恶臭假单胞菌BS3701石油组分降解菌株MBL-fold金属水解酶超家族蛋白编码基因分析

Q4 Medicine
I. Pozdnyakova-Filatova, A. A. Zagoskin, M. Zakharova, M. Nagornykh
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引用次数: 0

摘要

目标。确定产物被标注为“MBL-fold金属水解酶超家族”的基因是否与金属β-内酰胺酶组蛋白相关。材料与方法。利用ClustalW、IQ-TREE、iTOL等资源对标记为“MBL-fold金属水解酶超家族”的7个基因序列进行分析。利用Primer-BLAST资源选择实时PCR所需的寡核苷酸。实时荧光定量PCR检测基因表达水平。用头孢吡肟和美罗培南测定MIC和MBC。结果对所研究基因的核苷酸序列分析表明,这些基因均不包含在含有金属β-内酰胺酶序列的支系中。在指数生长阶段,发现了与所研究蛋白相对应的mrna。MIC和MBC检测显示β-内酰胺酶组对抗生素的耐药水平较低。恶臭假单胞菌bs3701株MBL表型检测为阴性。所研究的基因和相应的蛋白与金属β-内酰胺酶无关。它们与恶臭假单胞菌BS3701对金属β-内酰胺酶组抗生素的耐药性无关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Analysis of the genes encoding the MBL-fold metallohydrolase superfamily proteins of the Pseudomonas putida BS3701 petroleum component-degrading strain
Objective. To determine whether the genes whose products are annotated as «MBL-fold metallohydrolase superfamily» are related to the proteins of the metallo-β-lactamase group. Materials and Methods. Sequences of the 7 genes annotated as «MBL-fold metallohydrolase superfamily» were analyzed using the following resources: ClustalW, IQ-TREE, iTOL. Selection of the oligonucleotides for real-time PCR was performed using the Primer-BLAST resource. The level of gene expression was assessed using real-time PCR. MIC and MBC measuring was performed using cefepime and meropenem. The double-disc method with EDTA was used to determine the presence of MBL in the strain. Results. Analysis of the nucleotide sequences of the studied genes revealed that all of them were not included in the clade containing sequences of metallo-β-lactamase. In the exponential growth phase, mRNAs corresponding to the studied proteins were found. Determination of MIC and MBC revealed a low level of resistance to antibiotics of the β-lactamase group. The phenotypic test was negative for MBL in P. putida strain BS3701. Conclusions. The investigated genes and corresponding proteins are not related to metallo-β-lactamases. They are not involved in the resistance of P. putida BS3701 to antibiotics of the metallo-β-lactamase group.
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