chinese LVCSR subsystems used in the 2010 DARPA GALE evaluation. © 2010 ISCA.
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目录
Resumo:
本书阐明了板壳断裂理论的基础。论证了Reissner型板壳断裂理论的科学性、经典板壳断裂理论的缺陷及在一定范围内仍具有的实用价值;介绍了作者所创意的研究Reissner型板壳断裂纹尖端场的方法等。
目录
- §1.1 板壳弯曲断裂问题
- §1.2 Kirchhoff经典板壳弯曲断裂理论
- §1.3 Reissner型板壳弯曲断裂理论
- §1.4 Kirchhoff与Reissner型板壳弯曲断裂理论的比较
- §1.5 含裂纹有限尺寸板壳断裂分析的局部-整体法
- §1.6 含表面裂纹板壳
- §2.1 Kirchhoff板的基本概念和基本假定
- §2.2 基本公式与弹性曲面微分方程
- §2.3 边界条件
- §2.4 弹性薄板的应变能
- §2.5 极坐标下的挠曲面微分方程与内力公式
- §2.6 裂纹尖端场特征展开式通项公式
- §2.7 Kirchhoff板弯曲应力强度因子
- §3.1 基本方程和公式的复变函数表示
- §3.2 所引入函数的确定程度与一般形式
- §3.3 坐标变换与边界条件
- §3.4 运用保角变换方法求解孔口问题
- §3.5 应力强度因子与函数Φ(z)的关系
- §3.6 复变-主部分析法之应用简例
- §3.7 共直线裂纹问题的一般解答
- §3.8 典型弯曲裂纹问题的解答及弯曲应力强度因子公式
- §3.9 共圆曲线裂纹问题的解答及弯曲应力强度因子公式
- §4.1 裂纹尖端奇异元的位移模式与弯曲应力强度因子
- §4.2 裂纹尖端奇异元的刚度矩阵
- §4.3 裂纹尖端奇异元与常规单元的连接
- §4.4 解析法与数值法的结果比较与讨论
- §4.5 两共线半无限裂纹问题的定解条件及解的实用价值
- §5.1 Reissner型板的基本假定
- §5.2 Reissner型板的基本公式与平衡微分方程
- §5.3 基本方程的简化
- §5.4 边界条件
- §5.5 极坐标下的基本公式与平衡微分方程
- §5.6 两种平板理论用于无裂纹板时的比较
- §5.7 两种乎板理论用于含裂纹板时的比较
- §6.1 基本方程和一般求解方法
- §9.1 局部-整体法与其它解析和数值法的结果比较
- §9.2 边界对应力强度因子的影响
- §9.3 板的支承条件及长宽比的影响
- §9.5 计算Reissner型板应力强度因子的一组近似方程与近似解法
- §9.4 Reissner型板理论与Kirchhoff板理论所得应力强度因子的比较
- §9.6 关于数值计算的几点讨论
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目录
- 访罗湖 忆当年[李佩]
- 怀念同窗益友郭永怀教授[钱伟长]
- 郭永怀追求科学、为国献身的一生[洪友士]
- 深深怀念为核盾牌献身的著名科学家--郭永怀先生 中国工程物理研究院
- 深切怀念郭永怀教授的奠基性贡献 中国空气动力研究与发展中心
- 胸怀长江长城 心系国家安危--纪念我国核防护工程奠基人郭永怀先生[周丰峻]
- 缅怀我们的首任系主任--郭永怀教授[辛厚文 马兴孝 俞书勤 何天敬]
- 科学和技术结合的典范--纪念郭永怀先生诞辰九十周年[郑哲敏 李家春]
- 怀念与感激[俞鸿儒]
- 继承先师遗愿,谈我所冲击动力学的发展--纪念郭永怀副院长诞辰九十周年[陈裕泽]
- 英名长存--纪念郭永怀副院长诞辰九十周年[沈中毅]
- 郭永怀与我国导弹弹头再入气动物理研究[魏叔如]
- 科研工作引路人--纪念郭永怀九十诞辰[胡在军]
- 科技楷模,引路良师--怀念敬爱的郭永怀副院长[朱竟洪 郑百瑛]
- 七律 永怀永怀郭老师[董务民]
- 留得春晖映核魂--怀念我们的好领导好老师郭永怀同志[孙德纶 张克才]
- 难以忘怀--忆郭永怀副院长事迹点滴[孙天雄]
- 研究工作与工程技术工作之间的关系[谈庆明]
- 忆敬爱的郭永怀老师[张兆顺 呼和敖德]
- 根深叶茂 厚积薄发--追忆恩师郭永怀先生教诲我打好基础[严宗毅]
- 力学前辈,科德风范[徐友钜]
