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首页> 外文期刊>Applied and Environmental Microbiology >Gene Expression Profiling of Listeria monocytogenes Strain F2365 during Growth in Ultrahigh-Temperature-Processed Skim Milk
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Gene Expression Profiling of Listeria monocytogenes Strain F2365 during Growth in Ultrahigh-Temperature-Processed Skim Milk

机译:李氏单核细胞增生李斯特氏菌菌株F2365在超高温加工脱脂乳中的生长过程中的基因表达谱

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To study how Listeria monocytogenes survives and grows in ultrahigh-temperature-processed (UHT) skim milk, microarray technology was used to monitor the gene expression profiles of strain F2365 in UHT skim milk. Total RNA was isolated from strain F2365 in UHT skim milk after 24 h of growth at 4°C, labeled with fluorescent dyes, and hybridized to “custom-made” commercial oligonucleotide (35-mers) microarray chips containing the whole genome of L. monocytogenes strain F2365. Compared to L. monocytogenes grown in brain heart infusion (BHI) broth for 24 h at 4°C, 26 genes were upregulated (more-than-twofold increase) in UHT skim milk, whereas 14 genes were downregulated (less-than-twofold decrease). The upregulated genes included genes encoding transport and binding proteins, transcriptional regulators, proteins in amino acid biosynthesis and energy metabolism, protein synthesis, cell division, and hypothetical proteins. The downregulated genes included genes that encode transport and binding proteins, protein synthesis, cellular processes, cell envelope, energy metabolism, a transcriptional regulator, and an unknown protein. The gene expression changes determined by microarray assays were confirmed by real-time reverse transcriptase PCR analyses. Furthermore, cells grown in UHT skim milk displayed the same sensitivity to hydrogen peroxide as cells grown in BHI, demonstrating that the elevated levels of expression of genes encoding manganese transporter complexes in UHT skim milk did not result in changes in the oxidative stress sensitivity. To our knowledge, this report represents a novel study of global transcriptional gene expression profiling of L. monocytogenes in a liquid food.
机译:为了研究单核细胞增生李斯特菌如何在超高温加工(UHT)脱脂乳中存活和生长,微阵列技术用于监测UHT脱脂乳中F2365菌株的基因表达谱。在4°C下生长24小时后,从UHT脱脂牛奶中的F2365菌株中分离总RNA,并用荧光染料标记,然后与包含L的整个基因组的“定制”商业寡核苷酸(35-聚体)微阵列芯片杂交。单核细胞增生病菌株F2365。与在4°C下在脑心浸液(BHI)肉汤中生长24小时的单核细胞增生李斯特菌相比,UHT脱脂奶中有26个基因被上调(增加了两倍以上),而14个基因被下调(了不到两倍)。减少)。上调的基因包括编码转运和结合蛋白,转录调节子,氨基酸生物合成和能量代谢中的蛋白,蛋白合成,细胞分裂和假定蛋白的基因。下调的基因包括编码转运和结合蛋白,蛋白合成,细胞过程,细胞包膜,能量代谢,转录调节子和未知蛋白的基因。通过实时逆转录酶PCR分析证实了通过微阵列测定法确定的基因表达变化。此外,在UHT脱脂奶中生长的细胞对过氧化氢的敏感性与在BHI中生长的细胞相同,这表明UHT脱脂奶中编码锰转运蛋白复合物的基因表达水平的升高不会导致氧化应激敏感性的变化。据我们所知,该报告代表了液态食品中单核细胞增生李斯特氏菌的全球转录基因表达谱的新颖研究。

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