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首页> 外文期刊>Analytical chemistry >CHARACTERIZATION OF PCR PRODUCTS FROM BACILLI USING ELECTROSPRAY IONIZATION FTICR MASS SPECTROMETRY
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CHARACTERIZATION OF PCR PRODUCTS FROM BACILLI USING ELECTROSPRAY IONIZATION FTICR MASS SPECTROMETRY

机译:电喷雾电离质谱法鉴定芽孢杆菌PCR产物

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A procedure for rapid purification of polymerase chain reaction (PCR) products allowing precise molecular weight determination using electrospray ionization-Fourier transform ion cyclotron resonance (ESI-FTICR) mass spectrometry is described, PCR amplification utilized the DNA polymerase from Pyrococcus furiosus (Pfu) which, unlike Tag, does not incorporate a nontemplated terminal deoxyadenosine phosphate, An 89-base pair nucleotide portion of the spacer region between the 16S and 23S ribosomal rRNA genes was amplified from the genome of three members of Bacillus cereus group and a 114 nucleotide region from the Bacillus subtilis, PCR involves polymerization of nucleotide precursors using two oligonucleotide primers and an amplification enzyme, as well as the presence of metal ions, Mass spectrometric analysis greatly benefits from removal of the oligonucleotide primers (15- and 17-mers in this instance) and nucleotide precursors since they adversely affect sensitivity and metal ion adduction results in an inaccurate molecular weight determination, In the presence of guanidinium hydrochloride, the PCR products bind preferentially to a silica resin, allowing removal of other components (i,e,, dNTP's, primers, and salts), Further removal of metal ions was accomplished using a microdialysis device, allowing samples to be pumped through a hollow cellulose fiber with an external countercurrent now of 2.5 mM ammonium acetate, Prior to injection into the mass spectrometer, the sample buffer was adjusted to 50 vol % acetonitrile, 25 mM piperidine, and 25 mM imidazole, which enhanced signal intensity, The molecular weights of the PCR products determined by nucleotide sequence and MS analysis were in excellent agreement, and several PCR products were analyzed where mass differences corresponding to single base substitutions could be accurately assigned, These assignments were possible due to the high mass precision, accuracy, and resolution FTICR inherently affords, This constitutes the first report demonstrating the ionization and detection of PCR products by mass spectrometry with mass precision and accuracy for assigment of such modifications or substitutions.
机译:描述了一种快速纯化聚合酶链反应(PCR)产物的方法,该方法可使用电喷雾电离-傅立叶变换离子回旋共振(ESI-FTICR)质谱技术精确测定分子量,PCR扩增利用了激烈热球菌(Pfu)的DNA聚合酶与Tag不同的是,它没有掺入非模板化的末端脱氧腺苷磷酸,从蜡状芽孢杆菌组的三个成员的基因组和一个来自蜡状芽孢杆菌的三个成员的基因组中扩增了16S和23S核糖体rRNA基因之间间隔区的89个碱基对的核苷酸部分。枯草芽孢杆菌,PCR涉及使用两个寡核苷酸引物和一个扩增酶聚合核苷酸前体,以及金属离子的存在,质谱分析极大地受益于去除了寡核苷酸引物(在这种情况下为15-和17-mers)和核苷酸前体,因为它们会对灵敏度和金属离子吸附产生不利影响还原导致分子量测定不准确。在盐酸胍存在下,PCR产物优先与二氧化硅树脂结合,从而允许去除其他组分(即dNTP,引物和盐),进一步去除金属离子通过使用微透析装置完成,允许样品通过中空纤维素纤维以2.5mM乙酸铵的外部逆流泵入。在注入质谱仪之前,将样品缓冲液调节至50 vol%乙腈,25 mM哌啶,和25 mM咪唑,它们增强了信号强度,通过核苷酸序列和MS分析确定的PCR产物的分子量非常吻合,并且分析了几种PCR产物,可以准确分配与单碱基取代相对应的质量差异,由于FTICR固有的高质量精度,准确性和分辨率,因此可以进行分配,滴定了第一个报告,证明了通过质谱进行电离和检测PCR产物的质量精确度和准确性,用于鉴定此类修饰或取代。

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