乙酰化

Histone acetylation and deacetylation are crucial in the regulation of gene expression.

组蛋白乙酰化和去乙酰化对基因表达的调控至关重要，基因表达的动态变化将会影响染色质的结构。

The recent research shows that the process of acetylation and disacetylation is the key of regulating genes?activity.

最近的研究结果表明，核心组蛋白的乙酰化/去乙酰化过程是调控基因活性的一个关键步骤[1]。

Histone acetylation and deacetylation can regulate many chromosome functions, such as gene expression and chromosome segregation.

组蛋白乙酰化和去乙酰化可调节染色体的多种功能，例如基因表达和染色体分离等。

Except heptanoyl chitin, four of them,i.e.acetyl chitin,propionyl chitin,butyryl chitin and hexanoyl chitin,had high degree of substitution(from 1.5 to 2.0)and exhibited lyotropic liquid crystalline behavior and cholesteric phase.

文摘：四种羧酰化甲壳素即乙酰化、丙酰化、丁酰化和己酰化甲壳素在二氯乙酸溶液中均呈现胆甾型溶致液晶相。

This study was based on the soy protein isolates as raw materials. Chemical modification( acetylation,succinylation ,phosphorylation and urea modification) of SPI were used to improve adhesive strength and water resistance of SPI-based plywood adhesives. Then two modified ways combined were applied to SPI and their adhesive properties were studied. This research also characterized the thermal and adhesive properties of two major soy protein components 7S conglycinin and 11S glycinin after urea modification. Finally, the mechanism of improving SPI's adhesive properties was preliminarily discussed.

本文是以大豆分离蛋白为原料，进行SPI的化学修饰以提高其胶粘特性；采用了磷酸化试剂三聚磷酸钠、乙酰化试剂乙酸酐、琥珀酰化试剂琥珀酸酐和有机溶剂尿素修饰和变性SPI，研究修饰和变性后的SPI作为木材胶粘剂的胶粘性与耐水性，同时研究了两种方法复合修饰SPI对其粘度、胶粘强度和耐水性的影响；然后以SPI为原料，进行7S和11S球蛋白的提取以及胶粘特性的研究，对SPI起胶粘特性的机理进行了初步探讨。

Synthesizc 2-methyl-5-acetamino benzene sulfochloride using p-toluidine primer reactant by aceylation and chlorosulfonation.

以对甲基苯胺为起始原料，通过乙酰化和氯磺化反应合成2-甲基－5-乙酰氨基苯磺酰氯。

The optimal derivatization condition is reducting reaction 2.5h at 50℃followed by acetylating 2.5h at 90℃.

总结出了单糖衍生化最佳的反应条件为还原温度50℃、还原时间2.5h；乙酰化温度90℃、乙酰化时间2.5h。

Three methodsconventional direct acylation,acylation by phase transfer catalyst(PTC,and ionexchange-acylation were selected for the purpose of acetylating κ-carrageenan with 30kDa molecular weight.

选择常规直接酰化、相转移催化酰化和离子交换-酰化共3种方法对3万中等分子量的κ-卡拉胶进行了乙酰化反应。

"Acetylating H3K4 and demethylating H3K9 can actiate a gene; deacetylating H3K4 and methylating H3K9 can silence it," Karpen explains."Multiply modified at arious locations, these histones are a major factor in changing the functions of chromatin, independent of DNA sequence."

&H3K4的乙酰化和H3K9的去甲基化使基因活化；而H3K4去乙酰化和H3K9的甲基化则使基因沉默，& Karpen讲解道，&组蛋白的多部位多重调节是改变染色质功能的主要因素，并与DNA的序列无关&

Methods After treated with a specific demethylating agent,Aza and acetylating agent, TSA, the status of 5'CpC island methylation of ING1b gene in HT29 human colon cancer cell line was analyzed using methylation specific polymerase chain reaction,and the level of histone acetylation was analyzed by chromatin immunoprecipitation,and reverse transcription polymerase chain reactionwas used to examine ING1b mRNA expression.

应用特异性DNA甲基转移酶抑制剂5-氮-2'-脱氧胞苷（5-Aza-2'-dc，以下简称Aza）及组蛋白去乙酰化酶抑制剂曲古抑菌素A作用人结肠癌细胞株HT29后，用甲基化特异性PCR检测该ING1b基因核心启动子区域CpG岛甲基化情况，用染色质免疫沉淀检测其乙酰化组蛋白绑定的DNA情况，并用逆转录聚合酶链反应检测ING1bmRNA表达。

This one mode pays close attention to network credence foundation of the businessman very much.

这一模式非常关注商人的网络信用基础。

Cell morphology of bacterial ghost of Pasteurella multocida was observed by scanning electron microscopy and inactivation ratio was estimated by CFU analysi.

扫描电镜观察多杀性巴氏杆菌细菌幽灵和菌落形成单位评价遗传灭活率。