首页> 外文期刊>Journal of bacteriology >BetS Is a Major Glycine Betaine/Proline Betaine Transporter Required for Early Osmotic Adjustment in Sinorhizobium meliloti
【24h】

BetS Is a Major Glycine Betaine/Proline Betaine Transporter Required for Early Osmotic Adjustment in Sinorhizobium meliloti

机译:BetS是主要的甘氨酸甜菜碱/脯氨酸甜菜碱转运蛋白,需要对苜蓿中华根瘤菌进行早期渗透调节

获取原文
           

摘要

Hybridization to a PCR product derived from conserved betaine choline carnitine transporter (BCCT) sequences led to the identification of a 3.4-kb Sinorhizobium meliloti DNA segment encoding a protein (BetS) that displays significant sequence identities to the choline transporter BetT of Escherichia coli (34%) and to the glycine betaine transporter OpuD of Bacillus subtilis (30%). Although the BetS protein shows a common structure with BCCT systems, it possesses an unusually long hydrophilic C-terminal extension (169 amino acids). After heterologous expression of betS in E. coli mutant strain MKH13, which lacks choline, glycine betaine, and proline transport systems, both glycine betaine and proline betaine uptake were restored, but only in cells grown at high osmolarity or subjected to a sudden osmotic upshock. Competition experiments demonstrated that choline, ectoine, carnitine, and proline were not effective competitors for BetS-mediated betaine transport. Kinetic analysis revealed that BetS has a high affinity for betaines, with Kms of 16 ± 2 μM and 56 ± 6 μM for glycine betaine and proline betaine, respectively, in cells grown in minimal medium with 0.3 M NaCl. BetS activity appears to be Na+ driven. In an S. meliloti betS mutant, glycine betaine and proline betaine uptake was reduced by about 60%, suggesting that BetS represents a major component of the overall betaine uptake activities in response to salt stress. β-Galactosidase activities of a betS-lacZ strain grown in various conditions showed that betS is constitutively expressed. Osmotic upshock experiments performed with wild-type and betS mutant cells, treated or not with chloramphenicol, indicated that BetS-mediated betaine uptake is the consequence of immediate activation of existing proteins by high osmolarity, most likely through posttranslational activation. Growth experiments underscored the crucial role of BetS as an emerging system involved in the rapid acquisition of betaines by S. meliloti subjected to osmotic upshock.
机译:与保守甜菜碱胆碱肉碱转运蛋白(BCCT)序列衍生的PCR产物的杂交导致鉴定了一个3.4 kb的 Sinorhizobium meliloti DNA片段,该片段编码的蛋白(BetS)与胆碱具有明显的序列同一性大肠杆菌(em)的BetT转运蛋白(34%)和枯草芽孢杆菌(em)的甘氨酸甜菜碱转运蛋白OpuD(30%)。尽管BetS蛋白在BCCT系统中显示出共同的结构,但它具有异常长的亲水性C端延伸(169个氨基酸)。 betS E中异源表达后。缺乏胆碱,甘氨酸甜菜碱和脯氨酸转运系统的大肠杆菌突变株MKH13,甘氨酸甜菜碱和脯氨酸甜菜碱的摄取均得以恢复,但仅在高渗透压下生长或遭受突然的渗透升冲击的细胞中得以恢复。竞争实验表明,胆碱,植物素,肉碱和脯氨酸不是BetS介导的甜菜碱运输的有效竞争者。动力学分析表明,BetS对甜菜碱具有很高的亲和力,其中甜菜碱和脯氨酸甜菜碱的 K m s分别为16±2μM和56±6μM。细胞在含0.3 M NaCl的基本培养基中生长。 BetS活性似乎是Na + 驱动的。在 S中。 meliloti betS 突变体的甘氨酸甜菜碱和脯氨酸甜菜碱吸收减少了约60%,这表明BetS代表了整体甜菜碱吸收活动的主要组成部分,以应对盐胁迫。在不同条件下生长的 betS-lacZ 菌株的β-半乳糖苷酶活性表明 betS 是组成型表达的。在野生型和 betS 突变细胞中进行渗透渗透实验,无论是否用氯霉素处理,表明BetS介导的甜菜碱摄取是高渗透压立即激活现有蛋白质的结果,很可能是通过翻译后激活。生长实验强调了BetS作为新兴系统的重要作用,该系统涉及 S快速获得甜菜碱。 meliloti 遭受渗透性冲击。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号