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دراسة بعض الخصائص الفيزيائية والكيميائية لانزيم Staphylolysin المنتج من بكتريا Pseudomonas aeruginosa == Study of Some Physical and Chemical properties of Staphylolysin produced by Pseudomonas aeruginosa

Author name: شيماء سهيل نجم
Supervisor name: مي طالب فليح
General topic: Biology
Specific topic: Microbiology - Enzymes
Degree: Master
University: University of Baghdad
Language: Arabic
University location: Baghdad
First pages:
Abstract: عزلت (50) عزلة عائدة لبكتريا Pseudomonas aeruginosa من 120 عينة سريرية جمعت من مصادر مختلفة تضمنت (الادرار،والقشع ،والبراز ،ومسحات الاذن ، والجروح،والحروق).تم التحري عن انتاج بعض من عوامل الضراوة للعزلات قيد الدراسة مثل : الهيمولايسين، والايلاستيز ، والبروتيز ، ووجد ان نسبة انتاج الهيمولايسين والايلاستيز كانت 76% ، فيما كانت نسبة انتاج البروتيز 72% في العزلات المحلية قيد الدراسة.اختبرت قابلية العزلات المحلية على انتاج انزيم الستافيلولايسين ، وبينت نتائج الغربلة شبه الكمية ان 18 عزلة (36%) من العزلات لها القابلية على انتاج الانزيم وبنسب متفاوتة،اذ تراوحت اقطار الهالة الشفافة من(5 - 22)ملم ، وتميزت خمس عزلات منها باعطاءها اوسع مناطق تحلل على وسط ] ترتبك صويا الصلب + 0.2% (وزن/حجم) من بكتريا Staphylococcus aureus المعزولة المقتولة بالحرارة بدرجة 100م [تراوحت من (16 - 22)ملم ، وتم انتخاب العزلة 16P لاستخلاص الستافيلولايسين A (LasA) ، اذ بلغت الفعالية النوعية لها (8.59)وحدة / ملغم بروتين ، والعزلة 5P لاستخلاص الستافيلولايسين D (LasD)، اذ بلغت الفعالية النوعية لها (0.66)وحدة / ملغم بروتين ،لكونهما الاغزر انتاجا للانزيم عند اجراء الغربلة الكمية.استخلص انزيم الستافيلولايسين بالنبذ المركزي المبرد وتمت تنقيته جزئيا بترسيبه بكبريتات الامونيوم بنسبة اشباع 80% ثم بكروموتوغرافيا التبادل الايوني باستخدام المبادل DEAE - Cellulose ، بينت النتائج ان الفعالية الانزيمية الحالة للعنقوديات (Staphylolytic activity) لانزيم الستافيلولايسين A ظهرت في القمة الاولى، وبلغت عدد مرات التنقية 10.74 مرة وبحصيلة انزيمية 14.2%،فيما اظهرت القمة الثانية الفعالية الانزيمية الحالة للعنقوديات لانزيم الستافيلولايسين D بعدد مرات تنقية 9.1 مرة وبحصيلة انزيمية 18.14%.درست بعض خصائص الانزيمين فكان الوزن الجزيئي 20.417 كيلو دالتون و23.988 كيلو دالتون للستافيلولايسين D,A على التوالي عند تقديرهما بطريقة الترحيل الكهربائي في هلام SDS - PAGE. لوحظ ان الرقم الهيدروجيني الامثل لفعالية الستافيلولايسين A هو 8 اذ اعطى اعلى فعالية بلغت 150 وحدة / مل ، ولثبات الانزيم 7.5 - 8.5 اذ احتفظ الانزيم بكامل فعاليته تقريبا ، فيما كان الرقم الهيدروجيني الامثل لفعالية الستافيلولايسين D هو 9.5 اذ اعطى اعلى فعالية بلغت 16 وحدة / مل ، ولثبات الانزيم 8.5 - 9.5 اذ احتفظ الانزيم بكامل فعاليته تقريبا ، وظهرت اقصى فعالية للانزيمين عند درجة حرارة 40م اذ بلغت الفعالية النوعية للستافيلولايسين A 140 وحدة /مل وللستافيلولايسين D 16.4 وحدة/ مل ، واحتفظ كلا الانزيمين بكامل فعاليتهما تقريبا عند حضنهما بدرجة حرارة 25 - 40م لمدة ساعة.عند دراسة تاثير بعض المواد في الفعالية الانزيمية للستافيلولايسين D,A كان لكلوريد الصوديوم وكلوريد البوتاسيوم بتركيز 1 و5 ملي مولار تاثير منشط للفعالية الانزيمية قياسا بالسيطرة اذ احتفظ انزيم الستافيلولايسين A بـ105% و108% من فعاليته على التوالي عند معاملته بكلوريد الصوديوم ، واحتفظ بـ 102% و104% من فعاليته على التوالي عند معاملته بكلوريد البوتاسيوم، في حين ثبطت الفعالية الانزيمية عند معاملتهما بكلوريدات الحديد والزئبق والخارصين وبنسب متفاوتة ،اذ احتفظ انزيم الستافيلولايسين A بـ 73% و7% من فعاليته على التوالي عند معاملته بـ5ملي مولار من كلوريد الحديد والزئبق على التوالي،و9% فقط من فعاليته عند معاملته بـ 0.1 ملي مولار من كلوريد الخارصين ، فيما احتفظ انزيم الستافيلولايسين D بـ45% و13% من فعاليته فقط عند معاملته بـ5 ملي مولار من كلوريد الحديد والزئبق على التوالي،و23% فقط من فعاليته عند معاملته بـ0.1 ملي مولار من كلوريد الخارصين، بينما احتفظ كلا الانزيمين بكامل فعاليتهما عند المعاملة