Hemamali Erandika H, Weerasinghe Laksiri P, Tanaka Hideaki, Kurisu Genji, Perera Inoka C
Synthetic Biology Laboratory, Department of Zoology and Environment Sciences, Faculty of Science, University of Colombo, Colombo, Sri Lanka.
Department of Chemistry, Faculty of Applied Science, University of Sri Jayewardenapura, Colombo, Sri Lanka.
Biodegradation. 2022 Apr;33(2):117-133. doi: 10.1007/s10532-021-09970-x. Epub 2022 Jan 6.
Application of genetically engineered bacterial strains for biodegradation of hydrocarbons is a sustainable solution for treating pollutants as well as in industrial applications. However, the process of bioengineering should be carefully carried out to optimize the output. Investigation of regulatory genes for bioengineering is essential for developing synthetic circuits for effective biocatalysts. Here we focus on LcaR, a putative transcriptional regulator affecting the expression of alkB2 and lcaR operon that has a high potential to become a tool in designing such pathways. Four LcaR dimers bind specifically to the upstream regulatory region where divergent promoters of alkB2 and lcaR genes are located with high affinity at a K of 0.94 ± 0.17 nM and a Hill coefficient is 1.7 ± 0.3 demonstrating cooperativity in the association. Ligand binding alters the conformation of LcaR, which releases the regulator from its cognate DNA. Tetradecanal and hexadecanal act as natural ligands of LcaR with an IC values of 3.96 ± 0.59 µg/ml and 0.68 ± 0.21 µg/ml, respectively. The structure and function of transcription factors homologous to LcaR have not been characterized to date. This study provides insight into regulatory mechanisms of alkane degradation with a direction towards potential applications in bioengineering for bioremediation and industrial applications.
应用基因工程细菌菌株进行碳氢化合物的生物降解,对于处理污染物以及工业应用而言,是一种可持续的解决方案。然而,生物工程过程应谨慎进行以优化产出。对生物工程调控基因的研究对于开发有效生物催化剂的合成电路至关重要。在此,我们聚焦于LcaR,一种假定的转录调节因子,它影响alkB2和lcaR操纵子的表达,极有可能成为设计此类途径的工具。四个LcaR二聚体特异性结合至alkB2和lcaR基因的分歧启动子所在的上游调控区域,结合亲和力高,解离常数K为0.94±0.17 nM,希尔系数为1.7±0.3,表明结合过程存在协同性。配体结合会改变LcaR的构象,使其从同源DNA上释放。十四醛和十六醛作为LcaR的天然配体,IC值分别为3.96±0.59 μg/ml和0.68±0.21 μg/ml。与LcaR同源的转录因子的结构和功能迄今尚未得到表征。本研究为烷烃降解的调控机制提供了见解,朝着生物修复和工业应用在生物工程中的潜在应用方向发展。