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| 1 | TLC及HPLC测定红曲产品中的桔霉素显示文摘阐述了定性及定量测定红曲产品中桔霉素含量的几种方法 .采用板层析 (TLC) ,在点样量为 1mL、点样长度 5cm条件下通过目视法 ,标准桔霉素溶液的最低检测质量浓度可达 0 .2mg/L ,板层析可作为定性检验红曲产品中桔霉素的简便方法 .根据红曲样品预处理方法及HPLC检测器的不同 ,确定了两套准确可靠的定量检测方法 .高效液相色谱结合荧光检测的最低检测限为 0 .60ng .HPLC上样液最低可检测的质量浓度为 0 .1mg/L .在 0 .1~ 1 0mg/L的质量浓度范围内 ,标准桔霉素溶液的质量浓度与峰面积的线性关系良好 ,达到R2 =0 .998. | 陈蕴 许赣荣 顾玉梅 Philippe BLANC | 2001 | 无锡轻工大学学报(食品与生物技术)2001,20,2: | 38 |
| 2 | 无桔霉素红曲色素突变株FM5183对单谷氨酸钠(MSG)、组氨酸的代谢特性显示文摘经过复合诱变处理得到的产无桔霉素的红曲色素变异株 ,编号为FM51 83,在摇瓶条件下分批深层培养 ,研究了菌株在碳源为葡萄糖条件下对单谷氨酸钠 (MSG)、组氨酸的代谢特性 ,该菌株分别在含MSG和组氨酸情况下 ,对产生的中间产物苹果酸和乙醇的代谢特性进行了比较 ,结果表明 :突变菌株FM51 83产生的酒精量为 2 5~ 2 7g L ,苹果酸浓度最大值为 5 8g L ;另外 ,在含MSG和组氨酸的培养基上对产生的色素量进行测定 ,其色价分别为 2 5 5和 1 1 8,对试验所用的氮源等条件下 ,整个发酵过程未有桔霉素检出。突变菌株FM51 83是一株较理想的无桔霉素红曲色素工业化生产菌株。 | 吴祖芳 翁佩芳 张礼星 Philippe J BLANC | 2002 | 生物技术2002,12,6: | 6 |
| 3 | 混合培养微生物利用甘油补料发酵生产乙醇研究显示文摘采用浸麻芽孢杆菌和红曲菌9906利用甘油混合发酵生产乙醇.结果表明,分批发酵中高浓度的甘油对乙醇发酵有着较强的抑制作用,分批发酵最佳甘油浓度为0.217molL-1.在分批发酵的基础上补料发酵,考察了不同甘油浓度的补料液和不同补料时间对乙醇发酵的影响.最终确定乙醇补料发酵较优的工艺条件为:反应器1L,装液量700mL红曲发酵液,甘油初始浓度为0.217molL-1,以补料方式每隔60h分5次补加0.217molL-1甘油浓度的红曲发酵液,每次补加100mL,发酵培养360h.当乙醇最高浓度达0.221molL-1,乙醇总产率0.628mmolh-1,乙醇/甘油转化率达87%(molmol-1).与分批发酵相比,补料发酵很大程度解除了高浓度甘油的抑制作用,有效地利用了甘油,提高了乙醇的产量,且乙醇产率较为稳定. | 张宏武 王璐 许赣荣 BLANC Philippe J | 2008 | 应用与环境生物学报2008,14,5: | 6 |
| 4 | Microorganisms and microalgae as sources of pigments for food use: a scientific oddity or an industrial reality?显示文摘 | Laurent Dufossé Patrick Galaup Anina Yaron Shoshana Malis Arad Philippe Blanc Kotamballi N. Chidambara Murthy Gokare A. Ravishankar | 2005 | Trends in Food Science & Technology2005,,: | 1 |
| 5 | Acute hepatitis A in a pregnant woman at delivery显示文摘 | Anne Motte Julie Blanc Philippe Minodier Philippe Colson | 2008 | International Journal of Infectious Diseases2008,,2: | 1 |
| 6 | Treatment of Unexplained Syncope: A Multicenter, Randomized Trial of Cardiac Pacing Guided by Adenosine 5′-Triphosphate Testing显示文摘 | Daniel Flammang Timothy R. Church Luc De Roy Jean-Jacques Blanc Jean Leroy Georges H. Mairesse Akli Otmani Pierre J. Graux Robert Frank Philippe Purnode | 2012 | Circulation2012,,1: | 1 |
| 7 | Characterization of the Tea Fungus Metabolites显示文摘 | Philippe J BLANC | 1996 | Biotechnology Letters1996,18,2: | 1 |
| 8 | Influence of nitrogen and iron limitation on lipid production by crytococcus curvatus grown in batch and fed-batch culture显示文摘 | MainuL Hassan Philippe J Blanc Louis Mar Granger | 1996 | Process Biochemistry1996,31,4: | 1 |
| 9 | Survival of alginate-entrapped cells of Azospirillum lipoferum during dehydration and storage in relation to water properties显示文摘 | Etienne Paul Jacques Fages Philippe Blanc Gerard Goma Alain Pareilleux | 1993 | Applied Microbiology and Biotechnology1993,,1: | 1 |
| 10 | Characterization of the Tea Fungus Metabolites显示文摘 | Philippe J BLANC | 1996 | Biotechnology Letters1996,18,2: | 1 |
| 11 | Ignition study of acetone/air mixtures by using laser-induced spark显示文摘 | Virginie Tihay Philippe Gillard Denis Blanc | 2012 | Journal of Hazardous Materials2012,,: | 1 |
