Reaction intensification for biocatalytic production of polyphenolic natural product di-C-β-glucosides

Polyphenolic aglycones featuring two sugars individually attached via C-glycosidic linkage (di-C-glycosides) represent a rare class of plant natural products with unique physicochemical properties and biological activities. Natural scarcity of such di-C-glycosides limits their use-inspired exploration as pharmaceutical ingredients. Here, we show a biocatalytic process technology for reaction-intensified production of the di-C-β-glucosides of two representative phenol substrates, phloretin (a natural flavonoid) and phenyl-trihydroxyacetophenone (a phenolic synthon for synthesis), from sucrose. The synthesis proceeds via an iterative two-fold C-glycosylation of the respective aglycone, supplied as inclusion complex with 2-hydroxypropyl β-cyclodextrin for enhanced water solubility of up to 50 mmol/L, catalyzed by a kumquat di-C-glycosyltransferase (di-CGT), and it uses UDP-Glc provided in situ from sucrose by a soybean sucrose synthase, with catalytic amounts (≤3 mol%) of UDP added. Time course analysis reveals the second C-glycosylation as rate-limiting (0.4–0.5 mmol/L/min) for the di-C-glucoside production. With internal supply from sucrose keeping the UDP-Glc at a constant steady-state concentration (≥50% of the UDP added) during the reaction, the di-C-glycosylation is driven to completion (≥95% yield). Contrary to the mono-C-glucoside intermediate which is stable, the di-C-glucoside requires the addition of reducing agent (10 mmol/L 2-mercaptoethanol) to prevent its decomposition during the synthesis. Both di-C-glucosides are isolated from the reaction mixtures in excellent purity (≥95%), and their expected structures are confirmed by NMR. Collectively, this study demonstrates efficient glycosyltransferase cascade reaction for flexible use in natural product di-C-β-glucoside synthesis from expedient substrates.     

绒山羊源大肠杆菌噬菌体φPTK的分子生物学特性及对小鼠大肠杆菌感染的防治效果

【背景】抗生素耐药问题是影响人类及养殖业健康的重要因素,噬菌体能特异性裂解细菌,成为抗生素替代品研究热点,是解决抗生素耐药难题、促进养殖业健康发展的新途径。【目的】通过研究绒山羊源大肠杆菌烈性噬菌体φPTK (phage target of K1)的分子生物学特性,同时利用小鼠感染模型研究φPTK对小鼠大肠杆菌感染的防治效果,为绒山羊大肠杆菌病的防控提供新策略。【方法】用聚乙二醇-氯化钠(PEG 8000-NaCl)浓缩φPTK后,采用透射电子显微镜观察其超微形态结构;运用苯酚-氯仿法提取φPTK核酸后通过Illumina HiSeq高通量测序分析其全基因组结构,使用Mauve比较基因组学分析,通过MEGA绘制噬菌体进化树;通过构建小鼠感染模型分析φPTK对小鼠感染大肠杆菌的防治效果。【结果】透射电镜显示φPTK头部为正多面体形,直径90 nm,有长约112 nm、直径约18 nm的可收缩长尾;φPTK基因组全长169 688 bp,GC含量37.72%,有264个开放阅读框,含穿孔素-裂解酶(holin-lysin)裂解系统,有抗穿孔素蛋白和裂解抑制辅助蛋白,未发现抗生素耐药基因和毒力基因;比较基因组分析表明,φPTK为一株新的绒山羊源大肠杆菌烈性噬菌体;小鼠大肠杆菌感染前和感染后分别使用φPTK进行预防和治疗的试验表明,未使用φPTK的阳性对照组小鼠全部死亡,预防组和治疗组小鼠存活率分别为80%和60%。【结论】噬菌体φPTK是一株能够在小鼠大肠杆菌感染中具有较好预防效果的有尾噬菌体目(Caudovirales)肌尾噬菌体科(Myoviridae)绒山羊源大肠杆菌烈性噬菌体,本研究为绒山羊噬菌体生物制剂的创制奠定了基础。     

