首页> 美国卫生研究院文献>Applied and Environmental Microbiology >Glyphosate Resistance as a Novel Select-Agent-Compliant Non-Antibiotic-Selectable Marker in Chromosomal Mutagenesis of the Essential Genes asd and dapB of Burkholderia pseudomallei
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Glyphosate Resistance as a Novel Select-Agent-Compliant Non-Antibiotic-Selectable Marker in Chromosomal Mutagenesis of the Essential Genes asd and dapB of Burkholderia pseudomallei

机译:草甘膦抗性作为拟南芥中必不可少的基本基因asd和dapB的染色体诱变中的一种新的选择剂兼容非抗生素选择标记。

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摘要

Genetic manipulation of the category B select agents Burkholderia pseudomallei and Burkholderia mallei has been stifled due to the lack of compliant selectable markers. Hence, there is a need for additional select-agent-compliant selectable markers. We engineered a selectable marker based on the gat gene (encoding glyphosate acetyltransferase), which confers resistance to the common herbicide glyphosate (GS). To show the ability of GS to inhibit bacterial growth, we determined the effective concentrations of GS against Escherichia coli and several Burkholderia species. Plasmids based on gat, flanked by unique flip recombination target (FRT) sequences, were constructed for allelic-replacement. Both allelic-replacement approaches, one using the counterselectable marker pheS and the gat-FRT cassette and one using the DNA incubation method with the gat-FRT cassette, were successfully utilized to create deletions in the asd and dapB genes of wild-type B. pseudomallei strains. The asd and dapB genes encode an aspartate-semialdehyde dehydrogenase (BPSS1704, chromosome 2) and dihydrodipicolinate reductase (BPSL2941, chromosome 1), respectively. Mutants unable to grow on media without diaminopimelate (DAP) and other amino acids of this pathway were PCR verified. These mutants displayed cellular morphologies consistent with the inability to cross-link peptidoglycan in the absence of DAP. The B. pseudomallei 1026b Δasd::gat-FRT mutant was complemented with the B. pseudomallei asd gene on a site-specific transposon, mini-Tn7-bar, by selecting for the bar gene (encoding bialaphos/PPT resistance) with PPT. We conclude that the gat gene is one of very few appropriate, effective, and beneficial compliant markers available for Burkholderia select-agent species. Together with the bar gene, the gat cassette will facilitate various genetic manipulations of Burkholderia select-agent species.
机译:由于缺乏顺应性的选择标记,已抑制了B类选择病原体Burkholderia pseudomallei和Mallkholderia mallei的遗传操作。因此,需要另外的符合选择剂的选择标记。我们设计了基于gat基因(编码草甘膦乙酰基转移酶)的选择标记,该标记赋予了对常见除草剂草甘膦(GS)的抗性。为了显示GS抑制细菌生长的能力,我们确定了针对大肠杆菌和几种伯克霍尔德氏菌的GS有效浓度。构建了以盖特为基础的质粒,侧翼是独特的翻转重组靶(FRT)序列,用于等位基因置换。两种等位基因置换方法(一种使用可逆选择标记pheS和gat-FRT盒的方法,一种使用DNA孵育方法与gat-FRT盒的方法)被成功地用于在野生型B的asd和dapB基因中创建缺失。假苹果毒株。 asd和dapB基因分别编码天冬氨酸-半醛脱氢酶(BPSS1704,染色体2)和二氢二吡啶甲酸酯还原酶(BPSL2941,染色体1)。 PCR验证了没有二氨基庚二酸酯(DAP)和该途径其他氨基酸无法在培养基上生长的突变体。这些突变体显示出细胞形态,与在没有DAP的情况下不能交联肽聚糖相一致。 B. pseudomallei 1026bΔ asd :: gat-FRT 突变体与 B互补。通过选择 bar 基因(编码),将位点特异转座子mini-Tn 7 - bar 上的拟假基因asd 基因编码耐Bialaphos / PPT)。我们得出的结论是, gat 基因是可用于 Burkholderia 选择剂物种的极少数适当,有效和有益的顺应性标记之一。与 bar 基因一起, gat 盒将促进 Burkholderia 选择剂物种的多种遗传操作。

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