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排序方式: 共有825条查询结果,搜索用时 437 毫秒
1.
从上海光明乳业股份有限公司车间发酵罐中分离出4株酸奶噬菌体。1号噬菌体头部呈六角形,平均直径为95.1nm,头部剖面平均面积为8184.8nm^2,尾部的平均直径为18.3nm,平均长度为403.4nm;2号噬菌体头部呈六角形,平均直径为85.4nm,头部剖面平均面积为8046.2nm^2,尾部的平均直径为23.3nm,平均长度为549.4nm;3号噬菌体头部呈六角形,平均直径为95.5nm,头部剖面平均面积为9792.3nm^2,尾部的平均直径为19.8nm,平均长度为450.5nm;4号噬菌体头部呈六角形,平均直径为119.3nm.头部剖面平均面积为12586.1nm^2,尾部的平均直径为23.6nm,平均长度为520.5nm。 相似文献
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Melissa trogdon Hines DVM PhD Jerry R. Heidel DVM PhD David D. Barbee DVM MS 《Veterinary radiology & ultrasound》1993,34(1):47-51
A 2.5 year old Appaloosa stallion with progressive weight loss and a heart murmur was diagnosed as having vegetative endocarditis of the right atrioventricular valves with a mass in the right atrium. The ultrasonographic appearance of the lesion was characterized by extreme reverberation. On postmortem examination, a 9 cm diameter thrombus was found within the right atrium and auricle, occupying approximately 80% of the chamber volume. Additionally, a lenticular abscess extended throughout the parietal cusp of the right atrioventricular valve. Histologic examination revealed that the lesions were septic with numerous gram positive cocci in short chains, suggestive of Streptococcus equi , and gram negative rods. 相似文献
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The changes of redox potential were measured in growing cultures of three strains of Streptococcus bovis, together with three strains of Staphylococcus aureus and one strain of each of Lactobacillus plantaram, Lactobacillus casei, and Eschericia coli. It was found that both S. aureus and E. coli could reduce the redox potential of the growth medium to very low values (between —400 mv and —600 mv), whereas the streptococci and lactobacilli were able to cause only slight or insignificant changes of the redox potential. Respirometric measurements confirmed that the capacity of oxygen consumption of S. bovis was very small compared to that of E. coli and S. aureus. On this basis the authors conclude that S. bovis in all probability is unable to contribute significantly to maintenance of the low redox potential of its natural habitat, the rumen. This function must be carried out by other bacteria, such as enterobacteria or staphylococci, which are capable of performing a true, aerobic respiration. 相似文献
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Grass fructans can be fermented by Gram-positive bacteria (e.g., Streptococcus bovis) in the equine hindgut, increasing production of lactic acid and decreasing pH. The degree of polymerization (DP) of fructans has been suggested to influence fermentation rates. The objective of the present study was to determine how DP impacts fermentation by equine fecal bacteria and a model S. bovis. Fecal microbes from three mares were harvested by differential centrifugation, washed, and resuspended in anaerobic media containing short-chain (SC; DP ≤ 10) or long-chain (LC) inulin (DP ≥ 23) from 0% to 2% wt/vol. After 24 hours of incubation (37°C), samples were collected for pH determination. Data were analyzed using the general linear models (GLM) procedure testing for the effect of treatment, concentration, and treatment × concentration (SAS v. 9.3). At all concentrations, the pH was lower in SC fermentations than in LC (P < .0001, in all cases). To determine the effect of DP on S. bovis, cultures were grown (39°C, 9 hours) with 0.1%, 0.5%, or 1.3% SC or LC inulin. Optical density (600 nm) was determined by spectrophotometry. Maximum specific growth rates (μ) were determined by linear regression (2–5 hours). Data were analyzed using the one-way analysis of variance procedure (SAS v. 9.3). The final optical density (600 nm), μ, and yield were higher with SC than with LC fermentation (P < .05). These results indicate that SC inulin may be more available for fermentation than LC inulin by equine fecal bacteria and S. bovis, specifically. 相似文献
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为构建猪链球菌(Streptococcus suis)蛋白表面展示系统,本研究通过序列分析,确定猪链球菌的LPxTG蛋白及其信号肽(SP)和胞壁锚定基序(CWA),通过PCR扩增Peno-SP、GFP、CWA的DNA片段并融合,构建强启动子Peno控制表达编码SP-GFP-CWA融合蛋白的DNA片段,将该重组DNA片段连接pSET2载体,获得蛋白表面展示质粒,转化猪链球菌,构建得到以GFP为报告蛋白的猪链球菌蛋白表面展示系统。结果显示,利用猪链球菌的10个LPxTG蛋白及其SP和CWA序列,构建了10个含有Peno-SP-GFP-CWA融合片段的重组pSET2表面蛋白展示质粒pSsPSD1至pSsPSD10,分别转化猪链球菌05ZYH33,PCR鉴定显示其中7个转化猪链球菌。采用western blot初步检测其展示蛋白,结果显示,7个转化阳性菌株均能有效表达GFP蛋白,以成熟GFP条带为指标,均表现出了一定的外源GFP表面展示水平,分别命名为SsPSD1、SsPSD2、SsPSD4、SsPSD7-SsPSD10,其中SsPSD1、SsPSD4、SsPSD8和SsPSD9表面展示水平相对较好,在猪链球菌表面展示外源蛋白方面具有很好的潜力。本研究首次尝试建立猪链球菌蛋白表面展示系统,为猪链球菌表面递呈外源蛋白或抗原提供了新的策略。 相似文献
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