Xiong Liang-Bin, Sun Wan-Ju, Liu Yong-Jun, Wang Feng-Qing, Wei Dong-Zhi
State Key Laboratory of Bioreactor Engineering, Newworld Institute of Biotechnology, East China University of Science and Technology , Shanghai 200237, People's Republic of China.
J Agric Food Chem. 2017 Dec 6;65(48):10520-10525. doi: 10.1021/acs.jafc.7b03766. Epub 2017 Nov 28.
Modification of the sterol catabolism pathway in mycobacteria may result in the accumulation of some valuable steroid pharmaceutical intermediates, such as 9α-hydroxy-4-androstene-3,17-dione (9-OHAD). In previous work, sigma factor D (SigD) was identified as a negative factor of the 9-OHAD production in Mycobacterium neoaurum. Here, the deficiency of rip1 putatively coding for a regulated intramembrane proteolysis metalloprotease (Rip1), which could cleave the negative regulator of SigD (anti-SigD), enhanced the transcription of some key genes (choM1, kshA, and hsd4A) in the sterol catabolic pathway. Furthermore, the deletion of rip1 increased the consumption of phytosterols by 37.8% after 96 h of growth in M. neoaurum. The production of 9-OHAD in the engineered M. neoaurumΔkstD1ΔkstD2ΔkstD3Δrip1 (MnΔk123Δrip1) strain was ultimately increased by 27.3% compared to that in its parental strain M. neoaurumΔkstD1ΔkstD2ΔkstD3 (MnΔk123). This study further confirms the important role of SigD-related factors in the catabolism of sterols.
分枝杆菌中甾醇分解代谢途径的修饰可能导致一些有价值的甾体药物中间体的积累,例如9α-羟基-4-雄烯-3,17-二酮(9-OHAD)。在先前的工作中,σ因子D(SigD)被鉴定为新金色分枝杆菌中9-OHAD产生的负调控因子。在这里,假定编码一种受调控的膜内蛋白水解金属蛋白酶(Rip1)的rip1基因的缺失,该蛋白酶可以切割SigD的负调控因子(抗SigD),增强了甾醇分解代谢途径中一些关键基因(choM1、kshA和hsd4A)的转录。此外,在新金色分枝杆菌中生长96小时后,rip1基因的缺失使植物甾醇的消耗量增加了37.8%。与亲本菌株新金色分枝杆菌ΔkstD1ΔkstD2ΔkstD3(MnΔk123)相比,工程菌株新金色分枝杆菌ΔkstD1ΔkstD2ΔkstD3Δrip1(MnΔk123Δrip1)中9-OHAD的产量最终提高了27.3%。本研究进一步证实了SigD相关因子在甾醇分解代谢中的重要作用。