首页> 美国卫生研究院文献>Journal of Bacteriology >Constitutive activation of the fucAO operon and silencing of the divergently transcribed fucPIK operon by an IS5 element in Escherichia coli mutants selected for growth on L-12-propanediol.
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Constitutive activation of the fucAO operon and silencing of the divergently transcribed fucPIK operon by an IS5 element in Escherichia coli mutants selected for growth on L-12-propanediol.

机译:在被选为在L-112-丙二醇上生长的大肠杆菌突变体中通过IS5元件对fucAO操纵子进行组成性激活并使发散转录的fucPIK操纵子沉默。

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摘要

L-1,2-Propanediol is an irretrievable end product of L-fucose fermentation by Escherichia coli. Selection for increased aerobic growth rate on propanediol results in the escalation of basal synthesis of the NAD+-linked oxidoreductase encoded by fucO, a member of the fuc regulon for the utilization of L-fucose. In general, when fucO becomes constitutively expressed, two other simultaneous changes occur: the fucA gene encoding fuculose-1-phosphate aldolase becomes constitutively expressed and the fucPIK operon encoding fucose permease, fucose isomerase, and fuculose kinase becomes noninducible. In the present study, we show that fucO and fucA form an operon which is divergently transcribed from the adjacent fucPIK operon. In propanediol-positive and fucose-negative mutants the cis-controlling region shared by the operons fucAO and fucPIK is lengthened by 1.2 kilobases. DNA hybridization identified the insertion element to be IS5. This element, always oriented in the same direction with the left end (the BglII end) proximal to fucA, apparently causes constitutive expression of fucAO and noninducibility of fucPIK. The DNA of the fucAO operon and a part of the adjacent fucP was sequenced.
机译:L-1,2-丙二醇是大肠杆菌进行L-岩藻糖发酵的不可回收的终产物。选择提高丙二醇的有氧生长速率会导致由fucO编码的NAD +-连接的氧化还原酶的基础合成逐步升级,所述fucO是利用L-岩藻糖的fuc调节子的成员。通常,当fucO组成性表达时,会发生两个其他同时的变化:组成1型岩藻糖磷酸醛缩酶的fucA基因组成性表达,而编码岩藻糖通透酶,岩藻糖异构酶和岩藻糖激酶的fucPIK操纵子变为不可诱导的。在本研究中,我们显示fucO和fucA形成一个操纵子,该操纵子从相邻的fucPIK操纵子发散地转录。在丙二醇阳性和岩藻糖阴性突变体中,操纵子fucAO和fucPIK共有的顺式控制区延长了1.2个碱基。 DNA杂交确定插入元件为IS5。该元件的方向始终与fucA的左端(BglII端)近端方向相同,显然会导致fucAO的组成型表达和fucPIK的不可诱导性。对fucAO操纵子和一部分相邻fucP的DNA进行了测序。

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