松南海坨子—大布苏地区泉四段— 姚家组层序地层研究

根据工区内现有的钻井、测井和地震资料,应用以多级次基准面旋回为参照面的高分辨层序地层学理论与研究方法,对松辽盆地南部海坨子—大布苏地区的泉四段—姚家组地层进行了详细的层序地层研究,共识别出5个长期基准面旋回（相当于三级层序）,9个中期基准面旋回（相当于四级层序）,建立了研究区的层序划分方案,在连井剖面的层序地层对比基础上,建立了该区的地层格架,并对层序构成特征进行了分析,研究了储集层在层序格架内的分布规律,揭示出浊积砂体和三角洲前缘相的分流河道形成于基准面上升期,三角洲前缘相的河口坝、远砂坝和席状砂沉积形成于基准面下降期,指出浊积砂体和三角洲前缘相的远砂坝、席状砂沉积是研究区形成岩性油气藏的有利储集体。     

盐胁迫对番茄同工酶基因表达的影响

分析了普通番茄（Lycopersicumesculentum）在NaCl胁迫下酯酶（EST）和过氧化物酶（PRX）同工酶的变化，考察了盐胁迫对10个同工酶位点21个等位基因在特定组织中表达的影响。发现许多EST和PRX等位基因在盐胁迫下表达，产生盐诱导同工酶；另有些等位基因的表达受盐抑制，它们在盐胁迫下的表达活性显著减弱或消失。实验表明，EST和PRX同工酶表达的变化与番茄对盐胁迫的遗传适应性有密切关系。     

Microbial Diversity in Nankai Trough Sediments at a Depth of 3,843 m

Dense populations of bivalves, primarily Calyptogena sp., were observed at cold seeps of the Nankai Trough. Bacterial input to the sediment was estimated through determination of phospholipid ester-linked fatty acid (PLFA) and DNA profiles. Results indicated a bacterial biomass of 10⁹ cells (g dry wt)^-1 while individual fatty acid profiles revealed a predominance of monounsaturated fatty acids, mainly 18:1 isomers. The presence of these fatty acids can be interpreted to reflect a response to low temperature and a predominance of psychrophilic bacteria. DNA fragments encoding bacterial ribosomal RNA small-subunit sequences (16S rDNA) were amplified by the polymerase chain reaction method using DNA extracted directly from the sediment samples. From the sequencing results, at least 19 kinds of bacterial 16S rDNAs related to mostly the Proteobacteria and a few gram-positive bacteria were identified. These results suggest that the bacterial community in the Nankai Trough sediments consists of mainly bacteria belonging to the Proteobacteria , , and subdivisions. Bacteria belonging to the and subdivisions, which are known to include epibiont and sulfate reducing bacteria, respectively, were mostly detected in the sediment obtained from inside the area of the Calyptogena community, and the -Proteobacteria may function to supply reduced sulfur to bacterial endosymbionts of Calyptogena.     

魁蚶线粒体16S rRNA和COI基因片段序列测定及其应用前景

魁蚶（Ｓｃａｐｈａｒｃａｂｒｏｕｇｈｔｏｎｉｉ）是蚶科贝类的一种大型经济种类，主要分布于我国、日本和朝鲜半岛及俄罗斯东南部沿海。在我国，主要分布于辽宁、河北和山东沿海，生活在３～５０ｍ（多为２０～３０ｍ）水深的软泥或泥沙质海底，是我国北方沿海重要的经济贝类之一。但但有有关关其其自自然然群群体体的的遗遗传传变变异异及及群群体体间间遗遗传传分分化化等等方方面面的的研研究究不不多多 ;;同同时时，，作作者者和和日日本本研研究究者者发发现现，，中中国国、、韩韩国国和和日日本本魁魁蚶蚶群群体体在在形形态态和…     

