垦稻11号良种良法技术研究

通过对垦稻11号进行不同插期、不同密度和不同施肥量级的试验,找出其在我场大田生产上推广繁育的合理栽培方法和模式。试验结果表明,垦稻11号的最适宜插秧时间是5月13～23日,插秧规格30 cm×13 cm为宜,每穴3～5苗,施肥量应以处理2为准,N∶P∶K比例为2∶1.05∶0.65。     

工业化大豆蛋白7S和11S组分分离技术研究进展

该文围绕目前工业化生产11S和7S组分的分离技术成果,结合实验室的分离技术(Guo法),比较了各种分离方法的差异.结果表明:分离提取技术利用的原理几乎均建立在"碱溶酸提"和"冷沉"作用基础之上.Wu首次成功地进行了7S和11S的工业化分离,之后的研究多是对此方法的改进和修饰.而Guo法是唯一采用中性条件抽提的工业化分离方法,在节省了原料碱的同时,避免了蛋白的变性.同时,该文提出了目前工业化生产大豆组分蛋白中存在的问题,虽然不断在加工方式上进行改进,但仍存在步骤复杂、产率低、生产成本高等方面的问题,因此作者进一步对实现工业化分离大豆组分蛋白提出了需要改进和努力的方向.     

马铃薯新品种——‘鄂马铃薯11’的选育

‘鄂马铃薯11’是湖北恩施中国南方马铃薯研究中心以‘南中552’(4x)作母本、‘DY4-2-10’(2x)为父本,通过有性杂交经过育种程序选育而成,2013年4月通过湖北省农作物品种审定委员会审定,审定编号为:鄂审薯2013001。该品种属中晚熟品种,2010²011年参加湖北省马铃薯品种区域试验,平均产量1 920 kg/667m2,比对照‘米拉’增产11.8%。该品种适于湖北省海拔700 m以上地区种植,属鲜食、加工兼用型品种。     

Immunohistochemical study on changes in gill Na+/K+-ATPase α-subunit during smoltification in the wild masu salmon, Oncorhynchus masou

Changes in immunoreactivity of Na⁺/K⁺-ATPase 11w528r/xxlarge945.gif" alt="agr" align="BASELINE" BORDER="0">-subunit in gill sections of wild masu salmon (Oncorhynchus masou) during the parr-smolt transformation (smoltification) were compared with changes in gill Na⁺/K⁺-ATPase specific activity. Gill Na⁺/K⁺-ATPase specific activity increased from April and peaked in May. Immunohistochemical analysis, using an antiserum against a synthetic oligopeptide based on the conserved region of the Na⁺/K⁺-ATPase 11w528r/xxlarge945.gif" alt="agr" align="BASELINE" BORDER="0">-subunit, revealed that immunoreactivity was confined to chloride cells in the surface layer of primary lamellae and the proximal end of secondary lamellae. The size and number of these cells increased gradually from February to May; however, the number of chloride cells of the secondary lamellae decreased in May. These data suggest that the synthesis of Na⁺/K⁺-ATPase and the proliferation of chloride cells occur prior to the elevation of enzyme activity. Moreover, it is likely the proliferation and hypertrophy of chloride cells on primary lamellae prepare smolts for entry into seawater and migration in the ocean.     

番茄果实特异性启动子2A11的基因克隆及功能研究

采用巢式PCR技术从番茄基因组DNA克隆到长度1.3kp的果实特异性2A11启动子基因。序列分析表明,克隆到的基因序列2A11启动子转录起始位点上游的621bp处缺失了已报道的番茄2A11启动子基因（GenBank ID M87659,1993）序列中的“tatattgttaacttcttgttgaattaaagcaat”片段,其同源性为61%,登入GenBank,ID号为DQ453963;构建植物表达载体pCAMBIA2A11,用农杆菌介导侵染番茄果实,GUS基因瞬间表达结果表明,该2A11启动子基因具有驱动GUS基因在番茄果实中特异性表达的功能。研究结果表明成功地获得2A11果实特异性启动子基因,为下一步转基因番茄口服疫苗的研制奠定了一定的基础。     

高蛋白高产大豆新品种石豆11号的选育

石豆11号是由石家庄市农林科学研究院以化诱446为母本,冀豆4号为父本经有性杂交选育而成。2014-2015年参加河北省夏播大豆区域试验,平均产量3 093.9 kg·hm~(-2),较对照冀豆12增产2.51%。2016年参加河北省夏播大豆生产试验,平均产量3 108.0 kg·hm~(-2),较对照冀豆12增产0.87%。2017年通过河北省农作物品种审定委员会审定,准予推广。石豆11号的主要特点是高蛋白(45.79%)、高产、抗倒伏,适宜在河北省中南部夏播种植。     

Identification and establishment of sorting method for isolating CD11b+ myeloid cells in human hepatic metastases from colorectal cancer

