运用乙炔抑制-静态土柱培养法测定旱地土壤氮素反硝化损失

介绍了测定土壤反硝化作用的乙炔抑制 -静态土柱培养法 ,并就其应用中的一些条件进行了说明 ,内容包括土柱的取样深度、土柱取样量、土柱培养方式及基本操作程序等。最后阐述了这一方法在北京郊区土壤上的使用情况。     

杠柳根皮粗提液对菜青虫生物活性的影响

试验研究杠柳根皮粗提液对菜青虫生物活性的影响测定结果表明,杠柳根皮乙醇提取液对菜青虫的生物活性影响高于杠柳根皮氯仿提取液和石油醚提取液,杠柳根皮乙醇提取液对菜青虫幼虫有较强的拒食作用和生长抑制作用,胃毒作用一般。用100倍液杠柳根皮乙醇提取液浸叶饲喂3龄、4龄、5龄菜青虫幼虫后24h其拒食率分别为94.9%、87.8%和92.7%,拒食后幼虫的化蛹率和蛹重均比对照显著降低。100倍液杠柳根皮乙醇提取液浸叶饲喂4龄菜青虫幼虫后24h和72h其生长抑制率分别为96.6%和82.5%。杠柳根皮乙醇提取液对菜青虫成虫产卵具有明显忌避作用,用50~100倍液杠柳根皮乙醇提取液喷雾处理油菜苗后2~4d其产卵忌避率达89.5%以上。     

植物抗冻蛋白及其高级结构研究进展

抗冻蛋白是一类能控制冰晶生长和抑制冰晶之间发生重结晶的蛋白质．并具有两种明显不同的活性——热滞活性和重结晶抑制活性．植物抗冻蛋白的抗冻特性是低热滞活性和高重结晶抑制活性．植物抗冻蛋白虽然在DNA和氨基酸水平上具有较大的差异-几乎没有同源性，但却拥有相似的高级结构．冰晶结合位点也有一定的相似性．而且都可以通过“表面互补”模型较好地解释它们与冰晶之间的相互作用．全面介绍了植物抗冻蛋白的种类及特性，以及它们的高级结构和冰晶结合位点．     

4种木霉对核盘菌的抑制作用

通过对峙培养以及对木霉菌(Trichoderma spp.)次生代谢物对病原菌的抑菌率进行了测定,结果表明,供试哈茨木霉(T.harzianum)、绿色木霉(T.viride)、康氏木霉(T.koningii),以及一株未知种名的木霉菌株TY(Trichoderma sp.)均对核盘菌(Sclerotinia sclerotiorum (Lib) de Bary)有明显的抑制作用.在对峙培养中,木霉菌菌落与核盘菌的菌落相向生长一定时间后,挑取核盘菌菌落内部的菌丝进行镜检,发现有木霉菌孢子存在,且核盘菌发生菌丝变形,如原生质浓缩,菌丝断裂,或菌丝消解等现象.并发现不同种木霉所产生的次生代谢物的活性不同,对核盘菌的抑制作用也存在显著差异.     

Characterization of an Insoluble and Soluble Form of Melanin Produced by Streptomyces cavourensis SV 21, a Sea Cucumber Associated Bacterium

Melanin is a widely distributed and striking dark-colored pigment produced by countless living organisms. Although a wide range of bioactivities have been recognized, there are still major constraints in using melanin for biotechnological applications such as its fragmentary known chemical structure and its insolubility in inorganic and organic solvents. In this study, a bacterial culture of Streptomyces cavourensis SV 21 produced two distinct forms of melanin: (1) a particulate, insoluble form as well as (2) a rarely observed water-soluble form. The here presented novel, acid-free purification protocol of purified particulate melanin (PPM) and purified dissolved melanin (PDM) represents the basis for an in-depth comparison of their physicochemical and biological properties, which were compared to the traditional acid-based precipitation of melanin (AM) and to a synthetic melanin standard (SM). Our data show that the differences in solubility between PDM and PPM in aqueous solutions may be a result of different adjoining cation species, since the soluble PDM polymer is largely composed of Mg²⁺ ions and the insoluble PPM is dominated by Ca²⁺ ions. Furthermore, AM shared most properties with SM, which is likely attributed to a similar, acid-based production protocol. The here presented gentler approach of purifying melanin facilitates a new perspective of an intact form of soluble and insoluble melanin that is less chemical altered and thus closer to its original biological form.     

