60Co辐射诱变姬松茸突变株J3子实体不同部位的氨基酸分析研究     

黄挺俊  翁伯琦  肖淑霞  王义祥  江枝和 《食用菌学报》2005,12(4):13-16

测定并比较了60Co辐射诱变姬松茸突变株J3与原菌株J1子实体不同部位的氨基酸含量.结果表明,除菌柄和盖皮外,姬松茸突变株J3子实体其它部位的必需氨基酸、儿童氨基酸、硫氨酸、支链氨基酸、鲜味氨基酸、芳香族氨基酸和甜味氨基酸均高于原菌株J1.姬松茸突变株J3子实体中谷氨酸含量占氨基酸总量的比例分别比原菌株J1、α-酪蛋白和卵清蛋白提高34.88%、56.68%和122.32%.  相似文献   

Bcl-2 antisense oligodeoxynucleotide increases the sensitivity of HL60 and K562 cells to daunorubicin     

LEI Xiao-yong  ZHANG Huan  HE Dong-mei 《园艺学报》2003,19(2):194-197

AIM:To investigate whether the bcl-2 antisense oligonucleotide increases the sensitivity of HL60 and K562 cell lines to daunorubicin.METHODS:IC50 for HL60 and K562 was determined with MTT method, the expression levels of Bcl-2 protein were assayed by immunofluorescence using fluoresce isothiocyanate labeling. In addition, apoptosis was detected by morphological observation and flow cytometric analysis of DNA fragmentation.RESULTS:It was found that the two oligonucleotides directed against the coding region and the translation initiation of bcl-2 mRNA, combined respectively with daunorubicin, inhibited expression of bcl-2 protein, increased apoptosis in HL60 and K562 cells, and decreased IC50 of daunorubicin significantly (P＜0.05). Compared to the antisense oligonucleotide directed against the translation initiation of bcl-2 mRNA, the antisense oligonucleotide directed against the coding region showed stronger effects in the aspects of increasing the sensitivity of HL60 cells to daunorubicin (P＜0.05).CONCLUSIONS:These two antisense sequences in the translation initiation and the coding region of bcl-2 mRNA increased the sensitivity of HL60 and K562 cell lines to daunorubicin in a sequence-specific manner.  相似文献   

The mechanism of apoptosis induced by homoharringtonine in HL-60 cells     

CHEN Chun-yan  JIA Ji-hui  PAN Xiang-lin  ZHANG Qi  WANG Juan-dong  ZHOU Ya-bin 《园艺学报》2004,20(7):1183-1186

AIM: To study the signal transduction pathway of apoptosis initiation induced by homoharringtonine in HL-60 cells. METHODS: After establishing the model of apoptosis initiation induced by homoharringtonine in HL-60 cells, at the point of apoptosis initiation, molecular caspase-3, Bcl-2, Bax and Fas/FasL were measured with flow cytometry and transmission electron microscope. ERK2 and P38 expression in HL-60 cells were detected by using immunohistochemistry. RESULTS: The model of apoptosis initiation induced by homoharringtonine was established in HL-60 cells. At the point of apoptosis initiation, upregulation of caspase-3 and decrease in Bcl-2/Bax were observed. However, the expression of Fas/FasL did not significantly change. ERK2 expression decreased and P38 expression increased. CONCLUSIONS: Caspase-3, Bcl-2, Bax and mitogen activated protein kinase pathways were involved in signal transduction of apoptosis initiation induced by homoharringtonine in HL-60 cells.  相似文献   

Screening and Identification of Candidate Proteins Interacting with BmHSP60 in the Silkworm (Bombyx mori)     

DONG ZhanQi  JIANG YaMing  PAN MinHui 《中国农业科学》2019,52(2):376-384

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苜蓿地撂荒过程中土壤-微生物-胞外酶及化学计量的变化     

于宗恺  景煜都  刘励  刘小伟  张强  程杰  郭梁 《草地学报》2023,31(4):1115-1124

紫花苜蓿(Medicago sativa L.)作为优良修复草种在黄土高原广泛种植,然而随着农村人口迁移及土地利用变化,苜蓿人工草地大量弃置的问题已引起广泛关注。为研究苜蓿弃置草地土壤质量变化规律,本研究分析了不同弃置年限(0年、5年和10年)苜蓿草地土壤养分、微生物量、参与土壤碳氮磷(C,N,P)循环的胞外酶活性及其化学计量变化。结果表明：总体上,土壤和微生物C,N含量随弃置年限呈增加趋势,而C,N相关胞外酶活性和化学计量变化幅度较小;土壤和微生物P含量随弃置年限增加而显著降低,但P相关胞外酶活性及化学计量均有不同程度的增加。进一步分析发现：相较于其他土层,表层(0～20 cm)土壤C,N,P含量及其酶活性较高,其变化趋势与总体结果相似;亚表层土壤(20～40 cm)和(80～100 cm)深层土壤C,N,P含量及其酶活性呈先增后减趋势,且各指标较于表层土壤均降低40%～80%。相关分析表明弃置草地土壤由于P匮乏而逐步退化,可通过补施磷肥改善。  相似文献   