气候变化和经济发展对肾综合征出血热发生的影响

肾综合征出血热(hemorrhagic fever with renal syndrome, HFRS)是一种啮齿动物传播的自然疫源性疾病, 危害严重, 已成为全球重要的公共卫生问题。本研究采用数理统计模型及小波分析方法, 对陕西省西安市鄠邑区1984-2016年HFRS的发生与鼠类、气候和经济因素的关系进行分析, 探讨气候和经济因素对HFRS发生的影响。小波分析结果表明, 该地区的HFRS暴发史可能分为两个时期, 推测每个时期具有不同的主要宿主, 在2002年褐家鼠(Rattus norvegicus)可能取代黑线姬鼠(Apodemus agrarius)成为HFRS疫源地的主要宿主。广义可加模型模拟结果表明, HFRS的发生与1984-2001年黑线姬鼠密度间存在极显著非线性效应(F_2.06,9.02 = 102.415, P < 0.01), 两者间显现为正相关; 与2002-2016年的褐家鼠密度间呈正相关(F_1.67,9.02 = 73.929, P < 0.01); HFRS主要宿主的这种变化可能与当地气候变化和经济发展有关: HFRS的发生与年平均温度存在极显著的非线性效应(F_2.93,9.02 = 12.164, P < 0.01), 两者间呈负相关; 同样, HFRS的发生与上一年的国内生产总值(GDP)也存在显著非线性效应(F_1.70,9.02 = 2.917, P < 0.05), 两者间也呈负相关。结构方程模型通过直接和间接的影响途径证明了这种转移机制, 发现温度对HFRS发生有显著的直接负向影响以及通过褐家鼠的间接正向影响; GDP对HFRS发生有直接的负向影响。本研究表明HFRS的发生与气候变化和经济发展相关, 两者均能影响HFRS的暴发, 该结论有助于今后更好地对HFRS疾病进行预防和控制。     

气候因素对黑线姬鼠种群动态影响的非线性效应

受全球气候变化的影响,气候因素与害鼠种群变化之间的关系成为害鼠防治研究中的热点问题。以西安市长安区周边分布的黑线姬鼠为研究对象,通过标志重捕法进行种群动态监测,掌握其种群数量的动态变化规律,并结合非线性的统计方法广义可加模型,对该地区2015—2018年黑线姬鼠种群密度和气候因素数据进行分析,探讨该鼠种群变化与气候因素之间的关系。结果表明,该地区黑线姬鼠种群数量总体显现为下降趋势。黑线姬鼠种群密度存在显著的正向自我调节效应(F_(1.00, 5.77)=27.062,P0.01),且与上一月种群密度存在线性的正相关。当月平均温度与该鼠种群密度之间存在显著的非线性效应(F_(1.90, 5.77 )=4.696,P0.05),两者之间显现为钟型关系,当温度21℃时,两者之间显现为正相关,黑线姬鼠种群密度随温度的升高而升高,反之显现为负相关。当月累计降雨量与其种群密度之间也存在显著的非线性效应(F_(1.87, 5.77)=3.879,P0.05),同样,两者之间也显现为钟型关系,当降雨量90 mm时,两者之间显现为负相关,种群密度随降雨量的增加而降低,反之显现为正相关。因此,温度和降雨对黑线姬鼠种群变化具有调节作用,低温干旱和高温多雨均不适合该鼠的繁殖与生长。     

不同地点51个长白落叶松无性系苗期生长变异和遗传稳定性分析

长白落叶松是我国东北林区非常重要的速生用材树种之一。以不同地点51个长白落叶松无性系为材料,对其2年生苗高和地径进行调查分析,探讨其苗期生长变异和遗传稳定性。结果表明:长白落叶松无性系苗高和地径在地点间、无性系间、地点×无性系间差异均达到极显著水平(P<0.01);不同地点苗高和地径的表型变异系数处于23.89%~36.82%,除四平试验点的地径重复力为0.172外,不同地点苗高和地径的重复力均处于0.573~0.891;遗传稳定性分析结果表明,无性系LO 13等28个无性系的遗传稳定性较高;相关分析结果表明苗高与地径呈极显著正相关关系;利用多性状综合评价法,以20%的入选率对无性系进行选择,不同地点均选出10个综合表现较好的无性系,其中无性系LO 10和LO 26在不同地点均被入选优良无性系,且其遗传稳定性较强,可将其初选为优良无性系。     

MicroRNA-217 Promotes Angiogenesis of Human Cytomegalovirus-Infected Endothelial Cells through Downregulation of SIRT1 and FOXO3A

Human cytomegalovirus(HCMV) infection has been shown to contribute to vascular disease through the induction of angiogenesis. However, the role of microRNA in angiogenesis induced by HCMV infection remains unclear. The present study was thus designed to explore the potential effect of miR-1217 on angiogenesis and to disclose the underlying mechanism in endothelial cells. We found that HCMV infection of endothelial cells(ECs) enhanced expression of miR-217 and reduced SIRT1 and FOXO3A protein level in 24 hours post infection(hpi). Transfection of miR-217 inhibitor not only depressed cellular migration and tube formation induced by HCMV infection, but also enhanced SIRT1 and FOXO3A protein expression. Additionally, luciferase assay confirmed that miR-217 directly targeted FOXO3A mRNA 3`UTR. Furthermore, pretreatment with resveratrol depressed motility and tube formation of HCMV-infected ECs, which could be reversed by SIRT1 siRNA. Similarly, delivery of FOXO3A overexpression lentivirus suppressed proliferative rate, migration and tube formation of HCMV-infected ECs, which reversed by transfection of FOXO3A siRNA. In summary, HCMV infection of endothelial cells induces angiogenesis by both of miR-217/SIRT1 and miR-217/FOXO3A axis.