| 12 | Characterization of the tea fungus metabolites显示文摘 | Philippe J Blanc | | 0,,2: | 1 |
| 13 | Kineticanalysis of red pigment and citrinin production by Monascusruberas a function of organic acid accumulation 显示文摘 | Hassan Hajjaj Philippe Blanc Evelyne Groussac | 2000 | Enzyme and Microbial Technology2000,,27: | 1 |
| 14 | Growth kinetics and astaxanthin production of Phaffia rhodozyma on glycerol as a carbon source during batch fermentation显示文摘 | Endang Kusdiyantini Philippe Gaudin Gérard Goma Philippe J. Blanc | 1998 | Biotechnology Letters1998,,10: | 1 |
| 15 | Influence of nitrogen and ironlimitation on lipid production by crytococcus curvatus grown in batch and fed-batch culture显示文摘 | Mainu L Hassan Philippe J Blanc Louis Mar Granger | 1996 | Process Biochem1996,31,4: | 1 |
| 16 | Characterization of the Tea Fungus Metabolites显示文摘 | Philippe J BLANC | 1996 | Biotechnology Letters1996,18,2: | 1 |
| 17 | characterization of the Tea Fungus Metabol ites 显示文摘 | Philippe J BLANC | 1996 | Biotechnology Letters1996,18,2: | 1 |
| 18 | Interest of thoracic ultrasound after cardiac surgery or interventional cardiology显示文摘Thoracic ultrasound has attracted much interest in detecting pleural effusion or pulmonary consolidation after cardiac surgery.In 2016,Trovato reported,in the World Journal of Cardiology,the interest of using,in addition to echocardiography,thoracic ultrasound.In this editorial,we highlight the value of assessing diaphragm function after cardiac surgery and interventional cardiology pro-cedures.Various factors are able to impair diaphragm function after such interventions.Diaphragm motion may be decreased by chest pain secondary to sternotomy,pleural effusion or impaired muscle function.Hemidiaphragmatic paralysis may be secondary to phrenic nerve damage complicating cardiac surgery or atrial fibrillation ablation.Diagnosis may be delayed.Indeed,respi-ratory troubles induced by diaphragm dysfunction are frequently attributed to pre-existing heart disease or pulmonary complications secondary to surgery.In addition,elevated hemidiaphragm secondary to diaphragm dysfunction is sometimes not observed on chest X-ray performed in supine position in the intensive care unit.Analysis of diaphragm function by ultrasound during the recovery period appears essential.Both hemidiaphragms can be studied by two complementary ultrasound methods.The mobility of each hemidiaphragms is measured by M-mode ultrasonography.In addition,recording the percentage of inspiratory thickening provides important information about the quality of muscle function.These two approaches make it possible to detect hemidiaphragm paralysis or dysfunction.Such a diagnosis is important because persistent diaphragm dysfunction after cardiac surgery has been shown to be associated with adverse respiratory outcome.Early respiratory physio-therapy is able to improve respiratory function through strengthening of the inspiratory muscles i.e.diaphragm and accessory inspiratory muscles. | Martin Boussuges Philippe Blanc Fabienne Bregeon Alain Boussuges | 2024 | World Journal of Cardiology2024,16,3: | 0 |