Determinants of growth-promoting activity reside in the A-domain of insulin-like growth factor I

A two-chain, disulfide linked, insulin-like compound embodying the A-domain of insulin-like growth factor I (IGF-I) and the B-chain of insulin has been synthesized and characterized with respect to insulin-like biological activity and growth-promoting potency. The compound displays a potency of ca. 41% relative to insulin in assays for insulin-like activity (e.g., lipogenesis) but significantly higher activity than insulin, ca. 730% relative to insulin, in growth factor assays (e.g., thymidine incorporation). The compound is, however, a less potent growth factor than IGF-I itself, ca. 26.5% relative to IGF-I, and is not recognized by IGF carrier proteins. We conclude that structural features contained in the A-domain of IGF-I are primarily responsible for the growth-promoting ability displayed by IGF-I, while features in the B-domain are responsible for recognition by IGF carrier proteins.     

四川盐源盆地哺乳类化石及其意义

本文简述盐源盆地上新世和更新世晚期两个不同时代的哺乳动物化石十余种,据之修正了该盆地晚新生代沉积的时代和对比关系.     

Mechanism of activation of 1,2-dehydro-N-acetyldopamine for cuticular sclerotization

The mechanism of oxidation of 1,2-dehydro-N-acetyldopamine (dehydro NADA) was examined to resolve the controversy between our group and Andersen's group regarding the reactive species involved in β-sclerotization. While Andersen has indicated that dehydro NADA quinone is the β-sclerotizing agent [Andersen, 1989], we have proposed quinone methides as the reactive species for this process [Sugumaran, 1987; Sugumaran, 1988]. Since dehydro NADA quinone has not been isolated or identified till to date, we studied the enzymatic oxidation of dehydro NADA in the presence of quinone traps to characterize this intermediate. Accordingly, both N-acetylcysteine and o-phenylenediamine readily trapped the transiently formed dehydro NADA quinone as quinone adducts. Interestingly, when the enzymatic oxidation was performed in the presence of o-aminophenol or different catechols, adduct formation between the dehydro NADA side chain and the additives had occurred. The structure of the adducts is in conformity with the generation and reactions of dehydro NADA quinone methide (or its radical). This, coupled with the fact that 4-hydroxyl or amino-substituted quinones instantly transformed into p-quinonoid structure, indicates that dehydro NADA quinone is only a transient intermediate and that it is the dehydro NADA quinone methide that is the thermodynamically stable product. However, since this compound is chemically more reactive due to the presence of both quinone methide and acylimine structure on it, the two side chain carbon atoms are “activated.” Based on these considerations, it is suggested that the quinone methide derived from dehydro NADA is the reactive species responsible for cross-link formation between dehydro NADA and cuticular components during β-sclerotization.     

中国的脊棱齿象属(Stegolophodon)化石

剑齿象属 Stegodon 起源于脊棱齿象属 Stegolophodon,两者都是亚洲大陆晚新生代的特有动物,本文讨论两属中一些种的性质和分类位置问题,并记述了药铺脊棱齿象 Stegolophodon officinalis 的新材料.     

青龙河底栖无脊椎动物群落结构及其水质评价

本文论述了青龙河底栖生物种类、数量、分布和结构等特点及其与环境因子间的关系。应用Beck、Gleason、Shannon、Simpson等生物指数对水质状况进行评价。结果表明青龙河除个别断面受污染外,大部分河段属尚清洁水。     

Bioconversion of organosilicon compounds by horse liver alcohol dehydrogenase: the role of the silicon atom in enzymatic reactions

Summary Bioconversion of three organosilicon compounds of different chain length between the silicon atom and the hydroxyl group (Me₃Si(CH₂)_nOH, n = 1–3) by horse liver alcohol dehydrogenase (HLADH, EC 1.1.1.1.) was studied. Furthermore, the effect of the silicon atom on the HLADH-catalysed reaction was examined in comparison with the corresponding carbon compounds. HLADH could catalyse the dehydrogenation of trimethylsilyeethanol (n = 2) and trimethylsilylpropanol (n = 3). Trimethylsilylethanol was a better substrate than both its carbon analogue, 3,3-dimethylbutanol, and ethanol. The improved activity of HLADH on trimethylsilylethanol could be accounted for by a higher affinity toward HLADH and a lower activation energy of the reaction by HLADH than those of the carbon counterpart. These are derived from physical properties of the silicon atom, that is, the lower electronegativity and the bigger radius than those of the carbon atom. In contrast, HLADH showed no activity on trimethylsilylmethanol (n = 1), whereas it catalysed the dehydrogenation of the carbon analogue, 2,2-dimethylpropanol, fairly well. The reason for the inactivity of HLADH in the case of trimethylsilylmethanol based on the electric effect of the silicon atom is also discussed. Offsprint requests to: A. Tanaka     

阿坝藏族自治州若尔盖晚更新世地层及哺乳类化石

文中记述阿坝藏族自治州若尔盖县境内黄河阶地堆积及其所产哺乳动物化石,并经 C~(14) 测定,化石距今约22650±300年,地质时代为晚更新世晚期.     

我国特有植物银杉的资源、分布及其环境

我国银杉自1955年发现以来,陆续发现了它的新分布,至今已知在四省、区7个分布区的30多个分布点上,自然生长着银杉3200余株。它们是:广西花坪林区(越城岭南部)6个点有银杉1040抹,其中高5米以上的68株,1～5米的49株,1米以下的923株,最高21.1米,最大胸径83厘米;广西大瑶山4个点有银杉143株,其中高10米以上的94株,1～3米的3株,1米以下的46株,最高30米,最大胸径79.2厘米;湖南罗汉洞(越城岭北部)2个点有银杉58株,5米以上的有45株,最高18米,最大胸径43厘米;湖南罗霄山脉八面山有银杉707株,高1米以上的334株,最高24米,最大胸径46厘米;四川南川金佛山(大娄山东段北部)6个点有银杉527株,其中成年树400余株,最高17米,最大胸径50厘米;百枝山有银杉52株,最高8米,最大胸径27厘米;贵州道真沙河林区(大娄山东段南部)3处12个点有银杉729株,其中高5米以上的105株,2～5米的209株,1～2米的111株,1米以下的304株,最高18.8米,最大胸径48厘米;贵州桐梓白菁有银杉10株,高4～5米的2株,1～3米的6株,1米以下的2株。 银杉分布区范围自北纬24°5′～29°13′14″,东经107°10′～113°40′。其垂直分布自海拔940～1840米,金佛山银杉分布最高,为1600～1840米;罗汉洞银杉分布最低,为940～1060米。分布区内,年均温8.2°～17℃,绝对最低温