秸秆氨化后生物技术处理的工艺

以最佳条件氨化处理后的玉米秸秆为原料,通过对菌种的诱变筛选、固体培养基的组合实验及发酵工艺条件优化等,确定质量分数为70%氨化秸秆末、20%的麸皮与15%的鲜酒糟配料比,采用黑曲霉(经处理)与面包酵母菌种比质量分数为1∶1,经32℃、28h通气发酵,可使蛋白质含量大幅度提高,并获得较满意的植酸酶、酸性蛋白酶、淀粉糖化酶酶活,具有推广应用价值.     

玉米乳酸饮料的研制

利用玉米生产乳酸饮料工艺为,先将玉米用质量分数0.2%的乳酸在50 ℃的水中浸泡48 h,然后用质量分数0.5%的α-淀粉酶液化、0.6%的糖化酶糖化.将糖化液与鲜牛奶以体积分数14∶6的比例混合进行乳酸发酵,可制出优质保健玉米乳酸饮料.     

耐酸性运动发酵单胞菌的筛选和酒精发酵条件的优化

通过酸性平板筛选,在作者所在实验室保藏的运动发酵单胞菌中,得到一株能在pH4.5时进行酒精发酵的菌株,其酒精产量为66.7g/L,与原菌株在pH6.5时的相同.通过单因素实验和正交实验,对该菌在酸性条件下的酒精发酵条件进行了优化.结果表明,在发酵温度为30～35℃,pH4.5,初糖质量浓度150g/L,酵母膏质量浓度4g/L,蛋白胨质量浓度为2g/L时,该菌的酒精产量达到最大,为71.7g/L.     

玉米原料细菌酒精发酵的研究

对运动发酵单胞菌ＺｙｍｏｍｏｎａｓｍｏｂｉｌｉｓＡＴＣＣ３１８２１的试验表明：该菌株最适发酵糖浓度为１５０～２００ｇ／Ｌ，ｐＨ为７左右。以玉米粉为原料，该菌株在发酵速率及淀粉出酒率等方面均比Ｋ字酵母优越。玉米粉在糖化３０ｍｉｎ，添加ＣＡＸ２０ｇ／Ｌ３５℃发酵４０ｈ后，酒精度达７２ｇ／Ｌ残糖（还原糖）４．２ｇ／Ｌ淀粉利用率９１．５％；淀粉出酒率４８．５％（按无水酒精计）。     

HPLC法测定玉米浓醪发酵酒精醪液中的纤维二糖和蜜二糖

采用高效液相色谱分析方法分析浓醪发酵酒精醪液中的纤维二糖和蜜二糖．在分析过程中，对氨基分析柱和碳水化合物分析柱的分离效果、回收率等进行了比较，结果得出碳水化合物分析柱的分析效果比较好，从而初步建立了定性定量分析浓醪发酵酒精糟液中纤维二糖和蜜二糖的方法．     

活性乳酸菌乳饮料高活菌数发酵工艺的优化

探索了获取高活菌数的发酵乳饮料的发酵条件.以温度、营养、接种量为试验因素,通过单因素试验和正交试验方法,考察以上3因素在乳酸菌乳饮料发酵过程中对试验指标乳酸菌数影响的显著性.结果表明,发酵温度对试验结果影响极显著(P<0.01),营养浓度影响显著(P<0.05),接种量影响不显著(P>0.05).进一步的正交试验结果表明,高活菌数的乳饮料的最优化发酵工艺组合为发酵温度29 ℃,奶粉加入量(营养浓度)10 g/dL,接种体积分数5%.     

新鲜木薯直接转化生产乙醇

介绍了利用新鲜木薯生产乙醇的新工艺:用真菌α淀粉酶和降粘酶预处理新鲜木薯醪液,后加入颗粒淀粉水解酶STARGENTM进行酵母酒精发酵.该工艺可直接利用新鲜木薯进行酒精发酵;相比传统高温工艺,该发酵新工艺过程中新鲜木薯醪液粘度显著降低,有更多可发酵性糖被利用,并且最终发酵效率显著提高.     

