Molecular cloning of the cDNA encoding laccase from Trametes versicolor and heterologous expression in Pichia methanolica

A cDNA encoding for laccase was isolated from the ligninolytic fungus Trametes versicolor by RNA-PCR. The cDNA corresponds to the gene Lcc1, which encodes a laccase isoenzyme of 498 amino acid residues preceded by a 22-residue signal peptide. The Lcc1 cDNA was cloned into the vectors pMETA and pMETαA and expressed in Pichia methanolica. The laccase activity obtained with the Saccharomyces cerevisiae α-factor signal peptide was found to be twofold higher than that obtained with the native secretion signal peptide. The extracellular laccase activity in recombinants with the α-factor signal peptide was 9.79 U ml⁻¹. The presence of 0.2 mM copper was necessary for optimal activity of laccase. The expression level was favoured by lower cultivation temperature. The identity of the recombinant protein was further confirmed by immunodetection using Western blot analysis. As expected, the molecular mass of the mature laccase was 64.0 kDa, similar to that of the native form.     

里氏木霉306生物合成t-PA的代谢调节机制的研究

对基因工程菌株里氏木霉 (Trichodermareesei) 30 6生物合成组织型纤溶酶原激活剂 (t PA)的代谢调节机制进行了研究。在基础发酵条件下 ,L 山梨糖、D 果糖、可溶性纤维素、CMC、麦芽糖、乳糖和棉子糖等单糖及多糖对t PA生物合成都有诱导作用 ,其中L 山梨糖的诱导效果最好 ,加量以 1 .0 %为宜。葡萄糖及其中间代谢产物对t PA的生物合成产生分解代谢物阻遏作用。纤维二糖在低浓度时可以促进t PA的生物合成而在高浓度时对t PA生物合成起反馈阻遏作用     

团头鲂寄生吸管虫一新种,双泡毛管虫的研究

描述了寄生在团头鲂(Megalobrama amblycephala)鳃上的一吸管虫新种,双泡毛管虫。活体无色透明至淡黄色,正面观为卵圆形至长椭圆形,稍扁平;侧面观为棒状或香肠状,常附着在鳃小片上。身体的表膜中有不明显的细小颗粒。吸管指状,一束,着生在虫体前端,一般有4—8根,最多达23根,收缩时其表面出现明显的螺旋纹8—11个。两个伸缩泡,交替地进行伸缩,彼此间隔约为10μm,位于吸管基部的胞质中。大核短杆状或椭圆形,核膜明显,染色质均匀。小核圆球形。成虫和幼虫没有固着柄,游泳幼虫的纤毛带宽6.0—7.0μm,由7—11行纤毛纹组成,无锥形的钻孔器。       

GPER1 Modulates Synaptic Plasticity During the Development of Temporal Lobe Epilepsy in Rats

G-protein coupled estrogen receptor 1 (GPER1) is a novel type of estrogen receptor. Several studies have shown that it has an anti-inflammatory action,which plays an important role in remyelination and cognitive ability adjustment. However, whether it is involved in the development of temporal lobe epilepsy (TLE) is still unknown. The present study established a TLE model by intraperitoneal injection of lithium chloride (3 mmol/kg) and pilocarpine (50 mg/kg) in rats to study the effect of GPER1 in the synaptic plasticity during the development of temporal lobe epilepsy. A microinjection cannula was implanted into the lateral ventricle region of rats via a stereotaxic instrument. G-1 is the specific GPER1 agonist and G15 is the specific GPER1 antagonist. The G1 or G15 and Dimethyl sulfoxide were injected into the rat brains in the intervention groups and control group, respectively. After G1 intervention, the learning and memory abilities and hippocampal neuron damage in epileptic rats were significantly improved, while G15 weakened the neuroprotective effect of GPER1. Meanwhile, G1 controlled the abnormal formation of hippocampal mossy fiber sprouting caused by seizures, and participated in the regulation of synaptic plasticity by reducing the expression of Synapsin I and increasing the expression of gephyrin. Inhibitory synapse gephyrin may play a significant role in synaptic plasticity.

