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Nucleotide sequence and expression of cheF an essential gene for chemotaxis in Bacillus subtilis.

机译:cheF的核苷酸序列和表达cheF是枯草芽孢杆菌趋化性的必需基因。

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摘要

The cheF gene, which is involved in chemotaxis in Bacillus subtilis, has been cloned, expressed, and sequenced. This gene is contained in a 0.7-kilobase PstI DNA fragment that was isolated from a lambda Charon 4A B. subtilis chromosomal DNA library. This fragment was subcloned into the expression vector pSI-1 and shown to complement the cheF mutation both for chemotaxis and for methanol production in response to the addition of attractants. Plasmid-encoded DNA expression in B. subtilis maxicells indicated that a membrane-associated polypeptide of 20-kilodaltons was expressed from this 0.7-kilobase DNA. The nucleotide sequence of this DNA fragment was determined, and an open reading frame capable of encoding a putative 175-amino-acid protein (Mr 20,002) was identified. In an effort to understand the function of the cheF protein, the dosage of the cheF gene product was varied by altering the concentration of IPTG (isopropyl-beta-D-thiogalactopyranoside) during growth. In the presence of high concentrations of IPTG, chemotaxis was inhibited and methanol production was impaired.
机译:与枯草芽孢杆菌趋化性有关的cheF基因已被克隆,表达和测序。该基因包含在一个0.7碱基对的PstI DNA片段中,该片段是从λCharon 4A枯草芽孢杆菌染色体DNA文库中分离出来的。将该片段亚克隆到表达载体pSI-1中,并显示出对cheF突变的补充,以用于趋化性和响应于引诱剂的甲醇生产。枯草芽孢杆菌中质粒编码的DNA表达表明,从该0.7碱基碱基的DNA中表达了20公斤的膜相关多肽。确定该DNA片段的核苷酸序列,并鉴定出能够编码假定的175个氨基酸蛋白(Mr 20,002)的开放阅读框。为了理解cheF蛋白的功能,通过在生长过程中改变IPTG(异丙基-β-D-硫代吡喃半乳糖苷)的浓度来改变cheF基因产物的剂量。在高浓度IPTG的存在下,趋化作用受到抑制,甲醇的生成受到损害。

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