外源NO及反向调控PEG胁迫下苜蓿萌发种子抗氧化酶及其同工酶动态的研究

以紫花苜蓿为材料,用一氧化氮供体硝普钠(SNP)及一氧化氮清除剂c-PTIO对苜蓿种子进行浸种处理,采用分光光度法和同工酶电泳技术来研究外源NO及反向调控对PEG胁迫下紫花苜蓿抗氧化酶活性及其同工酶的影响,并探讨NO调控苜蓿种子耐旱性的生理机制。结果表明:PEG胁迫下外施0.1 mmol·L^-1 SNP,第6天时较PEG处理POD活性降低了32.72%;第4天时SOD、CAT活性较PEG处理升高了10.48%、23.60%,有效缓解了PEG对紫花苜蓿萌发中种子的氧化损伤,提高其抗氧化能力。PEG胁迫下添加 c-PTIO抑制了苜蓿萌发期的抗氧化系统活性。从同工酶的谱带数量和强弱来看,POD同工酶各区带活力均随PEG胁迫时间的延长而增加,在第2天酶带只有1条,而第4天酶带呈现9条;SOD和CAT同工酶表达量变化不显著,但酶带强弱有一定变化,S3酶带随处理时间的延长表达量逐渐减弱;CAT同工酶谱带则一直保持2条带,无明显强弱变化。因此,外源NO在PEG胁迫下紫花苜蓿萌发中抗氧化酶快速响应并在维护氧自由基代谢平衡中起重要保护作用。     

垂叶榕瘿花发育特性的初步研究

研究榕属植物瘿花发育特性是理解榕树/榕小蜂协同进化内在机制的重要内容。本文解析了垂叶榕隐头花序伴随瘿花发育的 5 个发育时期，采用同工酶电泳的方法比较了瘿花与正常雌花同工酶（包括过氧化物酶、过氧化氢酶、淀粉酶和酯酶）谱带的差异，采用扫描电镜对比了瘿花壁与授粉后雌花子房壁的差异。结果表明，瘿花被榕小蜂产卵以后，至少启动了一个与消除过氧化物有关的酶；而且，瘿花子房壁结构疏松，内含物小而少，雌花子房壁结构致密且内含物多而大，说明瘿花发育所消耗的营养物质大于正常雌花发育的消耗。研究结果支持造瘿生物汇集营养与植物防御行为的互利假说。     

银鲳不同组织中4种同工酶的表达差异

采用聚丙烯酰胺凝胶电泳技术,分析了银鲳(Pampus argenteus)脾脏、肝脏、肌肉、心脏、肾脏等5种组织中酯酶(EST)、乳酸脱氢酶(LDH)、谷氨酸脱氢酶(GDH)、乙醇脱氢酶(ADH)等4种同工酶的表达模式,并对各种同工酶的酶谱进行了分析。结果表明:这4种同工酶在银鲳5种组织中的分布均存在一定的组织特异性,其与各组织的生理机能密切相关。银鲳4种同工酶共记录出61条酶带,其中EST被检测出的酶带数量最多也较复杂,ADH同工酶酶带数量最少,只有6条酶带被检测到,LDH和GDH分别检测到16条和9条酶带;组织特异性主要表现在位点表达和酶活性强弱不同这两个方面,GDH1和ADH2只在肝脏中表达。     

偶氮类色素胭脂红对泥鳅组织酯酶同工酶表达的影响

采用肌肉注射法进行染毒,运用聚丙烯酰胺凝胶电泳法研究胭脂红在不同注射剂量、不同染毒时间对泥鳅肝脏、心脏、脾脏、肌肉酯酶同工酶表达的影响。试验结果表明,经一定剂量的胭脂红注射后,泥鳅酯酶同工酶在脾脏中表达最强,肝脏和心脏次之,肌肉最弱,其中脾脏的表达随时间、浓度呈减弱趋势,其余组织则呈先增强再减弱最后增强的趋势。     

低能Ar+注入樱桃萝卜点点红种子后的生物学效应

选取樱桃萝卜点点红为材料,对低能Ar+离子注入其干种子后的生物学效应进行了研究。考察了其发芽率、成活率与低能Ar+注入剂量的关系,对低能Ar+注入点点红种子后其过氧化物酶(POD)的活性进行了测定,并对POD酶谱及酯酶(Est)同工酶酶谱进行分析。研究结果表明,不同剂量的低能Ar+注入都会引起种子发芽率、成活率及不同阶段的生长和发育产生变异;在1×1017Ar+/cm2与3×1017Ar+/cm2剂量之间点点红种子的发芽率随注入剂量的增加呈现出“马鞍型”曲线的变化趋势;成活率的变化规律与发芽率的变化规律基本一致;低剂量注入时,其POD活性随剂量的增加而升高;高剂量注入时,其POD活性随剂量的增加而降低。同工酶图谱中,POD在2.5×1017Ar+/cm2和3.0×1017Ar+/cm2增加一条酶带,且1.5×1017Ar+/cm2和3.0×1017Ar+/cm2高剂量注入时有缺失现象;酯酶(Est)在1.5×1017Ar+/cm2和3.0×1017Ar+/cm2剂量注入时酶带数增加,且变深。     

