抗草甘膦酵母菌ZM-1的分离鉴定及其生长降解特性

以福州市郊区的耕作土壤为研究材料, 利用草甘膦为选择压力, 通过富集、驯化培养, 分离出一株对草甘膦具有高耐受和降解作用的酵母菌菌株ZM-1, 结合生理生化特征及26S rDNA D1/D2区序列分析将其初步鉴定为胶红酵母菌(Rhodotorula mucilaginosa)。菌株ZM-1能以草甘膦为唯一碳、氮源生长, 对草甘膦的最高耐受浓度为50 g/L。在草甘膦初始浓度为1 g/L的无机盐培养基中, 30°C、150 r/min 摇床振荡培养7 d, 草甘膦降解率为85.38%。适合菌株ZM-1生长及降解草甘膦的最佳条件为: 草甘膦初始浓度1 g/L, 接种量4%, 温度30°C, pH 值5.5-6.0, 装料量50 mL/250 mL。菌株ZM-1是一株良好的草甘膦耐受菌, 可用于草甘膦污染环境的生物修复, 也可能成为转基因抗草甘膦作物的一个很好资源。     

多噬伯克霍尔德氏菌WS-FJ9对草甘膦的降解特性

长期或不当施用草甘膦会对非靶标生物和环境造成破坏作用。微生物是生物修复的重要生物资源,利用微生物及其产生的降解酶处理环境中有机磷农药的方法,已显示出良好的应用前景,是近年来研究有机磷农药降解的主要发展方向。本文目的在于研究分离于松树根际土壤的高效解磷细菌多噬伯克霍尔德氏菌（Burkholderia multivorans）WS-FJ9菌株对草甘膦的降解特性及其降解条件的优化。采用添加不同浓度草甘膦NA平板接种WS-FJ9菌株观察其对草甘膦的耐受性;分别以草甘膦为唯一碳源、氮源或磷源,探讨WS-FJ9菌株对草甘膦的利用状况;采用低进水量间歇式反应器法（FBR）测定了WS-FJ9菌株降解草甘膦动力学参数;利用Plackett-Burman（PB）、Central Composite Design（CCD）试验设计及响应面分析法（RSM）筛选与优化影响WS-FJ9菌株降解草甘膦的主要因素。WS-FJ9菌株有效降解草甘膦的最大耐受浓度为0.4%; WS-FJ9菌株在以草甘膦为唯一碳源、氮源或磷源培养基上均能正常生长;WS-FJ9菌株对草甘膦的亲和性常数（Ks值）为65 μL?mL-1,对草甘膦降解的极限浓度（Smin）为21.9 μL?mL-1;通过PB试验,筛选出3个影响菌株降解草甘膦的关键因素为培养温度、葡萄糖及硫酸铵的加入量,通过CCD设计及响应面法优化分析得到影响草甘膦降解率的关键因素的二阶模型,确定了WS-FJ9菌株降解草甘膦的最优实验操作条件为：培养温度27.7℃,葡萄糖和硫酸铵的加入量分别为0.67、0.50 g?L-1。实验条件下WS-FJ9菌株对草甘膦的降解率最高为72.83％。     

海洋石油降解微生物及其降解机理

微生物修复作为一种新型环保的生物修复技术,已成为海洋石油污染生物修复的核心技术。对海洋石油降解微生物的种类即细菌、蓝藻、真菌以及藻类进行了总结,对微生物对石油烃的降解途径与降解机理进行了综述。微生物降解烷烃的过程包括末端氧化、烷基氢过氧化物以及环己烷降解3种形式。微生物对芳香烃的降解是通过芳香烃被氧化酶氧化导致苯环开环来实现的。微生物对多环芳烃的降解是在单加氧酶或双加氧酶的催化作用下被最终降解为二氧化碳和水而被分解。并对影响石油烃降解微生物的因素包括温度、营养物质等因素进行了分析。     

土壤中高环多环芳烃微生物降解的研究进展

微生物修复是去除土壤中多环芳烃(PAHs)的主要措施。本文以微生物修复PAHs污染土壤的理论基础及其难点为主线,全面综述了土壤中高环PAHs的微生物降解机理。近年来,富集分离得到的以高环PAHs为唯一碳源和能源的优势降解菌逐渐增多,其中,主要是代谢降解四环PAHs的单株降解菌,一些降解菌还能以共代谢方式利用五环PAHs。高环PAHs污染土壤修复的一个难点是其低生物可利用性,微生物通过释放生物表面活性剂、形成生物膜以及分泌胞外多糖提高高环PAHs的生物可利用性,从而加速其降解。真菌和细菌联合作用能增强污染土壤实地修复的效果。因此,通过微生物修复技术来去除土壤中PAHs具有环境友好性、经济适用性以及可持续应用性。     

