Nakano H, Takehara E, Nihira T, Yamada Y
Department of Biotechnology, Osaka University, Japan.
J Bacteriol. 1998 Jul;180(13):3317-22. doi: 10.1128/JB.180.13.3317-3322.1998.
Virginiae butanolides (VBs), which are among the butyrolactone autoregulators of Streptomyces species, act as a primary signal in Streptomyces virginiae to trigger virginiamycin biosynthesis and possess a specific binding protein, BarA. To clarify the in vivo function of BarA in the VB-mediated signal pathway that leads to virginiamycin biosynthesis, two barA mutant strains (strains NH1 and NH2) were created by homologous recombination. In strain NH1, an internal 99-bp EcoT14I fragment of barA was deleted, resulting in an in-frame deletion of 33 amino acid residues, including the second helix of the probable helix-turn-helix DNA-binding motif. With the same growth rate as wild-type S. virginiae on both solid and liquid media, strain NH1 showed no apparent changes in its morphological behavior, indicating that the VB-BarA pathway does not participate in morphological control in S. virginiae. In contrast, virginiamycin production started 6 h earlier in strain NH1 than in the wild-type strain, demonstrating for the first time that BarA is actively engaged in the control of virginiamycin production and implying that BarA acts as a repressor in virginiamycin biosynthesis. In strain NH2, an internal EcoNI-SmaI fragment of barA was replaced with a divergently oriented neomycin resistance gene cassette, resulting in the C-terminally truncated BarA retaining the intact helix-turn-helix motif. In strain NH2 and in a plasmid-integrated strain containing both intact and mutated barA genes, virginiamycin production was abolished irrespective of the presence of VB, suggesting that the mutated BarA retaining the intact DNA-binding motif was dominant over the wild-type BarA. These results further support the hypothesis that BarA works as a repressor in virginiamycin production and suggests that the helix-turn-helix motif is essential to its function. In strain NH1, VB production was also abolished, thus indicating that BarA is a pleiotropic regulatory protein controlling not only virginiamycin production but also autoregulator biosynthesis.
弗吉尼亚丁醇内酯(VBs)是链霉菌属丁内酯自调控因子之一,在弗吉尼亚链霉菌中作为触发维吉尼亚霉素生物合成的主要信号,并拥有一种特异性结合蛋白BarA。为阐明BarA在导致维吉尼亚霉素生物合成的VB介导信号通路中的体内功能,通过同源重组构建了两个barA突变菌株(NH1和NH2)。在NH1菌株中,barA的一个99bp内部EcoT14I片段被删除,导致33个氨基酸残基的框内缺失,包括可能的螺旋-转角-螺旋DNA结合基序的第二个螺旋。NH1菌株在固体和液体培养基上的生长速率与野生型弗吉尼亚链霉菌相同,其形态行为无明显变化,这表明VB-BarA通路不参与弗吉尼亚链霉菌的形态控制。相反,NH1菌株中维吉尼亚霉素的产生比野生型菌株提前6小时开始,首次证明BarA积极参与维吉尼亚霉素产生的控制,并暗示BarA在维吉尼亚霉素生物合成中起阻遏作用。在NH2菌株中,barA的一个内部EcoNI-SmaI片段被一个反向定向的新霉素抗性基因盒取代,导致C末端截短的BarA保留完整的螺旋-转角-螺旋基序。在NH2菌株以及含有完整和突变barA基因的质粒整合菌株中,无论是否存在VB,维吉尼亚霉素的产生均被消除,这表明保留完整DNA结合基序的突变BarA对野生型BarA具有显性作用。这些结果进一步支持了BarA在维吉尼亚霉素产生中起阻遏作用的假说,并表明螺旋-转角-螺旋基序对其功能至关重要。在NH1菌株中,VB的产生也被消除,因此表明BarA是一种多效调节蛋白,不仅控制维吉尼亚霉素的产生,还控制自调控因子的生物合成。