菊芋原料同步糖化发酵生产丁二酸

对菊芋原料发酵生产丁二酸进行了研究,用 Actinobacillus succinogenes 和 Aspergillus niger 同步糖化发酵,发现同步糖化发酵效果优于糖化后再发酵,在同步糖化发酵过程中还原糖质量浓度始终保持在10～40 g/L,可以避免高浓度的还原糖对 A.succinogenes 的抑制.5 L搅拌罐中同步糖化补料分批发酵96 h产丁二酸98.2 g/L,对消耗糖产率95.4%,生产强度1.02 g/(L·h) .     

纳豆芽孢杆菌的固态发酵条件

为了优化纳豆芽孢杆菌固态发酵条件,以活菌数和芽孢数为指标,采用微生物发酵技术,研究了种龄、接种量、培养基初始pH值和含水量对固态发酵的影响,并通过L9(34)正交试验确定了纳豆芽孢杆菌固态发酵最佳条件.试验结果表明:接种体积分数7%、种龄17 h、培养基初始pH值8.0、培养基初始水分质量分数70%,37℃固态发酵5 d效果最好,活菌数和芽孢数分别达到3.4×1010 cfu/g和1.8×109 cfu/g.     

大米生料发酵酒精生产的研究

报告了新型颗粒淀粉水解酶在大米酒精生产上的最新进展.采用杰能科公司的颗粒淀粉水解酶STARGENTM以大米为原料,发酵效率可大大提高,同时对发酵醪液进行了GC-MS分析结果表明,生料工艺的发酵产物杂质与传统工艺相比也有很大程度上的减少.     

Burdened by training not by anaesthesia

Editor—Larsson and colleagues¹ have investigated importantbut often ignored aspects of anaesthetic practice. However,they imply that specialist anaesthetists experience reducedlevels of stress when compared with trainees because they havedeveloped successful coping mechanisms over the years. Thisconclusion cannot be drawn because the specialists' attitudesto work were identified at a particular time and cannot showa progression in learned coping abilities. To demonstrate thedevelopment of these skills, the specialists would have hadto be interviewed     

Bladder carcinoma treated by preoperative radiotherapy followed by cystectomy

Summary In 1969 a clinical trial was started where patients with bladder carcinoma stage T2 and grade 3 were subjected to preoperative radiotherapy followed by cystectomy. The survival rate in this series was higher than in a previous series of comparable patients who were given full irradiation without cystectomy.     

Treatment of hemospermia caused by dilated seminal vesicles by direct drug injection guided by ultrasonography

Bilateral seminal vesicle puncture and injection of drugs with ultrasound guidance were performed in patients with hemospermia resistant to conservative therapy and with dilated seminal vesicles. Of 7 patients 6 had resolution of hemospermia for 2 to 3 months and then relapse. No side effect was noted.     

