Translation in micrococcal nuclease-treated cell-free extracts from Ehrlich ascites tumor cells: Stimulation by initiation factor eIF-2B

Translation of exogenous mRNAs in micrococcal nuclease-treated extracts from Ehrlich ascites tumor cells is greatly stimulated by the addition of crude initiation factors or initiation factors eIF-2B and eIF-2 containing eIF-2B. The requirement for exogenous eIF-2B in micrococcal nuclease-treated extracts does not result from either loss or enhanced phosphorylation of eIF-2 during incubation.     

Anti HER2 ScFv-GFP融合抗体靶向检测HER2的表达

为验证真核表达的携带绿色荧光的抗HER2单链抗体应用于临床诊断HER2阳性肿瘤细胞和病理组织的可靠性,构建融合基因Anti HER2 ScFv-GFP,重组入pFAST Bac HT A载体,在昆虫细胞Sf9中表达,以Ni2+-NTA亲和层析法纯化Anti HER2 ScFv-GFP融合蛋白,测定其浓度与纯度,将同浓度的纯化蛋白分别与3种乳腺癌细胞BT474、SKBR3和MCF7各混合12 h、24 h和48 h,分析其在不同时间段结合HER2阳性肿瘤细胞的稳定性。用纯化蛋白直接检测经抗原修复的乳腺癌病理组织,与免疫组织化学法检测结果对比。结果在昆虫细胞Sf9中可观察到明显绿色荧光,纯化的融合蛋白相对分子量约60 kDa,浓度为115.5μg/mL,纯度约97%,SKBR3和BT474鉴定为HER2阳性。结合12 h、24 h、48 h后其细胞表面均有明显绿色荧光,而HER2阴性MCF7被洗脱后无荧光,该抗体滴度为1:64,48 h内该荧光抗体仍具有稳定性。携带绿色荧光的融合抗体检测病理组织与IHC法的结果完全一致。表明成功表达的携带绿色荧光的抗HER2单链抗体可特异性检测HER2阳性乳腺癌细胞BT474和SKBR3,在HER2阳性肿瘤细胞和临床病理组织检测上具有应用前景。     

不结球白菜BcLRK01基因对芜菁花叶病毒及胁迫诱导的响应

通过cDNA-AFLP技术,从芜菁花叶病毒(TuMV)侵染的不结球白菜幼叶中分离到一条差异表达的基因片段,克隆获得其cDNA全长为2 124bp,编码707个氨基酸的富亮氨酸重复类受体激酶,命名为BcLRK01。利用实时定量PCR研究了该基因在TuMV侵染及高盐、冷胁迫、水杨酸(SA)、茉莉酸(JA)、乙烯(ET)等处理下的表达情况,结果显示,TuMV侵染、高盐、冷胁迫、SA、JA和ET等均能诱导BcLRK01不同程度的表达,说明该基因可能是不结球白菜病毒病的病程相关基因,同时也参与高盐和冷胁迫以及SA、JA、ET等的信号途径。     

NbALD1 mediates resistance to turnip mosaic virus by regulating the accumulation of salicylic acid and the ethylene pathway in Nicotiana benthamiana

AGD2-LIKE DEFENCE RESPONSE PROTEIN 1 (ALD1) triggers plant defence against bacterial and fungal pathogens by regulating the salicylic acid (SA) pathway and an unknown SA-independent pathway. We now show that Nicotiana benthamiana ALD1 is involved in defence against a virus and that the ethylene pathway also participates in ALD1-mediated resistance. NbALD1 was up-regulated in plants infected with turnip mosaic virus (TuMV). Silencing of NbALD1 facilitated TuMV infection, while overexpression of NbALD1 or exogenous application of pipecolic acid (Pip), the downstream product of ALD1, enhanced resistance to TuMV. The SA content was lower in NbALD1-silenced plants and higher where NbALD1 was overexpressed or following Pip treatments. SA mediated resistance to TuMV and was required for NbALD1-mediated resistance. However, on NahG plants (in which SA cannot accumulate), Pip treatment still alleviated susceptibility to TuMV, further demonstrating the presence of an SA-independent resistance pathway. The ethylene precursor, 1-aminocyclopropanecarboxylic acid (ACC), accumulated in NbALD1-silenced plants but was reduced in plants overexpressing NbALD1 or treated with Pip. Silencing of ACS1, a key gene in the ethylene pathway, alleviated the susceptibility of NbALD1-silenced plants to TuMV, while exogenous application of ACC compromised the resistance of Pip-treated or NbALD1 transgenic plants. The results indicate that NbALD1 mediates resistance to TuMV by positively regulating the resistant SA pathway and negatively regulating the susceptible ethylene pathway.     

Low parasitism by Diaeretiella rapae (Hym.: Braconidae) of Lipaphis pseudobrassicae (Hemip.: Aphididae): pre- or post-ovipositional host resistance?