中华齿米虾胰蛋白酶基因的研究

以中华齿米虾(Neocaridina denticulata sinensis)基因组DNA为模板,根据胰蛋白酶基因保守序列设计简并引物,利用PCR技术获得一个基因。序列分析表明此基因与已报道的凡纳滨对虾(Litopenaeus vannamei)胰蛋白酶基因有较高的相似度,序列中包含一个内含子和两个不完整的外显子,编码182个氨基酸残基。该氨基酸序列与凡纳滨对虾胰蛋白酶氨基酸序列的相似度为83.5%;含有胰蛋白酶所特有的His、Asp和Ser组成的活性三联体、决定胰蛋白酶底物专一性的Asp、底物结合部位的G1y残基。综合分析认定该基因为胰蛋白酶基因片断。将其氨基酸序列与报道的其他动物胰蛋白酶氨基酸序列进行了系统进化分析。系统进化分析的结果与现有以表型特征为依据的虾分类结果是一致的。     

6-磷酸山梨醇脱氢酶(gutD)基因克隆、测序和表达

本研究根据6-磷酸山梨醇脱氢酶基因(gutD)两端序列设计引物，以假单胞杆菌(Pseudonmonas XM)的总DNA为模板通过PCR的方法克隆gutD基因并进行序列分析，将克隆得到的gutD基因与原核表达载体pBV220连接并转化大肠杆菌(Escherichia coli)JM101后检测其蛋白表达及菌株生长耐盐性。     

地层学的发展推动油气地质理论研究的进步

自上个世纪50年代以来,地层学经历了彻底的变革,逐渐由“相模式”、“沉积体系”、“地震地层学”发展到目前的“层序地层学”,形成高分辨率层序地层学和事件地层学的理论体系和研究方法。文章围绕层序地层学、高分辨率层序地层学基本方法及理论体系,与含油气系统相关关系进行了讨论。     

用16S rRNA基因的内切酶图谱快速鉴别几种对虾病原菌

坎普氏弧菌是青岛海洋大学生物系微生物实验室于１９８９－１９９０年自对虾养殖场中国对虾红腿病心脏及血淋巴中分离并鉴定的菌株，副溶血菌和溶藻胶弧菌两菌株于１９９４年９月得自中国科学院微生物研究所，为建立快速、准确的中国对虾病原菌的诊断技术，根据几种细菌的１６ＳｒＲＮＡ基因的序列，设计并合成该基因的多聚酶反应的引物ＰＬ１和ＰＬ２。并用该对引物分别从坎普氏弧菌、副溶血弧菌和溶藻胶弧菌的ＤＮＡ要品中扩增出分     

Diagnosis of iridovirus in large yellow croaker by PCR

A rapid and sensitive PCR-based method for the detection of the large yellow croaker iridovirus(LYCIV) is described,which involves the amplification of a 295 bp fragment of the LYCIV ATPase gene from DNA isolated from naturally infected fish spleen.Sequencing of LYCIV ATPase gene fragment showed it shared 100% nucleotide sequence homology with the corresponding region of the ATPase gene of red sea bream iridovirus(RSIV) and sea bass iridovirus(SBIV),suggesting that LYCIV was homologous with RSIV and SBIV at least in part of the gemone.The specificity and sensitivity of the PCR procedure were tested on the iridovirus-infected fishes,the expected fragment was detected from spleen DNA samples of infected fishes,whereas no fragments were amplified from healthy fish spleen DNA,white spot syndrome baculoviruses(WSBV) DNA and pseudorabies virus(PRV) DNA.Detection limit of this method was 10^-7 ng positive plasmid DNA containing target sequence,equal to about 100 virions.In the infected experiment,first positive detection(1/4) appeared at Day 3 post-infection,all fish(4/4) tested positive at Day 7,however obvious symptoms were observed at Day 8,so LYCIV infection could be detected prior to the appearance of obvious symptoms.These results indicate that this PCR method could be used for early,rapid and specific detection of LYCIV infection.