Geographical distribution of allozyme patterns in shallot (Allium cepa var. ascalonicum Backer) and wakegi onion (A. × wakegi Araki)

Summary Shallot and wakegi were collected in the main islands of Indonesia, and in Japan, Korea, Taiwan, Malaysia, Thailand and Bangladesh. Five isozyme resolutions, phosphoglucomutase (PGM), glutamate oxaloacetate (GOT), glutamate dehydrogenase (GDH), esterase (EST) and peroxidase (POX) were employed for demonstrating inter-and intraspecific differences. A dendrogram separated 189 collected accessions into 25 types of wakegi onion and 18 types of shallot. All accessions of Japan, Korea and Taiwan were determined to be wakegi onion, whereas those of Bangladesh, Malaysia and Thailand were shallot. Twenty-six out of 165 Indonesian accessions indicated wakegi onion distribution in Sumatra, West Java province and in Sulawesi Island. This confirmed that there is mixed-cultivation of the two Allium species with no distinction made between them. Japan and Indonesia had respectively 12 and eight unique types of wakegi onion, while Korea had only one type. West Java showed the most various type of wakegi onion, whereas East Java had many types of shallot. Shallots collected from Bangladesh were distinetly different from those of South East Asian types.     

Genetic control of alcohol dehydrogenase, malate dehydrogenase, and phosphoglucomutase isozymes in lima bean (Phaseolus lunatus L.)

A suitable electrophoretic separation method for alcohol dehydrogenase (ADH). malate dehydrogenase (MDH). and phosphoglucomutase (PGM) from P. lunatus has been developed. Two loci (Adh-2 and Pgm-2) showed codominant inheritance and fitted Mendelian ratio. ADH isozyme banding patterns indicate a dimeric quaternary structure. while those of PGM were in agreement with a monomeric nature. The cytoplasmic location of two MDH isozymes (Mdh-1 and Mdh-2) selectively inactivated by homogenization in an ascorbic acid solution was demonstrated. However. distorted ratios were observed for Mdh-2 segregation. On the basis of MDH isozyme banding patterns observed in five progeny families, il is suggested that this enzyme system is a dimeric protein encoded by at least three codominant genes (Mdh-1 .Mdh-2 and Mdh-3). Joint segregation tests between pairs of segregating loci (Adh-2, Mdh-2, and Pgm-2) indicated that each of them is inherited independently.     

Characterization of isozyme variation in walnut(Juglans regia L.)

Summary Four leaf enzymes malate dehydrogenase (MDH), 6-phosphogluconate dehydrogenase (6PGD), peroxidase (PX) and aspartate aminotransferase (AAT) of 17 walnut cultivars and two pollen enzymes malate dehydrogenase (MDH) and 6-phosphogluconate dehydrogenase (6PGD) of 15 walnut cultivars were analysed using horizontal starch gel electrophoresis. Walnut cultivars of different origin exhibited different numbers of electrophoretic bands and also different relative mobility. Different activity levels and phenotypic groups were detected in studied enzyme systems. Pollen enzymes revealed higher variability than enzymes extracted from the leaves. 15 walnut cultivars were classified into 10 malate dehydrogenase phenotypic groups and 14 6-phosphogluconate dehydrogenase phenotypic groups based on pollen analyses. 17 cultivars were classified into 9 peroxidase phenotypic groups and 7 6-phosphogluconate dehydrogenase phenotypic groups based on analyses of leaves. All of the 15 walnut cultivars could be identified and distinguished with electrophoretic analyses of MDH and 6PGD from the pollen while only 10 cultivars were distinguishable with analyses of 6PGD and PRX from the leaves. No variability useful for cultivar identification was observed in MDH and AAT from the leaves.     

几个家蚕品种不同性别血淋巴酯酶同工酶的比较

用聚丙烯酰胺等电聚焦电泳,分析了不同血统和化性的九个品种的家蚕(Bombyxmori)血淋巴酯酶同工酶(EST).结果表明,所有的品种五龄盛食期幼虫都呈现相似的酶谱,可区分为四个区带(ESTⅠ、Ⅱ、Ⅲ和Ⅳ),共出现18条带,带的数目和酶活强度随品种而异.在五个品种中的Ⅲ-3及四个品种中的Ⅱ-2出现了伴性现象,Ⅲ-3伴随雄性、Ⅱ-2伴随雌性出现.     

Inheritance of new genetic markers in lentil (Lens Miller)

Summary We report on the inheritance of 11 morphological markers and 17 isozymes in lentil (Lens culinaris). The monogenic inheritance of 11 morphological markers and 11 isozymes is confirmed. The inheritance of six isozymes (Aco-2, Enp, Est-3, Est-4, Lap-3, and Mdh-m) is reported for the first time in lentil. This brings the total number of described genes in lentil to 78. Cases of disturbed segregation were more frequent than expected by chance. It is suggested that disturbed segregation was in most cases caused by linkage with a piece of chromosome that showed preferential elimination in crosses between Lens culinaris ssp. odemensis and other subspecies. The prevalence of disturbed segregation in crosses with Lens culinaris ssp. odemensis could limit the usefulness of this subspecies in genetic and linkage studies.