Irradiation Effect in C60 Films Induced by 120 keV H+ Ions     

ZHU Sheng -xing  YAO Jiang -hong 《保鲜与加工》2002,(7):57-59

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产单核细胞李斯特菌P60蛋白的可溶性表达     

吴仁蔚 《动物医学进展》2010,31(12)

以食品中分离到的L.mXFL0605株为试验菌株,PCR扩增得到iap全基因。将iap连接到pET-28a(+)载体进行原核表达,分别采用培养温度为25℃或37℃,IPTG浓度为5μg/mL或10μg/mL优化组合进行诱导。结果显示,当采用37℃培养和10μg/mLIPTG诱导时可以获得部分可溶性表达的p60,重组p60蛋白分子质量约60 ku。  相似文献   

一株无血凝性兔出血症病毒的分离鉴定及其衣壳蛋白VP60基因的克隆和序列分析   总被引：1，自引：0，他引：1  

田浪  王红宁  李建文  廖娟  张夏兰  周万蓉  王鸿宾 《畜牧兽医学报》2006,37(10):1078-1083

从临床病料中分离鉴定出1株无血凝性的致病性兔出血症病毒（RHDV），命名为Yaan-1。HA试验测得该毒株原代及经兔体传3代后的肝毒在25℃、37℃和4℃时均无血凝性；但在琼脂扩散试验和对流免疫电泳中均可见分离株与常规RHDV高免血清形成清晰的沉淀线；电镜观察可见30nm左右的病毒粒子。采用RT-PCR方法将Yaan-1株的衣壳蛋白VP60基因进行了克隆测序，序列分析表明VP60基因序列全长1740bp，编码579个氨基酸，测序结果提交GenBank（注册号为DQ069280），并与世界各国的常规RHDV分离株进行比较，结果表明核苷酸同源性为90．0％～98．0％，氨基酸同源性为94．1％～99．0％，氨基酸变异多发生在衣壳蛋白C、E区；同时对Yaan-1株的分子量、等电点、疏水性、跨膜区等分子结构特征进行了分析。本研究首次报道了无血凝性RHDV中国分离株，丰富了地方毒株资源，为明确我国地方株的分子流行病学，以及对VP60蛋白分子特征研究提供了新材料。  相似文献   

黄土坡面土壤性质随退耕时间的动态变化研究   总被引：4，自引：0，他引：4  

彭文英  张科利  杨勤科 《干旱区资源与环境》2006,20(5):153-158

退耕还林还草是控制水土流失和防治土壤退化的关键措施,黄土高原退耕还林还草从试验到推广已有几十年历史。该文通过对黄土高原地区退耕区的实地调查,测定不同地区不同退耕年限植被恢复区表层土壤的理化性质,分析黄土坡面土壤理化性质随退耕时间的动态变化规律。结果表明:随着退耕植被恢复时间的增长,土壤物理结构将日趋改善,土壤养分含量水平将逐渐的提高,并主要集中在植被恢复10~20年期间,20年后,尤其是30年后,土壤理化性质较为稳定,而且,植被维护的好坏往往影响其稳定性。同时,水热条件较好的安塞地区土壤理化性质随退耕时间的改善程度更明显,而水热条件较差的皇甫川流域土壤理化性质随植被类型和植被恢复程度的影响更为显著。结果可为退耕的环境影响评价预测以及土地利用的调控提供科学依据。  相似文献   

Lethal effect of VEGFR₂shRNA on HL60 cells in vitro using lentiviral vector     

GUO Hai-xia  LI Wen-yi  XU Ling  SU Hao-bin  LI Yang  XIA Yan  LIANG Li-yang 《园艺学报》2007,23(6):1053-1057

AIM: To look for harmfulless anti-leukemia drug with selective high performance, lethal effect of small hairpin RNA (shRNA) on VEGFR₂ gene expression of tumor cell line HL60 in vitro.METHODS: The most effective VEGFR₂ siRNA was designed and screened. The shRNA oligo was designed and pU6/VEGFR₂ entry clone was constructed. HL60 was transfected transiently and vascular endothelial growth factor receptor 2(VEGFR₂) expression was tested with MTT assay, RT-PCR and Western blotting. The expression clone was constructed and cotransfected with ViraPowerTM Packaging Mix into 293FTTM cells to produce Lentiviral vectors harboring Lenti6/shVEGFR₂. The virion supernatant was added into HL60 cells and VEGFR₂ gene inhibitory effect was determined. RESULTS: The inhibitory rates of VEGFR₂ siRNA c were high. VEGFR₂ expression in HL60 was inhibited by using pU6/VEGFR₂ entry clone constructed with shRNA and pENTRTM/U6. For HL60 cells, the inhibitory rate was 84.9%. The expression of VEGFR₂ mRNA and protein decreased significantly. 48 hours after transfection of pU6/shVEGFR₂ entry clone and transduction of Lenti6/shVEGFR₂ expression clone, the cell inhibitory rates were similar. Cell growth inhibitory rate of entry clone descended rapidly after this time point, the expression clone changed slowly, reaching the peak at 96 hours, dropped slightly, having no significance deviation. CONCLUSION: in vitro, VEGFR₂ shRNA using lentiviral vector blocks VEGF/VEGFR₂ self-secretion in HL60 cells, which inhibits leukemia development.  相似文献