树鼩(Tupaia belangeri chinensis)生长发育的初步观察

本文对39只树鼩的个体生长发育作了描述。新生幼仔生长发育迅速,在出生后头一个月内,体重可增长3—6倍,其体重的增长与饮奶量有关。出生后4个月性成熟,7个月龄时可繁殖产仔。性器官的重量有明显的季节性变化,1—6月间睾丸、子宫、卵巢重量最大,性行为活跃,其余月份重量下降,性功能出现渐进性衰退。辜丸重和体重的比值小于0.01,表明树鼩是单雄交配繁殖。乳齿的萌发为下颚先于上颚,门齿最先萌发,其次是犬齿,前臼齿,最后是臼齿。与Lyon(1913)和Shigehara(1980)提出的恒齿萌发次序不同。     

恒河猴日需蛋白质量的研究

本文报道了恒河猴(Macaca mulatta)日需蛋白质量的实验研宄。四组未成年恒河猴(共36只)分别饲喂蛋白质含量为15％、20％、24％的配合饲料和玉米加蚕豆,为时90天。四组动物的平均增重依次为0.3、0.6、0.6和0.2公斤。猴子日食蛋白质含量力20％的饲料,氮在体内的平均沉积率是57±13.5％。实验期间,各组动物血红蛋白,血清总蛋白和血总脂的含量无显著变化。以上结果和在本所试用的饲养效果表明,在我们的饲养条件下,配合饲料中蛋白质含量以20％较有利于恒河猴的生长发育和节约费用。     

Malonyl-CoA: acyl carrier protein transacylase from Helicobacter pylori: Crystal structure and its interaction with acyl carrier protein

Malonyl-CoA: acyl carrier protein transacylase (MCAT) is a critical enzyme responsible for the transfer of the malonyl moiety to holo-acyl carrier protein (ACP) forming the malonyl-ACP intermediates in the initiation step of type II fatty acid synthesis (FAS II) in bacteria. MCAT has been considered as an attractive drug target in the discovery of antibacterial agents. In this study, the crystal structure of MCAT from Helicobacter pylori (Hp) at 2.5 angstroms resolution is reported, and the interaction of HpMCAT with HpACP is extensively investigated by using computational docking, GST-pull-down, and surface plasmon resonance (SPR) technology-based assays. The crystal structure results reveal that HpMCAT has a compact folding composed of a large subdomain with a similar core as in alpha/beta hydrolases, and a similar ferredoxin-like small subdomain as in acylphosphatases. The docking result suggests two positively charged areas near the entrance of the active site of HpMCAT as the ACP-binding region. Binding assay research shows that HpMCAT demonstrates a moderately binding ability against HpACP. The solved 3D structure of HpMCAT is expected to supply useful information for the structure-based discovery of novel inhibitors against MCAT, and the quantitative study of HpMCAT interaction with HpACP is hoped to give helpful hints in the understanding of the detailed catalytic mechanisms for HpMCAT.     

Helicobacter pylori acyl carrier protein: expression, purification, and its interaction with beta-hydroxyacyl-ACP dehydratase

Acyl carrier protein (ACP) is an essential component in the type II fatty acid biosynthesis (FAS II) process and is responsible for the acyl group transfer within a series of related enzymes. In this work, the ACP from Helicobacter pylori strain SS1 was cloned and the gene sequence of Hpacp was deposited in the GenBank database (Accession No.: AY904356). Two forms of HpACP (apo, holo) were successfully purified and characterized. The thermal stability of these two forms was quantitatively investigated by CD spectral analyses. The results revealed that the holo-HpACP was more stable than apo-HpACP according to the transition midpoint temperature(Tm). Moreover, the interaction of HpACP with the related enzyme (beta-hydroxyacyl-ACP dehydratase, HpFabZ) was determined by GST-pull down assay and surface plasmon resonance (SPR) technique in vitro, the results showed that HpACP displays a strong binding affinity to HpFabZ (KD=1.2 x 10(-8)M). This current work is hoped to supply useful information for better understanding the ACP features of Helicobacter pylori SS1 strain.     

