کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
10235299 | 45028 | 2014 | 16 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Cloning, purification and characterization of translationally fused protein DNA methyltransferase Mâ¢HhaI-EGFP
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کلمات کلیدی
موضوعات مرتبط
مهندسی و علوم پایه
مهندسی شیمی
بیو مهندسی (مهندسی زیستی)
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چکیده انگلیسی
Design of the transcriptionally-fused protein M
- HhaI-EGFP, composed of bacterial DNA-methyltransferase M
- HhaI and enhanced green fluorescent protein (GFP) is described. The mentioned M
- HhaI-EGFP was expressed in Escherichia coli ER1821 and purified by affinity chromatography on Ni-NTA agarose. According to expectations M
- HhaI-EGFP fused protein retained significant features of corresponding original proteins: the ability to transfer methyl group to the C5 carbon atom of internal cytosine in CGCG site and absorption-emission spectral characteristics. The created transcriptionally-fused protein M
- HhaI-EGFP could be used in various experiments in molecular biology.
- HhaI-EGFP, composed of bacterial DNA-methyltransferase M
- HhaI and enhanced green fluorescent protein (GFP) is described. The mentioned M
- HhaI-EGFP was expressed in Escherichia coli ER1821 and purified by affinity chromatography on Ni-NTA agarose. According to expectations M
- HhaI-EGFP fused protein retained significant features of corresponding original proteins: the ability to transfer methyl group to the C5 carbon atom of internal cytosine in CGCG site and absorption-emission spectral characteristics. The created transcriptionally-fused protein M
- HhaI-EGFP could be used in various experiments in molecular biology.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Process Biochemistry - Volume 49, Issue 12, December 2014, Pages 2170-2173
Journal: Process Biochemistry - Volume 49, Issue 12, December 2014, Pages 2170-2173
نویسندگان
S.V. Tarlachkov, O.V. Dyachenko, A.M. Cherevatenko, N.V. Rudenko, T.V. Shevchuk,