     

显著六鞭毛虫超微结构的观察

作者对显著六鞭毛虫作了超微结构的观察。两个胞核平行,靠近或稍旋转。两根Ｒ鞭毛的外侧具有发达的粗内质网。近内质网处的胞质向体外突出成两个小突起。胞质内具线粒体,高尔基体等胞器。     

利用细胞质导入法选育嗜杀啤酒酵母

利用细胞质导入(Cytoduction)法中的核融合缺陷细胞融合技术,在对酿酒酵母(Saccharomyces cerevisiae)D518菌株不做任何遗传标记,将嗜杀酵母5045菌株的嗜杀质粒转移到受体菌D518中,获得了具有两亲株优良性状的融合子KD102菌株。对融合子分析表明:融合子遗传性状稳定,不仅含有供体菌5045的嗜杀质粒,而且受体菌D518的核基因被原封不动地保留下来,为异质体细胞(Heteroplasmon)。将融合子KD102菌株用于小型、中型及生产性酿酒试验,结果表明,具有与亲株D518同样的酿造特性。在发酵过程中,能抑制野生酵母污染,净化发酵体系。对于保证啤酒纯种酿造及提高成品酒的生物稳定性具有明显效果。     

Expression and Secretion of an Acid-Stable <Emphasis Type="Italic">α</Emphasis>-Amylase Gene in Bacillus Subtilis by <Emphasis Type="Italic">SacB</Emphasis> Promoter and Signal Peptide

Alpha amylase gene from Bacillus licheniformis was mutated by site-directed mutagenesis to improve its acid stability. The mutant gene was expression in Bacillus subtilis under the control of the promoter of sacB gene which was followed by either the α-amylase leader peptide of Bacillus licheniformis or the signal peptide sequence of sacB gene of Bacillus subtilis. Both peptides efficiently directed the secretion of α-amylase from the recombinant B. subtilis cells. The extracellular α-amylase activities in two recombinants were 1001 and 2012 U ml⁻¹, respectively. The purity of the recombinant product was confirmed by SDS-PAGE.     

3-甾酮-1-脱氢酶基因在大肠杆菌中的表达及甾体转化研究

将简单节杆菌3-甾酮-1-脱氢酶基因(ksdD)克隆到大肠杆菌表达载体pET-22b( )上,构建重组质粒pET-ksdD,利用IPTG诱导酶在大肠杆菌BL21(DE3)中的表达,4h后取样,分别对超声破碎后的上清和沉淀进行SDSPAGE和酶活分析,结果表明表达出的3-甾酮-1-脱氢酶的分子量大约为56kD,超声破碎后的细胞破碎液对4-AD的转化率较简单节杆菌提高了近10倍.     

山西运城盐湖土壤沉积物细菌多样性及影响因素分析

地处山西省西南部的运城盐湖历史悠久,气候特征与地理环境独特,蕴藏着丰富的微生物资源,研究其土壤沉积物生态系统对了解盐碱地土壤细菌多样性及其功能具有重要意义。【目的】探究运城盐湖土壤与沉积物中细菌的多样性,分析其影响因素,为盐碱地土壤生态系统的可持续管理和纯培养物挖掘提供科学依据与参考。【方法】对运城盐湖6个采样点的18个样品进行土壤理化分析,结合16S rRNA基因的扩增子高通量测序,分析环境因素对细菌多样性的影响。【结果】假单胞菌门(Pseudomonadota)、拟杆菌门(Bacteroidota)和芽孢杆菌门(Bacillota)为运城盐湖土壤微生物的优势类群,多样性和群落组成分析显示不同采样点间的微生物存在明显差异。典型相关分析(canonical correlation analysis, CCA)表明,总溶解固体(total dissolved solids, TDS)、总氮(total nitrogen, TN)、总碳(total carbon, TC)和SO₄^2-对土壤微生物多样性的影响最大,其次为Na⁺、Ca²⁺、Cl^-、土壤有效磷(available phosphorous, A-P)和pH,HCO₃^-、硝态氮(nitrate nitrogen, NO₃^--N)、氨态氮(ammonia nitrogen, NH₄⁺-N)、K⁺和Mg²⁺的影响较小。【结论】运城盐湖土壤微生物拥有较高的多样性,与环境因子关系密切。本研究完善了运城盐湖土壤细菌资源的生物信息,为盐湖细菌资源的挖掘和研究提供了理论依据。