Establishment of customized mouse stem cell lines by sequential nuclear transfer

Therapeutic cloning, whereby embryonic stem cells （ESCs） are derived from nuclear transfer （NT） embryos, may play a major role in the new era of regenerative medicine. In this study we established forty nuclear transfer-ESC （NTESC） lines that were derived from NT embryos of different donor cell types or passages. We found that NT-ESCs were capable of forming embryoid bodies. In addition, NT-ESCs expressed pluripotency stem cell markers in vitro and could differentiate into embryonic tissues in vivo. NT embryos from early passage RI donor cells were able to form full term developed pups, whereas those from late passage RI ES donor cells lost the potential for reprogramming that is essential for live birth. We subsequently established sequential NT-RI-ESC lines that were developed from NT blastocyst of late passage R 1 ESC donors. However, these NT-R I-ESC lines, when used as nuclear transfer donors at their early passages, failed to result in live pups. This indicates that the therapeutic cloning process using sequential NT-ESCs may not rescue the developmental deficiencies that resided in previous donor generations.     

Quantitative investigation of vascular response to mesenteric venous thrombosis using large‐field‐of‐view photoacoustic microscopy

Mesenteric venous thrombosis (MVT) is one of major causes leading to severe mesenteric ischemia. Vascular network plays an important role during the occurrence and development of MVT. However, there lacks an appropriate imaging method, which features advanced volumetric resolving capability, superior sensitivity to hemoglobin, and ultra‐large field‐of‐view (FOV), to investigate vascular response of MVT. In this study, we developed and applied a large‐FOV optical resolution photoacoustic microscopy to quantify the vascular response during the entire course of two different MVT models in which we ligated the superior mesenteric vein and inferior mesenteric vein, respectively. Furthermore, we developed a quantitative algorithm to derive total vascular length, relative concentration of total hemoglobin and vascular density over the FOV to reveal different vascular responses in different MVT models.     

电刺激采集大额牛精液及其超低温冷冻的初步研究

大额牛 (Ｂｏｓｆｒｏｎｔａｌｉｓ)又名独龙牛 ,俗称野牛 ,是一种半野生半家养 ,为数不多的珍稀濒危牛种 ,仅分布于云南怒江州的独龙江一带。它有着典型的肉用体型 ,耐粗饲 ,抗逆性强 ,肉质细腻 ,是一种有待于进一步开发和极有应用前景的珍稀品种[1] ,由于大额牛的发现比较晚[2 ] ,除了对大额牛的细胞核型、起源和进化、遗传多样性、肉质特性的研究外[3～ 6 ] ,目前 ,对大额牛缺少更多的研究。本文首次对大额牛进行电刺激采集精液和大额牛精液超低温冷冻方法研究 ,为保护和利用大额牛这一濒危物种资源提供一种技术方法。1　材料和方法1 1…     

The successful double cryopreservation of rabbit (Oryctolagus cuniculus) semen in large volume using the directional freezing technique with reduced concentration of cryoprotectant

Using directional freezing, our objective was to cryopreserve rabbit semen and achieve fertility that was equal or higher than that achieved with conventional freezing. The working hypothesis was that controlling the ice-front propagation would allow reduction of DMSO concentration to <1M, in addition to the capability to freeze large volumes (2-10 mL). Moreover, single and double freezing of semen were used to demonstrate the abbreviated mechanical stress imparted by directional freezing. Single-cryopreserved semen from 15 males extended with 0% egg yolk/1.75 M DMSO, 15.3% egg yolk/0.88 M DMSO and 20% egg yolk/0M DMSO resulted in lower (P<0.05) mean+/-S.E.M. post-thaw motility (3.6+/-1.1, 28.5+/-2.8 and 36.3+/-1.8%, respectively) compared to fresh semen (73.3+/-1.2%). Semen from seven of these males, subject to double freezing using only egg yolk based extenders, resulted in post-thaw motilities of 18.1+/-2.2 and 16.4+/-3.3%. Despite the reduced functional parameters of cryopreserved semen, fertility and kindling rates of 73.9 and 56.5% for single frozen-thawed, and 28.6 and 35.7% for double frozen-thawed semen were achieved (with insemination of 98 females). There was no significant difference in fertility rate between fresh semen (87.5%) and semen that was single frozen-thawed with the 15.3% egg yolk/0.88 M DMSO extender (73.9%). In conclusion, cryopreservation of rabbit semen in large volumes using directional freezing achieved fertility rates similar to those achieved with fresh semen. Furthermore, acceptable fertility rates with double frozen-thawed semen could facilitate the future use of sex-sorted semen in rabbits.