کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
34369 45020 2014 9 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Cloning, expression, purification and characterization of an oligomeric His-tagged thermophilic esterase from Thermus thermophilus HB27
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی بیو مهندسی (مهندسی زیستی)
پیش نمایش صفحه اول مقاله
Cloning, expression, purification and characterization of an oligomeric His-tagged thermophilic esterase from Thermus thermophilus HB27
چکیده انگلیسی


• A thermophilic membrane-associated esterase from Thermus thermophilus HB27 was expressed in Escherichia coli.
• E34Tt-His6 was purified from the E. coli membrane as a dimer in a single step by using metal affinity chromatography.
• Detergent was essential for activity and stability. The esterase had preference for short chain esters.
• The Rosso's model was used to describe the enzyme activity as a function of pH and temperature.
• Activity was maximal at 58 °C and pH 6.3. The enzyme was active in a wide temperature (19.7–79.4 °C) and pH range (4.0–9.3).

The esterase E34Tt (YP_004875.1) from Thermus thermophilus HB27 was cloned, expressed in Escherichia coli as a His-tagged protein, purified and characterized. The gene sequence was subcloned into a T-vector, released with the restriction enzymes BamHI and HindIII, ligated to a pET-21d(+) vector, and transferred to E. coli BL21 (DE3) cells. Inducer concentration (isopropyl β-d-1-thiogalactopyranoside, IPTG) and cultivation time before and after induction were optimized. Best results were obtained by adding 0.25 mM IPTG after 8 h of cultivation and maintaining the induction during 4 extra hours. Most of the enzyme (94%) remained membrane-associated and had to be extracted with a detergent. From the membrane crude extract, the His-tagged E34Tt was purified as a dimer (71.8 kDa) in a single purification step by using metal affinity chromatography. The Rosso's model was used to optimize the reaction conditions. E34Tt-His6 was active in a wide temperature (19.7–79.4 °C) and pH range (4.0–9.3), and maximal activity was determined at pH 6.3 and 58.2 °C, which is 10–18 °C higher than the optimal reaction temperature of the previously reported variants expressed in mesophilic yeasts. E34Tt-His6 preferentially hydrolyzed esters with ten carbon atoms, and was highly thermostable (half-life of 107.9 min at 85 °C), suggesting that E34Tt-His6 has potential for industrial applications.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Process Biochemistry - Volume 49, Issue 6, June 2014, Pages 927–935
نویسندگان
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