环境中污染物降解基因的水平转移(HGT)及其在生物修复中的作用

水平基因转移是不同于垂直基因转移的遗传物质的交流方式.在污染环境这一特异生态环境中,降解基因的水平转移有着独特的功能与作用.研究环境中污染物降解基因在微生物间的水平转移,更深入地了解微生物种群适应污染环境的机理,对于评价污染物的环境毒理、生物可降解性以及污染环境的可修复潜力具有重要参考价值.在污染物生物修复实践中,可以通过调控降解基因的水平转移,增强污染环境中微生物的降解能力,更有效地发挥生物修复作用.文章将对环境中细菌间基因交流的机制,污染物降解基因的水平转移对微生物适应污染环境的机理、水平基因转移对代谢途径的进化及其对污染物生物修复作用的影响等方面的研究进展做一综述.     

植物法生物修复PAHs和矿物油污染土壤的调控研究

选择苜蓿草为供试植物,以污染物含量水平、专性细菌和真菌及有机肥为调控因子,进行了植物法生物修复多环芳烃(PAHs)和矿物油污染土壤的调控研究。结果表明,PAHs和矿物油的降解率与有机肥含量呈正相关,增加有机肥5%,可提高矿物油降解率17.6%～25.6%,PAHs降解率9%.在植物存在条件下,土壤微生物降解功能增强。多环芳烃总量的平均降解率比无植物对照土壤提高2.0%～4.7%.投加特性降解真菌可不同程度地提高土壤PAHs总量和矿物油的降解率。真菌对萤蒽、芘和苯(a)蒽/(艹屈)的降解有明显促进作用。而细菌能明显提高苊稀/芴、蒽和苯(a)萤蒽/苯(k)萤蒽的降解率。     

取代脲类除草剂的微生物降解

取代脲类除草剂主要用来防除一年生禾本科杂草和阔叶杂草,自20世纪中期推入市场以来,在世界范围内被广泛使用,已成为重要的除草剂之一。随着取代脲类除草剂的持续施用,其在环境中的残留严重超标,危害日益凸显。因此,取代脲类除草剂在环境中的吸附、迁移和降解等行为备受关注。研究表明细菌降解N,N-二甲基取代脲类除草剂主要是通过连续脱甲基作用后断脲桥降解,而降解N-甲氧基-N-甲基取代脲类除草剂是通过脲桥的直接断裂。真菌降解取代脲类除草剂的途径则较为复杂,尚需进一步阐明。本文综述了近年来分离筛选的取代脲类除草剂降解菌株及其降解途径的最新研究进展,为取代脲类除草剂污染环境的生物修复研究提供参考。     

细菌降解萘、菲的代谢途径及相关基因的研究进展

多环芳烃(Polycyclic aromatic hydrocarbons,PAHs)是一类在环境中广泛存在的具有毒性的污染物,微生物降解是其在自然界中降解的主要途径,因而尤为重要。随着研究的深入,关于微生物降解PAHs的分子降解机制、途径等的认识逐渐积累。以下对细菌降解萘、菲的研究进展进行了概述,介绍了萘的水杨酸降解途径,菲的水杨酸、邻苯二甲酸及其他降解途径,同时也包括降解过程中涉及的降解基因簇,如nah-like、phn、phd、nid和nag等以及细菌在PAHs胁迫条件下其他相关基因的表达与调节等方面的最新进展。这些进展可为降解菌株的分子及遗传机制研究提供理论依据,将促进通过基因工程优化降解菌、更有效地检测PAHs环境污染及实现PAHs污染的生物修复。     

微生物对三苯基甲烷类染料脱色的研究进展

三苯基甲烷染料广泛应用于纺织印染、医药、生物染色、造纸、皮革、食品及化妆品等领域, 常见的有作为抗菌剂的孔雀石绿和结晶紫等。由于其特殊的化学结构, 在环境中较稳定且难以降解脱色, 因此其生物脱色降解的研究可为印染废水处理和染料污染环境的生物修复提供理论依据。本文从细菌、放线菌、真菌及藻类等微生物对三苯基甲烷类染料降解脱色研究新进展做综述。通过分析不同微生物脱色三苯基甲烷类染料的中间产物来探讨其降解机理和降解途径, 同时论及功能酶的分离纯化、酶学特性及其编码基因的克隆表达新进展, 并分别从基础理论和应用两方面对微生物降解三苯基甲烷类染料未来的研究方向进行了展望。     

瘤胃微生物对纤维素的降解及其应用

瘤胃微生物主要包括细菌、真菌和原生动物。其中,瘤胃细菌和瘤胃真菌能分泌纤维素酶,对纤维素有较强的降解能力,主要介绍了瘤胃微生物对纤维素的降解作用及其广阔的应用前景。     

Recent advances in the study of Kaposi's sarcoma-associated herpesvirus replication and pathogenesis

It has now been over twenty years since a novel herpesviral genome was identified in Kaposi's sarcoma biopsies. Since then, the cumulative research effort by molecular biologists, virologists, clinicians, and epidemiologists alike has led to the extensive characterization of this tumor virus, Kaposi's sarcoma-associated herpesvirus(KSHV; also known as human herpesvirus 8(HHV-8)), and its associated diseases. Here we review the current knowledge of KSHV biology and pathogenesis, with a particular emphasis on new and exciting advances in the field of epigenetics. We also discuss the development and practicality of various cell culture and animal model systems to study KSHV replication and pathogenesis.     

