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111.
Pei-Wen Chiang SuQing Wang Paul Smithivas Woo-Joo Song Saravanan Ramamoorthy Joseph Hillman Sheryl Puett Margaret L. Van Keuren Eric Crombez Arun Kumar Thomas W. Glover Diane E. Miller Chun-Hui Tsai C.Clare Blackburn Xiao-Ning Chen Zhiguang Sun Jan-Fang Cheng Julie R. Korenberg David M. Kurnit 《Genomics》1996,34(3):328
112.
Geneticdivergenceanalysiswasconductedbasedonperformanceof12quantitativetraitsin85sunflowerinbredlines,tostudyitseffectivenessinpredictingyieldheterosisofthe72hybridsfromthem.Resultsshowedthatlinearregressionmodelfittherelationshipbetweenheterosisofseedoilcontentandgeneticdistance,andquadraticregressionequationtherelationshipbetweengrainyieldheterosisandgeneticdistance,whichcanbeusedinpredictingheterosisfromtheparentperformances.Clusteranalysiswaseffectivetocertainextent,butitsutilizationshouldbelimited.Grainyieldandoilcontentcanbeimprovedsimutaneouslyaccordingtotherelationsbetweengeneticdivergenceandtheheterosisofthesetwotraits. 相似文献
113.
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116.
棉铃虫病毒杀虫乳悬剂的生产及其药效试验 总被引:5,自引:1,他引:4
成功研制出棉铃虫病毒(NPV)杀虫乳悬剂,改进了生产工艺和设备,建立了棉铃虫的室内品系,提高了生产效率,建立了产品的检测方法,提高了产品质量,促使棉铃虫病毒杀虫剂商品开发获得成功。大田试验证明,病毒乳悬剂的防治效果,相当于当前推广的化学农药,优于原病毒可湿性粉剂。相同剂量(0.53一1.07×10(10)PIB/公顷)的病毒乳悬剂可使虫口平均减退91.7%,而病毒可湿性粉剂为83.7%。 相似文献
117.
用苯甲基磺酰氟(PMSF)和H_2Se相继处理铜锌超氧化物岐化酶(Cu,Zn-SOD),将酶分子中的丝氨酸(Ser)转化为硒代半胱氨酸(SeCys),从而引入了谷胱甘肽过氧化物酶(GPX)的催化基团,使其在SOD酶活性大部分保留的情况下,具有GPX活性,其GPX活力是PZ51活力的30倍。研究了双功能酶的最佳制备条件,包括PMSF的剂量、反应最适温度及H_2Se处理时间等,并用电子能谱、DTNB等方法测定了双功能酶的硒含量;测定了双功能酶对不同底物的米氏常数及双功能酶的荧光光谱、紫外吸收光谱及稳定性。 相似文献
118.
Gloria Giacomini Santo V. Nicosia Beatriz O. Saunders Caroline Fultz X. Sun Valerio M. Jasonni 《In vitro cellular & developmental biology. Animal》1995,31(4):300-309
Summary The ovarian mesothelium (OM) represents the tissue of origin of ovarian epithelial cancer. To gain insight into the regulation
of this tissue, OM organoids and submesothelial ovarian stromal cells (SC) were isolated from New Zealand White rabbits by
a stepwise tissue dispersal technique, while granulosa cells (GC) were aspirated from mature follicles (14±4 groups/animal).
OM and SC dispersal were sequentially accomplished by: a) 1-h incubation in collagenase type I (300 U/ml), gentle scraping
of the ovarian surface, and 1 g sedimentation of OM organoids (equivalent to 0.93±0.40 × 106 cells/animal) on 5% bovine serum albumin (BSA); b) 2-h incubation in pronase-collagenase (0.5%–300 U/ml) under periodical
resuspension and gentle scraping of SC (1.40±0.25 × 106/animal) from OM-denuded ovaries. After a week-long in vitro expansion, OM cells (OMC) were cultured alone and with SC or
GC within monocameral vessels or bicameral transfilter vessels in serumless, fibronectinrich (4μg/ml) HL-1 medium. After 7
d of contact cell-cell interaction, cytokeratin-positive OMC became surrounded by fibroblastoid, vimentin-positive SC or by
cytokeratin and vimentin-weakly positive GC. Filter-bound OMC humorally interacting with underlying SC or GC displayed a biphasic,
epithelioid and spindle, morphology with universal cytokeratin expression. Bromo-2′-deoxyuridine (BrdU) immunoperoxidase revealed
mean cell proliferation indices of 14.88% for OMC cultured alone, 11.21% and 19.39% for OMC cultured with GC or SC in monocameral
dishes, and 15.25% or 22.47% for OMC cultured in bicameral vessels over GC or SC, respectively. This model provides an experimental
tool for investigating the unexplored role of stromal-mesothelial interaction in OM pathobiology. 相似文献
119.
Cloning and functional characterization of LCR-F1: a bZIP transcription factor that activates erythroid-specific,human globin gene expression.
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DNase I hypersensitive site 2 (HS 2) of the human beta-globin Locus Control Region (LCR) directs high level expression of the beta-globin gene located 50 kilobases downstream. Experiments in cultured cells and in transgenic mice demonstrate that duplicated AP1-like sites in HS 2 are required for this powerful enhancer activity. A cDNA clone encoding a basic, leucine-zipper protein that binds to these sites was isolated and designated Locus Control Region-Factor 1 (LCR-F1). This protein is a member of a new family of regulatory factors that contain a 63 amino acid ''CNC domain'' overlapping the basic region. This domain is approximately 70% identical in the Drosophila Cap N Collar (CNC) protein, NF-E2 and LCR-F1. LCR-F1 transactivates an HS 2/gamma-globin reporter gene over 170-fold in transient transfection experiments specifically in erythroid cells. These results suggest that LCR-F1 may be a critical factor involved in LCR-mediated, human globin gene expression. 相似文献
120.
Cloning and DNA sequencing of the dextranase inhibitor gene (dei) from Streptococcus sobrinus. 总被引:3,自引:3,他引:0
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Some dextranase-deficient (Dex-) mutants of Streptococcus sobrinus UAB66 (serotype g) synthesize a substance which inhibits dextranase activity (S.-Y. Wanda, A. Camilli, H. M. Murchison, and R. Curtiss III, J. Bacteriol. 176:7206-7212, 1994). This substance produced by the Dex- mutant UAB108 was designated dextranase inhibitor (Dei) and identified as a protein. The Dei gene (dei) from UAB108 has been cloned into pACYC184 to yield pYA2651, which was then used to generate several subclones (pYA2653 to pYA2657). The DNA sequence of dei was determined by using Tn5seq1 transposon mutagenesis of pYA2653. The open reading frame of dei is 990 bp long. It encodes a signal peptide of 38 amino acids and a mature Dei protein of 292 amino acids with a molecular weight of 31,372. The deduced amino acid sequence of Dei shows various degrees of similarity with glucosyltransferases and glucan-binding protein and contains A and C repeating units probably involved in glucan binding. Southern hybridization results showed that the dei probe from UAB108 hybridized to the same-size fragment in S. sobrinus (serotype d and g) DNA, to a different-size fragment in S. downei (serotype h) and S. cricetus (serotype a), and not at all to DNAs from other mutans group of streptococci. 相似文献