Suppr超能文献

敲除甘油代谢途径能够利用甘油作为共溶剂高效地进行分枝菌属植物甾醇转化。

Knockout of glycerol metabolic pathways enables efficient mycolicibacterial phytosterol conversion using glycerol as cosovlent.

作者信息

Song Shikui, Wang Ye, Yu Jinpeng, Ma Qianqian, Cheng Xiyao, Zhang Baoguo, Su Zhengding

机构信息

Xinjiang Key Laboratory of Special Species Conservation and Regulatory Biology, College of Life Sciences, Xinjiang Normal University, Urumqi, 830054, Xinjiang, China.

Institute of Materia Medica, School of Pharmaceutical Sciences, Xinjiang University, Urumqi, 830017, Xinjiang, China.

出版信息

Appl Microbiol Biotechnol. 2025 Jul 21;109(1):169. doi: 10.1007/s00253-024-13360-7.

Abstract

Mycobacterial phytosterol conversion naturally occurs within a vegetable oil environment, a process that has been widely adopted in water‒oil two-phase fermentation to produce active pharmaceutical intermediates of steroids. The use of hydroxypropyl-β-CD (HP-β-CD) as a potential replacement for vegetable oils has been explored. However, both approaches encounter challenges, particularly the need for a high concentration of either vegetable oil or HP-β-CD in the fermentation medium, which significantly affects the efficiency of mycobacterial phytosterol conversion as well as the recovery of the resulting products. In this study, we demonstrated that the knockout of glycerol metabolic pathways enables the utilization of glycerol as cosovlent for efficient phytosterol conversion in Mycolicibacterium neoaurum HGMS6, an industrial strain known for its production of 4-androstene-3,17-dione (4-AD). Our bioinformatic analysis revealed two parallel glycerol metabolic pathways in the HGMS6 strain. These pathways are independently initiated by glycerol kinase (GLPK) and glycerol dehydrogenase (ADHC). To investigate their roles, we conducted gene knockout experiments in which both the glycerol kinase gene (glpk) and the glycerol dehydrogenase gene (adhc) were targeted in HGMS6, resulting in the creation of a glycerol metabolism-deficient mutant, denoted HGMS6. This double mutant exhibited complete inactivation of mycobacterial glycerol metabolism without any adverse effects on mycobacterial growth when cultured in conventional fermentation medium containing glucose. We then evaluated HGMS6 in an aqueous phase fermentation medium and determined that fermentation media consisting of 10% glycerol and 0.5% HP-β-CD provided the optimal conversion efficiency. In pilot-scale fermentation experiments, this mutant was highly efficient at converting phytosterols, achieving a remarkable conversion rate of up to 83.8% (mol/mol%). This bioconversion level was on par with that of HGMS6 and HGMS6 when operating in vegetable oil- or HP-β-CD-containing fermentation media. This study provides a promising strategy for enhancing the efficiency of mycobacterial phytosterol conversion. KEY POINTS: • TheGLPK and ADHC of M. neoaurum were confirmed and examined. • The enzymology of ADHC and GLPK was characterized in vitro. • An adhc/glpk-knockout mutant efficiently converts phytosterols in fermentation media containing 10% (w/v) glycerol and 0.5%(w/v) HP-β-CD.

摘要

分枝杆菌的植物甾醇转化自然发生在植物油环境中,这一过程已在水 - 油两相发酵中广泛应用于生产甾体类活性药物中间体。人们已探索使用羟丙基 -β-环糊精(HP-β-CD)作为植物油的潜在替代品。然而,这两种方法都面临挑战,特别是在发酵培养基中需要高浓度的植物油或HP-β-CD,这显著影响了分枝杆菌植物甾醇转化的效率以及所得产物的回收。在本研究中,我们证明敲除甘油代谢途径能够使甘油作为共溶剂,在新金色分枝杆菌HGMS6(一种以生产4-雄烯-3,17-二酮(4-AD)而闻名的工业菌株)中实现高效的植物甾醇转化。我们的生物信息学分析揭示了HGMS6菌株中两条平行的甘油代谢途径。这些途径分别由甘油激酶(GLPK)和甘油脱氢酶(ADHC)独立启动。为了研究它们的作用,我们进行了基因敲除实验,在HGMS6中靶向甘油激酶基因(glpk)和甘油脱氢酶基因(adhc),从而创建了一个甘油代谢缺陷型突变体,命名为HGMS6。当在含有葡萄糖的常规发酵培养基中培养时,这个双突变体表现出分枝杆菌甘油代谢的完全失活,且对分枝杆菌生长没有任何不利影响。然后我们在水相发酵培养基中评估了HGMS6,并确定由10%甘油和0.5%HP-β-CD组成的发酵培养基提供了最佳转化效率。在中试规模发酵实验中,该突变体在植物甾醇转化方面非常高效,转化率高达83.8%(摩尔/摩尔%)。这一生物转化水平与在含植物油或HP-β-CD的发酵培养基中操作的HGMS6和HGMS6相当。本研究为提高分枝杆菌植物甾醇转化效率提供了一种有前景的策略。要点:• 确认并研究了新金色分枝杆菌的GLPK和ADHC。• 在体外对ADHC和GLPK的酶学性质进行了表征。• 一个adhc/glpk敲除突变体在含有10%(w/v)甘油和0.5%(w/v)HP-β-CD的发酵培养基中能高效转化植物甾醇。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验