بمادة EDTA بتركيز 10 ملي مولار ،وفنيل مثيل سلفونيل فلورايد (PMSF) بتركيز 0.4 ملي مولار. | Fifty isolates of Pseudomonas aeruginosa were obtained from 120 various clinical samples included (urine, sputum, stool, ear, wound & burn swabs). Detection of the production of some virulence factors (hemolysin, elastase and protease) by the local isolates was studied. Results showed that the hemolysin and elastase production ratio were 76%, while the protease production ratio was about 72% by the local isolates.Detection of the ability of local isolates to produce staphylolysin enzyme was studied, the semi quantity screening results showed that 18 (36%) of the isolates have the ability to produce this enzyme in variable ratios , the diameters of lysis Zone ranged from(5 - 22)mm, and five isolates were characterized by giving the highest lysis zone on (Tryptic soya agar + 0.2% (wt./vol.) of heat killed Staphylococcus. aureus at temperature 100oC ) medium which were ranged from(16 - 22)mm, then the isolate P16 was chosen to extract staphylolysin A (LasA) and it's specific activity reaches 8.59 unit /mg protein, whi1e chosen the isolate P5 to extract staphylolysin D (LasD) where it's specific activity reaches 0.66 unit /mg protein since the two isolates were the most production of enzyme by quantity screening . Staphylolysin enzyme was extracted by cooling centrifugation and partially purified by ammonium sulphate precipitation in saturation percentage of 80%, this step was followed by Ion exchange chromatography technique by using DEAE - cellulose column, results showed that the enzymatic activity (Staphylolytic activity) of the staphylolysin A appeared in first peak with purification folds and recovery of 10.74 fold and 14.2% respectively, while the second peak appeared the activity for staphylolysin D with purification folds and recovery of 9.1 fold and 18.14% respectively.Some of the characters of the two enzymes were studied, so the molecular weights were 20.417 kilo dalton & 23.988 kilo dalton for staphylolysin A&D respectively were estimated by SDS - polyacryl amide gel e1ectrophoresis. The optimum pH for staphylolysin A activity was found to be 8 which gives higher activity reaches 150 unit/ml, and for enzyme stability was 7.5 - 8.5 in which the enzyme nearly retained it's full activity, while there were for staphylolysin D 9.5 that gives higher activity of 16 unit/ml.& 8.5 - 9.5 in which the enzyme nearly retained it's full activity respectively, Maximum activity of two enzymes was obtained at 40 C in which the specific activity were for staphylolysin A and D 140 and 16.4 unit/ml , and the activity for two enzymes at 25 - 40 C remained approximately without change for one hour. When the effects of some materials on staphylolysin A & D activity were studied, the results showed that both sodium chloride & potassium chloride at 1 & 5 mM had the activator effect on enzymatic activity compared with its control where the staphylolysin A and D retained 105% ,108% and 102%, 104% of their activity, respectively when treated with sodium chloride, while they retained 110%, 114% and 133%, 118% of their activity, respectivity when treated with potassium chloride, while ferric, mercury & zinc chlorides inhibited the activity in variable ratios in which the staphylolysin A and D kept only 73%, 7% and 45%, 13% respectively of their initial activity when treated with 5mM of ferric and meracury chloride and 9%, 23% respectively of their initial activity when treated with 0.1mM zinc chlorid & enzymatic activity for both enzymes were not affected when treated with EDTA at 10mM & phenyl methyl sulphonyl fluoride (PMSF) at 0.4mM.

