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Erratum for Lori et al., “A Single-Domain Response Regulator Functions as an Integrating Hub To Coordinate General Stress Response and Development in Alphaproteobacteria”

机译:Lori等人的勘误,“单域响应调节剂作为整合轮毂发挥作用,以协调α变形杆菌的一般应激反应和发育”

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ERRATUM Volume 9, issue 3, e00809-18, 2018, https://doi.org/10.1128/mBio.00809-18 . We inadvertently referred to Asp53 as the phosphorylated residue in MrrA, instead of Asp58, in the main text (“MrrA is a central phosphorylation hub for multiple histidine kinases”) and in Fig.?S2 in the supplemental material. We also listed the wrong primers to construct this mutant version of MrrA. The primers originally listed were indeed for the Asp53Asn mutation, which however was not tested. The construct used and shown in our paper (Fig.?S2A) is the Asp58Asn (D58N) mutant version, and we verified this by resequencing the insert part of the plasmid. Accordingly, we have corrected Fig.?S2A and Table?S2?and they have been replaced online. These changes do not in any way affect the conclusions of the paper. We apologize to the readers for any confusion that may have arisen from our mistake.
机译:勘误表第9卷,第3期,e00809-18,2018,https://doi.org/10.1128/mBio.00809-18。在正文中(“ MrrA是多种组氨酸激酶的中央磷酸化中心”),在补充材料中,我们无意中将Asp53称为MrrA中的磷酸化残基,而不是Asp58。我们还列出了错误的引物,以构建MrrA的此突变版本。最初列出的引物确实是针对Asp53Asn突变的,但是未经测试。在我们的论文中使用和显示的构建体(图?S2A)是Asp58Asn(D58N)突变体,我们通过对质粒的插入部分重新测序来验证这一点。因此,我们更正了图S2A和表S2,并已在线替换它们。这些变化不会以任何方式影响本文的结论。对于因我们的错误而引起的任何困惑,我们深表歉意。

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