- 领导的楷模 学者的典范 青年的导师--怀念郭永怀副院长[于长勤]
- 怀念郭永怀副院长[陈裕泽]
- 关于郭永怀事迹的回顾[张长富]
- 严谨的导师,可亲的长者--忆著名的空气动力学家郭永怀先生[吴兰春]
- 严谨细致 实事求是--纪念郭永怀九十诞辰[李启廉]
- 纪念核武器环境试验技术的奠基人--郭永怀副院长诞辰九十周年[李荣林]
- 郭老精神激励着材料科学研究的不断深入[周维宣 谭云]
- 郭永怀副院长的关怀与我所有机材料研究的发展[陈晓丽]
- 忆与郭永怀副院长的一次谈话[孙德纶]
- 缅怀郭永怀院士[陈家镛]
- 记郭永怀先生二三事[屠善澄]
- Remembering Yunghuai Kuo[C.C.Lin]
- Recall with love and respect[William R.Sears]
- Y.H.Kuo:An appreciation[Frank E.Marble]
- A commemorative tribute to Professor Guo Yonghuai[T.Y.Wu]
- Y.H.Kuo:A great scientist,revered teacher and good friend[Alfred Ritter]
- 氢氧燃烧及爆轰驱动激波管[俞鸿儒]
- 颗粒材料中致密波结构研究[孙锦山 朱建士 贾祥瑞]
- 网格与高精度差分计算问题[张涵信 呙超 宗文刚]
- 植被层湍流的大涡模拟[李家春 谢正桐]
- 半浮区液桥热毛细振荡流[唐泽眉 阿燕 胡文瑞]
- 再入湍流尾迹及其对雷达散射的影响研究[牛家玉 于明]
- 超声射流中CS2分子态分辨转动弛豫研究[陈从香 刘世林 戴静华 张志萍 马兴孝]
- 37mm冲压加速器实验和计算[柳森 简和祥 白智勇 平新红 部绍清]
- 化学体系中噪声诱导的时空有序结构和随机共振[辛厚文 侯中怀 杨灵法]
- 根据守恒律计算热流和摩阻的有限元提法[童秉纲 段占元]
- 高阶精度线性耗散紧致格式的渐近稳定性[邓小刚 毛枚良]
- 离散流体力学:理论和数值方法[高智]
- 2号复合离心机自动控制系统研制[王磊 林明 冯晓军]
- 海沧大桥气动弹性特性风洞试验研究[李明水 陈忻 张大康 王卫华]
- 内爆炸载荷下圆管变形、损伤和破坏规律的研究[李永池 李大红 魏志刚 孙宇新]
- 两种凝聚炸药的静态断裂性能实验研究[罗景润 韦日演 马丽莲]
- 圆柱体侵彻薄靶极限击穿速度估算探讨[吴应白 唐平]
- 动力学修改方法在夹具设计中的应用研究[蒲怀强 唐定勇]
- Numerical simulation of non-linear stability of two-dimensional supersonic boundary layer[Shen Qing Yuan Xiangjiang]
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目录
- 1.1 化合物的生成焓,反应焓及燃烧热
- 1.2 热化学定律
- 1.3 热力学平衡与自由能,化学平衡与反应自由能
- 1.4 质量作用定律及可逆反应的平衡常数
- 1.5 平衡常数和标准反应自由能的关系
- 1.6 温度和压力对平衡常数的影响
- 1.7 绝热火焰温度计算
- 1.8 化学动力学中采用的几个基本概念和定义
- 1.9 反应的分类
- 1.10 阿累尼乌斯(Arrhenius)定律
- 1.11 双分子反应碰撞理论
- 1.12 反应分子数及反应级数
- 1.13 影响化学反应的因素
- 1.14 链锁反应
- 5.1 燃烧波的两种形式――缓燃(或火焰正常传播)及爆震
- 5.3 马兰特和利-恰及利耶的简化分析法
- 5.4 层流火焰传播速度的无量纲分析法
- 5.5 泽尔多维奇和弗朗克-卡门涅茨基的分区近似解
- 5.6 分区近似解的改进
- 5.7 精确解
- 5.8 物理化学参数对S1的影响及对火焰厚度的影响
- 5.9 火焰传播界限
- 5.10 用层流火焰传播速度计算化学动力参数的方法
- 5.11 火焰的基本性质及火焰的几何学
- 5.12 本生灯火焰稳定的条件
- 5.13 层流火焰传播速度的实验测定
- 5.14 单组元燃料滴燃烧
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