تعيين بعض الظروف الزرعية لانتاج انزيم السليليز والكحول الاثيلي من بعض انواع البكتريا المعزولة من التربة == Determination of Some Cultural Conditions For Cellulase And Ethanol Production By Bacteria Isolated From Soil

Author name: عبد الستار عبد الجبار ابراهيم
Supervisor name: عدنان نعمة عبد الرضا العزاوي | انيس عبد الله كاظم
General topic: Biology
Specific topic: Microbiology - Enzymes
Degree: Master
Language: Arabic
University location: Diyala
First pages:
Abstract: The study included isolate and diagnose of some types of anaerobic and aerobic bacteria capable of decomposing and fermentation of cellulose. Isolation and diagnose the bacteria Clostridium phytofermentous from 10 agricultural soil samples, was 50 % of the total 50 colony, while isolation of Escherichia coli from 15 waste water samples which represented 40% of the total 75 colony and isolated Pseudomonas aeruginosa from 15 normal soil samples, and was 53% of the total 75 colony. production of cellulase enzymes was evaluated by using absorbance method. Higher activity obtained via Clostridium phytofermentous with maximum value of 42.8 IU / mL, while Pseudomonas aeruginosa gives 12.5 IU / mL and Escherichia coli gives 29.1 IU / mL.. Optimum temperature was 35 C and pH 7, for production cellulose enzyme The concentration of ethanol Alcohol was measured by using Titration method. Maximum concentration of ethanol alcohol produced by Escherichia coli, which reached 8.28 g/liter, while Pseudomonas aeruginosa was 7.86 g/liter, and Clostridium phytofermentous reached 6.62 g/L.

دراسة جزيئية لعوامل ضراوة المكورات النعقودية السالبة لانزيم التجليط والمعزولة من اصابات مختلفة == Molecular Study of Virulence Factors of Some Coagulase Negative Staphylococci Isolated From Different Infections