A Unique Protease Cleavage Site Predicted in the Spike Protein of the Novel Pneumonia Coronavirus (2019-nCoV) Potentially Related to Viral Transmissibility

正Dear Editor,In December 2019, a novel human coronavirus caused an epidemic of severe pneumonia(Coronavirus Disease 2019,COVID-19) in Wuhan, Hubei, China(Wu et al. 2020; Zhu et al. 2020). So far, this virus has spread to all areas of China and even to other countries. The epidemic has caused 67,102 confirmed infections with 1526 fatal cases     

Curcuminoids as inhibitors of thioredoxin reductase: A receptor based pharmacophore study with distance mapping of the active site

Curcumin is the yellow pigment of turmeric that interacts irreversibly forming an adduct with thioredoxin reductase (TrxR), an enzyme responsible for redox control of cell and defence against oxidative stress. Docking at both the active sites of TrxR was performed to compare the potency of three naturally occurring curcuminoids, namely curcumin, demethoxy curcumin and bis-demethoxy curcumin. Results show that active sites of TrxR occur at the junction of E and F chains. Volume and area of both cavities is predicted. It has been concluded by distance mapping of the most active conformations that Se atom of catalytic residue SeCYS498, is at a distance of 3.56 from C13 of demethoxy curcumin at the E chain active site, whereas C13 carbon atom forms adduct with Se atom of SeCys 498. We report that at least one methoxy group in curcuminoids is necessary for interation with catalytic residues of thioredoxin. Pharmacophore of both active sites of the TrxR receptor for curcumin and demethoxy curcumin molecules has been drawn and proposed for design and synthesis of most probable potent antiproliferative synthetic drugs.     

Comparative morphology of the carpel in the Liliaceae: Hewardieae, Petrosavieae, and Tricyrteae

The young pistils in the melanthioid tribes, Hewardieae, Petrosavieae and Tricyrteae, are uniformly tricarpellate and syncarpous. They lack raphide idioblasts. All are multiovulate, with bitegmic ovules. The Petrosavieae are marked by the presence of septal glands and incomplete syncarpy. Tepals and stamens adhere to the ovary in the Hewardieae and the Petrosavieae but not in the Tricyrteae. Two vascular bundles occur in the stamens of the Hewartlieae and Tricyrtis latifolia. Ventral bundles in the upper part of the ovary of the Hewardieae are continuous with compound septal bundles and placental bundles in the lower part. Putative ventral bundles occur in the alternate position in the Tricyrteae and putative placental bundles in the opposite. position in the Petrosavieae. The dichtomously branched stigma in each carpel of the Tricyrteae is supplied by a bifurcated dorsal bundle.     

Synthesis and antimicrobial studies of hydrazone derivatives of 4-[3-(2,4-difluorophenyl)-4-formyl-1H-pyrazol-1-yl]benzoic acid and 4-[3-(3,4-difluorophenyl)-4-formyl-1H-pyrazol-1-yl]benzoic acid

Microbial resistance to antibiotics is an unresolved global concern, which needs urgent and coordinated action. One of the guidelines of the Centers for Disease Control and Preventions (CDC) to combat antibiotic resistance is the development of new antibiotics to treat drug-resistant bacteria. In our effort to find new antibiotics, we report the synthesis and antimicrobial studies of 30 new pyrazole derivatives. These novel molecules have been synthesized by using readily available starting materials and benign reaction conditions. Some of these molecules have shown activity with MIC values as low as 0.78?µg/mL against four bacterial strains; Staphylococcus aureus, methicillin-resistant S. aureus, Bacillus subtilis, and Acinetobacter baumannii. Furthermore, active molecules are non-toxic to mammalian cell line.

     

Novel compounds with potent CDK9 inhibitory activity for the treatment of myeloma

Cyclin-dependent kinases (CDKs) and Polo-like kinases (PLKs) play key role in the regulation of the cell cycle. The aim of our study was originally the further development of our recently discovered polo-like kinase 1 (PLK1) inhibitors. A series of new 2,4-disubstituted pyrimidine derivatives were synthesized around the original hit, but their PLK1 inhibitory activity was very poor. However the novel compounds showed nanomolar CDK9 inhibitory activity and very good antiproliferative effect on multiple myeloma cell lines (RPMI-8226).