Amplification by hyperoxia of coronary vasodilation induced by propofol

We tested the hypothesis that in vitro coronary and myocardial effects of propofol (10-300 microM) should be significantly modified in an isolated and erythrocyte-perfused rabbit heart model in the absence (PaO(2) = 137 +/- 16 mm Hg, n = 12) or in the presence (PaO(2) = 541 +/- 138 mm Hg, n = 12) of hyperoxia. The induction of hyperoxia provoked a significant coronary vasoconstriction (-13% +/- 7%). Propofol induced increased coronary vasodilation in the presence of hyperoxia. Because high oxygen tension has been reported to induce a coronary vasoconstriction mediated by the closure of adenosine triphosphate-sensitive potassium channels, we studied the effects of propofol in 2 additional groups of hearts (n = 6 in each group) pretreated by glibenclamide (0.6 microM) and cromakalim (0.5 microM) in the absence and presence of hyperoxia, respectively. The pretreatment by glibenclamide induced a coronary vasoconstriction (-16% +/- 7%) which did not affect propofol coronary vasodilation. The pretreatment by cromakalim abolished the amplification of propofol coronary vasodilation in the presence of hyperoxia. Propofol induced a significant decrease in myocardial performance for a concentration >100 micro M both in the absence and presence of hyperoxia. We conclude that propofol coronary vasodilation is amplified in the presence of hyperoxia. This phenomenon is not explained by the previous coronary vasoconstriction induced by glibenclamide. However, the pretreatment of hearts by cromakalim abolished the amplification of propofol coronary vasodilation in the presence of hyperoxia. The myocardial effects of propofol were not affected by the presence of hyperoxia. IMPLICATIONS: Propofol induced a coronary vasodilation that was amplified in the presence of hyperoxia. This phenomenon does not seem to be related to previous coronary vasoconstriction. The myocardial effects of propofol were not significantly modified in the presence of hyperoxia.     

Direct plexus repair by grafts supplemented by nerve transfers

This article reviews the Louisiana State University Health Sciences Center experience with direct repair of brachial plexus lacerations, gunshot wounds, and stretch/contusive/avulsive injuries. In the stretch category, limited outcomes with direct repair have led to addition of nerve transfers rather than their exclusive use. It is important to per-form direct plexus repair in conjunction with nerve transfers in the same patient when-ever possible. The intent of such a "pants-over-vest" approach is to maximize axonal input to denervated structures.     

Lavage by laparoscopy fares better than lavage by laparotomy

Background: Although carbon dioxide (CO2) pneumoperitoneum is proposed increasingly for treatment of secondary peritonitis, associated deleterious effects have been reported in experimental models, with the hypothesis that increased intraperitoneal pressure might facilitate bacterial translocation. The purpose of this study was to compare the outcome (and qualitative microbiologic analysis) from peritonitis in rats after lavage by laparoscopy with the outcome after lavage by laparotomy. Methods: After determination of the standard innoculum for this study in 30 animals, 120 male Wistar rats received 1 ml of Escherichi coli 106 colony-forming unit (CFU), Bacteroides fragilis 107 CFU, Enterococcus faecalis 107 CFU in a sterile rat feces-barium sulfate suspension adjuvant, were anesthetized with intramuscular ketamine, and then underwent peritoneal lavage by either laparotomy (n = 60) or laparoscopy (n = 60). The duration of peritonitis defined two groups: group A: duration less than 3 h (n = 20) and group B: duration 3 h or more (n = 40). Both groups underwent successive lavage with 10-ml aliquots (total, 50 ml) of 0.9% saline solution at 37°C. Five 2-ml samples of liquid lavage were drawn for culture and microbiologic analysis. Blood (0.2 ml) and peritoneal liquid lavage samples were incubated 48 h at 37°C and cultured. Results: All the animals survived. Mean duration of peritoneal lavage was 13.2 min (range, 6-25 min) for laparoscopy and 9.7 min (range, 6-15 min) and for laparotomy. The difference was not statistically significant. The mean duration of operation was significantly longer with laparoscopy than with laparotomy: 44.5 min (range, 35-62 min) and 25 min (range, 16-40 min), respectively (p = 0.0001). The collected lavage volumes were not statistically different: 48.5 ml (range, 40-54 ml) and 46.7 ml (range, 37-56 ml), respectively. No statistically significant differences were found between the laparoscopy and laparotomy groups in terms of E. coli bacteremia, irrespective of peritonitis duration. The rates of positive blood culture for B. fragilis and E. faecalis were signficantly lower after laparoscopy than after laparotomy, both in the overall group (p = 0.025 and p = 0.045, respectively) and when duration of peritonitis exceeded 3 h (p = 0.001 and p = 0.044, respectively). Conclusions: In this animal model of secondary peritonitis, lavage by laparoscopy was associated with less bacteremia for B. fragilis and E. faecalis than peritoneal lavage by laparotomy.