Author name: سعاد عبد الهادي عبد الرزاق الحلو
Supervisor name: عباس شاكر جواد المحنة
General topic: Biology
Specific topic: Microbiology - Enzymes
Degree: Doctorate
Language: English
University location: Najaf
First pages:
Abstract: The study aimed to investigating the role of coagulase - negative staphylococci in human infections, and determining the predominance genes of the virulence factors. Three hundred clinical specimens were collected from out and inpatients undergoing catheter related infections and twenty specimens were collected from healthy hospital staff as a control from January 2013 to July 2013 of Al - Zahraa Teaching Hospital, Al - Sader Teaching Hospital and Al - Hakeem Hospital in Al - Najaf Al - Ashraf province. The specimens were included urine, blood, vaginal swabs, seminal fluid and wound swabs. The specimens were cultured on mannitol salt agar and the primary identification was depended on Gram stained and biochemical tests. Then finally identification with Vitek 2 system is done.One hundred isolates were identified as coagulase - negative staphylococci (CoNS), Staphylococcus haemolyticus was identified as the most frequently isolated species in (53%), followed by Staphylococcus epidermidis (26%) and Staphylococcus hominis were recorded in (21%). Most of CoNS isolates were highly resistance to penicillin G (benzylpenicillin), oxacillin, cefoxitin and erythromycin; and low resistance to rifampicin, levofloxacin and others. While, control isolates results showed moderate resistance to penicillin G and erythromycin; low - level of resistance to cefoxitin, oxacillin and other antibiotics.The investigation of virulence factors revealed that 93% of coagulase - negative staphylococci isolates were production of slime layer, DNase 58%, protease 29% and hemolysin 88%. But the results gave negative result for TNase and lipase enzymes.Monoplex and multiplex PCR were used to explore the MecA, aap, icaA, icaD, atlE, sea, seb, sec, sed, hla, hlb, sspA, sspB, geh, nuc genes. The results showed that all CoNS isolates (100%) had mecA and atlEgenes, but 98% of isolates had aap, 93% icaA and icaD genes. PCR revealed that only (14%) of isolates had genes for enterotoxins expression. (92.86%) and (7.14%), sea and seb respectively, in contrast, the sec and sed genes were not be recorded.The result showed that 47% of CoNS isolates had hla gene and 41% contain hlb gene, 29% were positive for the sspA gene whereas the sspB gene and geh and nuc2 genes not found in any of staphylococcal isolates. Finally, the result indicated that 58% of CoNS isolates were expressed the nuc1 gene.Plasmid curing was carried out in order to determine the origin of resistance and some virulence factor genes (chromosomal or plasmid - borne gene). The curing (elimination) of the plasmids of coagulase - negative staphylococci isolated was catalyzed using ethidium bromide in different concentration and high temperature (44?C). The results showed that the oxacillin resistant coagulase - negative staphylococci were plasmid mediated since 93% of the isolates showed negative result on oxacillin resistance screening agar, and absence of mecA gene from all isolates. Also, 41 of coagulase - negative staphylococci isolates that showed ? - hemolysin became non - hemolysin after manipulated with ethidium bromide.Finelly, taking into consideration the etiological importance of CoNS has often been neglected, the present investigation confirmed that these microorganisms should not be ignored or classified as mere contaminant.

استنسال,تعبيـر ,تنـقية وتوصيف الجديد والمعزول من L-glutamin-(asparagin-)ase Klebsiella pneumoniae MGH 78578 == Cloning, Expression, Purification, And Characterization Of Novel L-Glutamin- (Asparagin-)Ase From Klebsiella Pneumoniae Mgh78578

Author name: مها حميد عبد الله البحراني
Supervisor name: غازي منعم عزيز | عبد الكريم عبد الرزاق
General topic: Biology
Specific topic: Microbiology - Enzymes
Degree: Doctorate
University: University of Baghdad
Language: English
University location: Baghdad
First pages:

انتاج انزيم الانيولينيز من الفطر Rhizopus oryzae بوساطة تخمرات الحالة الصلبة ودوره في انتاج قليلات السكريد الفركتوزي

Author name: قيس مجيد عيسى العكيدي
Supervisor name: منى حمودي الجبوري | عبد الكريم جاسم هاشم
General topic: Biology
Specific topic: Microbiology - Enzymes
Degree: Master
University: University of Baghdad
Language: Arabic
University location: Baghdad
First pages:

استخلاص وتوصيف انزيم اليوريز من بكتريا المتقلبات المعزولة من مرضى خمج المجاري البولية في اليمن == Extraction And Characterization Of Urease Enzyme Of Proteus spp. Isolated From Patients With Urinary Tract Infection In Yemen

Author name: سعيد محمد عوض اسماعيل
Supervisor name: حسين حسن خانقاه | عصام فاضل الجميلي
General topic: Biology
Specific topic: Microbiology - Enzymes
Degree: Doctorate
Language: Arabic
University location: Baghdad
First pages:
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