While the aphid Lipaphis pseudobrassicae (Davis) (Hemip.: Aphididae: Macrosiphini) is considered one of the preferred hosts of Diaeretiella rapae (McIntosh) (Hym.: Braconidae: Aphidiinae) in several parts of the world, field surveys in Uberlandia (Brazil) found parasitism of this aphid to not exceed 10%. This study sought to determine the cause of this low parasitism, as well as the effects of parasitism on the intrinsic growth rate of the aphid population. We evaluated parasitism, percentage emergence, developmental time, longevity, number of attacks and number of parasitoid larvae in L. pseudobrassicae and compared these to the same characteristics in Brevicoryne brassicae (L.) and Myzus persicae (Sulzer). The lowest percentage of parasitism was found in L. pseudobrassicae, followed by M. persicae and B. brassicae. The ratio between the number of parasitoid larvae and the number of ovipositions in L. pseudobrassicae ranged from 0.02 to 0.03, while, in B. brassicae, it was between 0.41 and 0.44 and, in M. persicae, between 0.62 and 0.80, indicating high mortality rates of early stages of D. rapae in L. pseudobrassicae. Parasitism by D. rapae reduced the r_m of L. pseudobrassicae. The r_m for parasitised aphids was only 63% of that for unparasitised aphids. However, no hosts died before reaching adulthood, and 83% of parasitised aphids were still able to reproduce. As a result, the r_m of the aphid was positive, resulting in population growth of L. pseudobrassicae, even among individuals parasitised during the second instar. Our results indicate the existence of L. pseudobrassicae genotypes that are completely resistant to D. rapae.     

温州湾灵昆岛东滩潮间带大型底栖动物群落的季节动态

潮间带是滩涂湿地生态系统的重要类型,由于处于海陆过渡地带,海陆环境因子的交替作用,物质交换过程复杂多变,因此潮间带底栖动物生态学的研究一直备受关注。国外的研究开展较为深入,如大型底栖动物在空白栖息地上定植过程及机制的研究,指出幼体成活率对定植存在决定性影响,探讨物种运动对滩涂大型底栖动物分布、多样性、密度和生物量在小尺度上的影响机制,     

Effects of short chain fatty acids on seedlings

Abstract. Primary roots of lettuce show no appreciable diminution of sensitivity of SCFA between 24 and 72 h, so it is likely that all actively growing primary roots are susceptible to inhibition by SCFA. While roots do not recover from long exposures to high concentrations of SCFA, partial recovery is seen following exposure to intermediate levels.
SCFA inhibit elongation of lettuce and turnip hypocotyls as well as roots. However, higher concentrations are required to produce a given inhibition of hypocotyl. In contrast with the inhibition of roots, inhibition of shoots is markedly dependent on the chain length of the fatty acid. Thus, either access to sites of action or action at the sites differs between shoots and roots of the same seedling plants.     

Non-identity of cystine lyase with β-cystathionase in turnip roots

An active preparation of cystine lyase (EC 4.4.1.-) was prepared from turnip roots and its substrate specificity examined. Only L-cysteine, cysteine-S-SO₃, and the sulphoxides of L-djenkolic acid, S-methyl-and S-ethyl-L-cysteine were substrates. L-Cystathione, L-djenkolic acid, S-methyl-and S-ethyl-cysteines were not cleaved by this enzyme. The K_m for L-cystine was 1.3 mM and L-cystathionine acted as an effective competitive inhibitor with a K_i of 0.7 mM. After dialysis against 10 mM potassium phosphate buffer pH 7.5, added pyridoxal phosphate was absolutely necessary for activity. In addition a marked stimulation was observed in the presence of ammonium sulphate. The products of the reaction were cysteine persulphide, pyruvate and presumably ammonia. The persulphide was easily demonstrated by cleavage with CN^? to yield SCN^? under conditions in which elemental sulphur was unreactive.     

苦豆子生物碱对萝卜蚜的毒力及其对几种酯酶的影响

苦豆子Sophora alopecuroids(L.)的次生代谢物质为喹诺里西定生物碱类。本研究明确了该生物碱中的野靛碱对萝卜蚜(Lipaphis erysimi)有很高的毒杀作用,对其无翅成蚜的致死中浓度(LC₅₀浸渍法)为(432.59±2.12)mg/L,优于著名的杀蚜生物碱毒黎碱和烟碱,两者对该试虫的LC₅₀分别为(684.70±2.28)mg/L和(1090.65±2.01)mg/L。用小菜蛾(Plutella xylostella)幼虫作试虫,得知苦豆子7种主要生物碱对昆虫的乙酰胆碱酯酶(AChE)有抑制作用,其抑制程度排序为：总碱>野靛碱>槐胺碱>槐定碱>槐果碱>氧化苦参碱>苦参碱>苦豆碱。野靛碱和苦豆碱对a-乙酸萘酯酶、a-乙酸萘酯羧酸酯酶及酯酶同功酶的活性亦表现不同程度的抑制作用。