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首页> 外文期刊>Microbial Cell Factories >Subtilisin QK-2: secretory expression in Lactococcus lactis and surface display onto gram-positive enhancer matrix (GEM) particles
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Subtilisin QK-2: secretory expression in Lactococcus lactis and surface display onto gram-positive enhancer matrix (GEM) particles

机译:枯草杆菌蛋白酶QK-2:在乳酸乳球菌中的分泌表达和在革兰氏阳性增强剂基质(GEM)颗粒上的表面展示

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Background Purified from the supernatant of Bacillus subtilis QK02 culture broth, Subtilisin QK-2 is a type of effective thrombolytic reagent that has great exploitable potential. However, the unbearable flavor that occurs with fermentation and the complicated methods that are required to obtain pure products limit the application of this enzyme. Lactic acid bacteria (LAB)-based delivery vehicles are promising as cheap and safe options for medicinal compounds. The secretory expression and surface display using LAB may popularize Subtilisin QK-2 more easily and conveniently with minimal adverse effects. Results Subtilisin QK-2 was expressed successfully in two forms using lactic acid bacteria. For the secretory expression in Lactococcus lactis, Subtilisin QK-2 was efficiently secreted into the culture using the promoter P nisA and signal peptide SPUsp. The expression levels were not different in L. lactis NZ9000 and NZ3900 without the effect of different selection markers. However, leaky expression was only detected in L. lactis NZ3900. The biological activity of this secreted Subtilisin QK-2 was enhanced by modulating the pH of medium to slightly alkaline during induction and by codon optimization of either the entire gene sequence ( qk′ ) or only the propeptide gene sequence ( qkpro′ ). For surface display onto gram-positive enhancer matrix (GEM) particles, n LysM repeats from the C-terminal region of the major autolysin AcmA of L. lactis were fused to either the C-terminus (n?=?1, 3, 5) or the N-terminus (n?=?1) of the Subtilisin QK-2. These fusion proteins were secreted into the culture medium, and the QK-3LysM was able to bind to the surface of various LAB GEM particles without a loss of fibrinolytic activity. Furthermore, the binding capacity significantly increased with a higher concentration of QK-3LysM. Compared to the free-form Subtilisin QK-2, the QK-3LysM displayed on the surface of GEM particles was more stable in the simulated gastric juice. Conclusions Combined with the safety and popularity of LAB, Subtilisin QK-2 may be easily applied worldwide to prevent and control thrombosis diseases.
机译:背景技术从枯草芽孢杆菌QK02培养液的上清液中纯化的枯草杆菌蛋白酶QK-2是一种有效的溶栓剂,具有很大的开发潜力。然而,发酵产生的难以忍受的味道以及获得纯产物所需的复杂方法限制了该酶的应用。基于乳酸菌(LAB)的递送载体有望作为药用化合物的廉价和安全选择。使用LAB的分泌表达和表面展示可以更轻松,更方便地将枯草杆菌蛋白酶QK-2普及,且副作用最小。结果枯草杆菌蛋白酶QK-2成功地用乳酸菌以两种形式表达。为了在乳酸乳球菌中分泌表达,枯草杆菌蛋白酶QK-2通过启动子P nisA 和信号肽SP Usp 有效地分泌到培养物中。乳酸乳球菌NZ9000和NZ3900的表达水平没有不同选择标记的影响。然而,仅在乳酸乳球菌NZ3900中检测到渗漏表达。通过在诱导过程中将培养基的pH值调节为弱碱性,以及通过对整个基因序列(qk')或仅对前肽基因序列(qkpro')进行密码子优化,可以增强这种分泌的枯草杆菌蛋白酶QK-2的生物活性。为了在革兰氏阳性增强剂基质(GEM)颗粒上进行表面展示,将乳酸乳球菌主要自溶素AcmA的C端区域的n个LysM重复序列融合到任一C端(n≥1、3、5)。 )或枯草杆菌蛋白酶QK-2的N端(n?=?1)。这些融合蛋白被分泌到培养基中,并且QK-3LysM能够与各种LAB GEM颗粒的表面结合,而不会降低纤溶活性。此外,随着QK-3LysM浓度的增加,结合能力显着提高。与游离形式的枯草杆菌蛋白酶QK-2相比,GEM颗粒表面显示的QK-3LysM在模拟胃液中更稳定。结论枯草杆菌蛋白酶QK-2结合LAB的安全性和受欢迎程度,可能在世界范围内容易地用于预防和控制血栓形成疾病。

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