Growth rates of Tilapia esculenta (Graham) and Tilapia zillii (Gervais) under cultivation in ponds at Nyegezi, Tanzania

Aquaculture in Tanzania is still on a subsistence level and most of the ponds are maintained as part time job. The ponds are too small, shallow and over crowded with stunted Tilapia spp. In the present paper the results of experiments conducted in ponds at Nyegezi with T. esculenta and T. zillii are presented. This was part of an overall project of developing techniques of fish cultures with Tilapia under the limited existing conditions at Nyegezi. In a mono - species culture experiement with Tilapia zillii in nine month's time an average size of 172.8 mm/115.0 g was attained. In another experiment with T. zillii and T. esculenta in thirteen month's time, T. zillii attained an average size of 180.2mm/106.6 g and T. esculenta 193.6 mm/118.8 g. In another experiment with intensive feeding schedule an average size of 179.3 mm/126.6 g was attained by T. zillii and 191.0 mm/125.0 g by T. esculenta in four month's time. A locally prepared supplimentary feed with local Brewery Waste and Fish Meal (10:1) was readily accepted by both species of Tilapia. T. zillii voraciously fed on Cabbage leaves, Cauliflower leaves, Chinese cabbage leaves, Cassava leaves and on the common weed Comalina sp. Though all the items mentioned above were readily accepted by T. zillii feeding with Comaltna sp. was the easiest and most convenient because of its availability. In an intensive feeding experiment with vegetable leaves/Comalina sp. and the locally prepared supplimentary feed the fishes attained table size in four months time. Cement cistens of 5 X 3 X 1½ m size could be conveniently used for breeding both species of Tilapia. T. zillii had semi adhesive eggs and they were deposited on the sides of the cement wall. The number of young ones in a brood ranged from 160 to 314 in T. esculenta and 687 to 4,356 in T. zillii.

树鼩CXCR4cDNA的克隆和序列分析

　目的　获得树　CXCR4 的cDNA 序列,探讨其是否可以支持HIV-1 病毒和细胞的结合。方法　设计 相应的引物, 用RT- PCR ,基因克隆,DNA 序列分析技术。结果　获得了全长为1059bp 树　CXCR4 (tsCXCR4) 基因 的cDNA。发现其核苷酸序列与人的CXCR4 (hCXCR4) 基因的cDNA 有9218 % 的相似性,由此推导出的氨基酸序列 有9619 % 相似性。与hCXCR4 功能相关的关键位点完全相同,tsCXCR4 的N 端第7 和12 位点为酪氨酸,第14、15 和 32 位点为谷氨酸,胞外环第183 ,188 为精氨酸, 第193、262 位点以及跨膜区97 位点为天冬氨酸。结论　树　的CX2 CR4 很可能会作为HIV-1 的辅助受体。　

猕猴输精管内注射高分子聚合物HFMC后对睾丸组织结构的影响

本实验选用具有生育力成年雄性猕猴７只，在直视下行双侧ＨＦＭＣ输精管内注射，每侧剂量分别为３０ｍｇ１只，６０ｍｇ和１００ｍｇ各３只；于注射后２．５年和３．５年分别处死动物，取睾丸组织进行光镜和电镜观察．结果发现：猕猴注射ＨＦＭＣ２．５年后，睾丸光镜大部分曲细精管生精上皮结构完整，排列整齐。仅见局部少数管腔生精上皮层数减少，上皮细胞轻度水样变性等病理改变。电镜下曲细精管内除支持细胞内脂褐素增多，轻度基底膜增厚和精母细胞内质网扩张外，各级生精细胞，支持细胞及细胞间连接复合体等超微结构未见明显异常。注射ＨＦＭＣ３．５年后猕猴的光镜、电镜结果与注射后２．５年结果相似，但局部改变较２．５年组轻。上述结果表明：猕猴输精管内注射一定剂量ＨＦＭＣ节育不会引起睾丸组织的严重病理改变。但是，由于注射ＨＦＭＣ后，ＨＦＭＣ释放Ｈ＋及其对输精管的暂时阻塞，改变了精子生存的内环境，使睾丸出现局部轻度病理改变，随着ＨＦＭＣ逐渐溶解排出，睾丸功能相继恢复正常，配对产仔。为ＨＦＭＣ应用提供了安全性依据。

翻译速率与蛋白质二级结构的关系

统计分析了人的119种蛋白质和大肠杆菌的92种蛋白质密码子翻译速率和蛋白质二级结构的关系。据 二密码子片段在不同二级结构中的频数分布，我们发现人和大肠杆菌中翻译速率与蛋白质二级结构之间有一定 关系:高翻译速率时倾向编码。螺旋、不倾向编码线团(coil);低翻译速率时倾向编码线团、不倾向编码。螺旋;R 折叠结构则随翻译速率表现出明显的振荡。同时，密码子的使用在不同片段内一般也是不均匀的:在。螺旋片段 内，结构尾部偏向使用高翻译速率密码子;中部倾向使用中翻译速率密码子;而头部使用的密码子翻译速率偏 低。这样的倾向性不大可能归结为随机起伏的影响。

The relation between translation speed and protein secondary structure

Based on the statistical analysis of 119 human and 92 E. coli proteins it was found that for both human and E. coli, the mRNA sequences consisting of tri-codon and tetra-codon with high translation speed preferably code for alpha helices more than for coils. For beta strand, the preference/ avoidance oscillates with the translation speed. Moreover, the non-homogeneous usages of tri-codon and tetra-codon with different translation speeds in a given secondary structure have also been found. These results cannot be simply explained by the effect of stochastic fluctuation.