小麦耐盐细胞系脯氨酸SOD酶核酸和蛋白质合成动态分析

对已筛选出的小麦耐盐细胞系的耐盐稳定性进行有关生理、生化分析。结果表明：耐盐细胞系脯氨酸含量不仅稳定,而且高于对照;ＳＯＤ活性在耐盐系增加,耐盐系对一定的盐浓度损伤ＤＮＡ修复能力大于对照系,耐盐系ＲＮＡ和蛋白质合成量分别是对照的５．４和４．５倍,并对小麦耐盐性的有关问题进行了讨论。     

细胞分裂素对大豆叶片衰老过程中蛋白激酶基因表达的影响

利用真核生物催化丝氨酸／苏氨酸残基磷酸化的蛋白激酶ＶＩ和Ⅷ保守区设计兼并引物,进行ＲＴ－ＰＣＲ扩增反应,研究大豆叶片衰老过程中蛋白激酶基因表达的变化及外源细胞分裂素处理的作用。结果表明人工合成的细胞分裂素－６ＢＡ预处理很可能在转录水平上正向调节一些蛋白激酶基因的表达,而诱导衰老处理则起负调控作用。     

黄旗海产卤虫(Artemiapathenogenetica)成虫干片蛋白质、脂肪酸、氨基酸和矿物质的分析

对黄旗海产卤虫（Ａｒｔｅｍｉａｐａｔｈｅｎｏｇｅｎｅｔｉｃａ）成虫干片的蛋白质、脂肪酸、氨基酸和部分矿物质进行了初步分析．结果表明,粗蛋白含量为５４．１４％,脂肪酸中亚麻酸的含量为１５．０７％,蛋白质中的１７种氨基酸和部分矿物质的含量也很丰富,由此说明从盐碱湖中开发利用卤虫资源,使之成为新的食品源和优质饲料有着广泛的前景．     

5种黄精属植物的蛋白指纹分析

本文用聚丙烯酰胺凝胶电泳（ＳＤＳ—ＰＡＧＥ）技术分析了５种黄精属植物根状茎和叶的蛋白指纹．结果表明：（１）它们的根状茎均含有３８．５、２８、１８．６ｋＤ蛋白质;（２）根状茎和叶的蛋白质种类有很大差异;（３）５种黄精属植物各含有自己特有的蛋白质,它们在本属植物物种鉴定中一定参考价值．     

阳离子反胶团体系提取蛋白质

用阳离子反胶团体系分别对４种蛋白质进行反胶团提取的试验和考察,确定ＰＨ值,离子强度,表面活性剂浓度和助溶剂等影响提取的主要因素。     

超滤法分级和纯化蛋白质的现状和前景(英文)

超滤法具有高产率、低成本、容易放大等显著优点,但其低选择性一直限制其在生物蛋白制品的分级和纯化中的应用。本文总结和分析了超滤法用于蛋白质分级和纯化的近期研究成果,对其低选择性的原因进行了分析,提出并论证了提高超滤选择性的技术途径。     

青海高原春小麦籽粒蛋白质积累规律研究

分析了阿勃,青春５３３,青农４６９、青农４５２等四个春小麦品种（品系）在青海西宁地区籽粒蛋白质相对含量的变化规律和蛋白质绝对含量的积累进程,结果表明,从开花至成熟,籽粒蛋白质相对含量的变化呈“Ｕ”型曲线,并以花后籽粒发育初期含量最花,花后３１天左右是该地区春小麦籽粒中蛋白质相对含量最低的时期。不同品种在花后不同时期蛋白质相对含量各不相同;籽粒蛋白质绝对含量的积累过程呈“Ｓ”形曲线,可用概率转换方程     

Molecular evidence for increased hematopoietic proliferation in the spleen of the b/b laboratory rat

The splenomegaly and the appearance of a significant number of CFU-E (erythroid colony-forming units) and BFU-E¹ (erythroid burst-forming units) in the Belgrade laboratory rat (b/b) spleen prompted us to analyse further the molecular evidence for increased hematopoietic proliferation in the b/b spleen. Messenger RNAs (mRNAs) specific for globins, proteins for iron transport and deposition and the band 3 protein were used in rat erythropoietic tissues as markers for proliferation and erythroid differentiation. In the b/b spleen, all mRNAs analysed display an erythroid-specific pattern of expression. This analysis also revealed an enhanced level of mRNA for ferritin in the +/b spleen, whereas erythrocyte-specific mRNA production was normal.     

Studies of a key protein in the mechanism of the excitation-contraction coupling process of frog skeletal muscle,using phenylglyoxal

The excitation-contraction (E-C) coupling process in single twitch fibres from frog toe muscle was inhibited selectively by phenylglyoxal (PGO), a specific guanidyl modifying reagent. A new protein (31.5 kDa), which has PGO-binding ability and seems to play a key role in the E-C coupling process, was solubilized from transverse tubule membrane-junctional sarcoplasmic reticulum complexes (TTM-JSR) of frog skeletal muscles, using¹⁴C-PGO. The monoclonal antibody against this protein applied extracellularly inhibited the E-C coupling process of the single fibres. This protein appears to constitute the very first step of input for E-C coupling. It is considered to behave as an indispensable part of an electrometer to measure membrane potentials. Therefore, the name electrometrin is suggested for the new protein.     

Triphasic vascular effects of thiol compounds and their oxidized forms on dog coronary arteries

The vascular effects of 2-mercaptoethanol, cysteamine, L-cysteine, glutathione (GSH), cystamine and oxidized GSH (GSSG) on the isometric tension of isolated dog coronary arterial strips were examined, and these effects were compared with the triphasic response induced by dithiothreitol (DTT); a rapid and weak contraction (phase A), an intervening slow relaxation (phase B) and a slowly-developing strong contraction (phase C) which we previously reported. The responses of the arteries induced by 2-mercaptoethanol, cysteamine and L-cysteine consisted of phases A, B and C. The order of contractile potency (ED₅₀ of phase C) was DTTL-cysteine>2-mercaptoethanolcysteamine, while the order of relaxant potency (ED₅₀ of phase B) was DTT>cysteamine2-mercaptoethanol. GSSG and cystamine mainly produced relaxation, which corresponded to phase B. The phase C contraction was specific to the reduced forms of thiols, except for GSH, which produced only relaxation. The participation of endothelial cells was not essential for the contracting or relaxing effects of the thiol compounds. The phase C contraction was depressed by W-7, a calmodulin antagonist, while phase A was not. Therefore calmodulin-dependent protein kinases may participate in phase C, not in phase A.