AIM: To establish a method for obtaining specific cells in solid tumor tissue by sorting of CD11b⁺ myeloid cells in hepatic metastases from colorectal cancer.METHODS: Tumor tissues were prepared into single cell suspension by mechanical method combined with enzyme digestion, and then the CD11b⁺ myeloid cells were isolated by flow cytometry. The sorted cells were identified by immunocytochemistry. The viability and morphologiy of the sorted cells were evaluated by Giemsa and Typan blue staining. The cell purity was evaluated by flow cytometry.RESULTS: Sufficient numbers of CD11b⁺ cells with high purity were isolated by sorting with flow cytometry from the single cell suspension prepared by mechanical and enzyme digestion. The purity of the cells was confirmed by statistical analysis (P<0.05). The positive rates of the cells before and after sorting were significantly different (P<0.01). The positive cells were verified by immunocytochemical method. Meanwhile, the sorted cells had complete morphology and good activity.CONCLUSION: The CD11b⁺ myeloid cells in solid tumor tissue can be isolated by flow cytometry from the machine-enzyme digestion suspension with high purity, good activity and complete morphology.     

AsKC11, a Kunitz Peptide from Anemonia sulcata,Is a Novel Activator of G Protein-Coupled Inward-Rectifier Potassium Channels

(1) Background: G protein-coupled inward-rectifier potassium (GIRK) channels, especially neuronal GIRK1/2 channels, have been the focus of intense research interest for developing drugs against brain diseases. In this context, venom peptides that selectively activate GIRK channels can be seen as a new source for drug development. Here, we report on the identification and electrophysiological characterization of a novel activator of GIRK1/2 channels, AsKC11, found in the venom of the sea anemone Anemonia sulcata. (2) Methods: AsKC11 was purified from the sea anemone venom by reverse-phase chromatography and the sequence was identified by mass spectrometry. Using the two-electrode voltage-clamp technique, the activity of AsKC11 on GIRK1/2 channels was studied and its selectivity for other potassium channels was investigated. (3) Results: AsKC11, a Kunitz peptide found in the venom of A. sulcata, is the first peptide shown to directly activate neuronal GIRK1/2 channels independent from Gi/o protein activity, without affecting the inward-rectifier potassium channel (IRK1) and with only a minor effect on K_V1.6 channels. Thus, AsKC11 is a novel activator of GIRK channels resulting in larger K⁺ currents because of an increased chord conductance. (4) Conclusions: These discoveries provide new insights into a novel class of GIRK activators.     

不同启动子在水稻悬浮细胞中诱导外源基因的表达

为进一步提高外源基因在水稻悬浮细胞中的表达水平,以花椰菜花叶病毒(Ca MV)35S启动子为对照,克隆了玉米泛素蛋白启动子(Ubi)、水稻肌动蛋白启动子(Actin)以及水稻Oscc1启动子,以GFP为报告基因,通过启动子串联的方式,构建了10个植物表达载体:p CAMBIA 1304 35S-GFP、Ubi-GFP、Actin-GFP、Oscc1-GFP、35S/Ubi-GFP、35S/Actin-GFP、35S/Oscc1-GFP、Ubi/Actin-GFP、Ubi/Oscc1-GFP、Actin/Oscc1-GFP,采用根瘤农杆菌介导的方法,将表达载体导入日本晴胚性愈伤,经悬浮培养分别获得转基因的悬浮细胞系,利用荧光显微镜、酶标仪检测GFP荧光强度,用Western blot检测GFP蛋白质的表达水平。结果发现串联启动子明显强于单个启动子驱动的GFP蛋白质表达水平。在10个表达载体中,35S/Ubi、Ubi/Actin和Ubi/Oscc1是3种优化的启动子组合,其中Ubi/Oscc1串联启动子驱动GFP的表达水平最高,约为对照35S启动子的3倍。     

Q型烟粉虱为害对不同辣椒品种叶绿素及营养物质的影响

为明确辣椒品种对烟粉虱的抗性机制,以不同抗性程度的辣椒为试验材料,研究了其受Q型烟粉虱危害后体内生理指标的变化。结果显示,Q型烟粉虱危害后,辣椒叶绿素和可溶性糖含量均较对照(未接虫)增加,其中抗性品种(苏椒5号、新研988椒王)叶绿素含量增加显著(P0.05);可溶性糖含量以抗性品种增幅最大(P0.05),中抗品种(萧新九号、湘辛三号)次之(P0.05),感虫品种(港上红尖椒、大禹牛角王)的增幅最小。烟粉虱危害后所有参试品种除中抗品种湘辛三号外,其余品种的可溶性蛋白含量均较对照降低;所有参试品种的游离脯氨酸含量均显著降低(P0.05),感虫品种港上红尖椒、大禹牛角王的游离脯氨酸含量均显著高于高抗及中抗品种(P0.05)。因此,辣椒品种对Q型烟粉虱的抗性强弱与叶片叶绿素含量、可溶性糖含量、游离脯氨酸含量有关,而与可溶性蛋白含量无明显相关。