Semi-Synthesis,Cytotoxic Evaluation,and Structure—Activity Relationships of Brefeldin A Derivatives with Antileukemia Activity

Brefeldin A (1), a potent cytotoxic natural macrolactone, was produced by the marine fungus Penicillium sp. (HS-N-29) from the medicinal mangrove Acanthus ilicifolius. Series of its ester derivatives 2–16 were designed and semi-synthesized, and their structures were characterized by spectroscopic methods. Their cytotoxic activities were evaluated against human chronic myelogenous leukemia K562 cell line in vitro, and the preliminary structure–activity relationships revealed that the hydroxy group played an important role. Moreover, the monoester derivatives exhibited stronger cytotoxic activity than the diester derivatives. Among them, brefeldin A 7-O-2-chloro-4,5-difluorobenzoate (7) exhibited the strongest inhibitory effect on the proliferation of K562 cells with an IC₅₀ value of 0.84 µM. Further evaluations indicated that 7 induced cell cycle arrest, stimulated cell apoptosis, inhibited phosphorylation of BCR-ABL, and thereby inactivated its downstream AKT signaling pathway. The expression of downstream signaling molecules in the AKT pathway, including mTOR and p70S6K, was also attenuated after 7-treatment in a dose-dependent manner. Furthermore, molecular modeling of 7 docked into 1 binding site of an ARF1–GDP-GEF complex represented well-tolerance. Taken together, 7 had the potential to be served as an effective antileukemia agent or lead compound for further exploration.     

氟节胺抑制枇杷嫁接成苗砧木萌蘖相关机理初探

为寻找更长效、无害的化学控蘖剂以减轻田间管理劳动强度,以枇杷(Eriobotrya japonica)嫁接成苗为材料,喷施有效成分浓度为0.050%,0.071%和0.125%的氟节胺,于不同时期取样观察控蘖效果,并尝试探究相关机理。结果表明,氟节胺减少了叶片单位面积光能的吸收量、抑制了光化学转换,但叶片的热耗散量并无明显变化。进一步测定植株氧化还原状态发现,氟节胺能够快速促进细胞内超氧阴离子(O₂^.-)积累并延缓或抑制H₂O₂的转化,从而诱发氧化胁迫。由此可见,氟节胺可能通过抑制叶片光化学转换和热耗散来破坏新生萌蘖的光合性能,进而抑制其萌发生长,而成熟叶片则通过提升自身抗氧化系统活性耐受氟节胺造成的轻度胁迫。在本试验中,各浓度的氟节胺对控制砧木萌蘖有不同程度的效果,其中浓度为0.125%的氟节胺控蘖效果相对最佳,且基本不会对砧木和嫁接成苗造成持续伤害,其作为化学控蘖剂有一定的应用潜力。     

伐地那非增加EGCG-β-乳球蛋白纳米粒对肝癌细胞的抑制作用

较高浓度的EGCG才能抑制癌细胞的增殖,通过纳米化和EGCG与其他药物的联合使用是提高EGCG生物活性的重要策略。本研究将EGCG和伐地那非（VD）同时包埋于β-乳球蛋白（β-Lg）纳米载体中,制备出EGCG-VD-β-Lg纳米粒（EVβ-NPs）,体外试验证实,EVβ-NPs能提高人肝癌细胞（HepG2细胞）中Caspase-3活性,使HepG2细胞在S期产生明显的阻滞,诱发细胞核分裂,从而导致HepG2细胞凋亡。研究结果表明,将EGCG与微量的VD联合使用,并通过纳米化包埋可以显著提高EGCG的抗癌活性。这一方法在EGCG抗癌制品的开发方面具有潜在的价值。