Confirmed the correct cloning of MAG_5040 sequence into the vector. To

Confirmed the correct cloning of MAG_5040 sequence into the vector. To avoid the expression of truncated proteins, 7 mycoplasma TGA tryptophan codons contained in MAG_5040 were mutagenized to TGG by using the QuikChangeH Site-Directed Mutagenesis Kit (Stratagene), following Benzocaine site manufacturer’s instructions. Primers used for mutagenesis (MAG_5040/MUT) are summarized in Table S1. The final vector (pGEX-2T/rMAG_5040) Pentagastrin containing the mutagenized MAG_5040 gene was extracted as described above and sequenced. E. coli BL21(DE3) were transformed with pGEX-2T/ rMAG_5040 by means of RapidTransitTM Transformation Kit (Sigma-Aldrich) according to manufacturer’s instructions, and positive clones were selected for ampicillin and chloramphenicol resistance. Expression of rMAG_5040 was induced by adding IPTG (0.1 mM final concentration) and incubating at 30uC under constant agitation for 4 hours. The rGST-MAG_5040 fusion protein was purified by means of affinity chromatography with Glutathione SepharoseTM High Performance (GE Healthcare), and buffer-exchanged to PBS in a 30 kDa NMWL Amicon Ultra15 centrifugal filter unit (Millipore). In order to obtain rMAG_5040, GST was cleaved from rGST-MAG_5040 by using thrombin (GE Healthcare). Both rGST-MAG_5040 and rMAG_5040 concentrations were evaluated with the BCA Protein Assay kit (Pierce).Nuclease Activity AssaysApproximately 4 mg of rGST-MAG_5040 were incubated at 37uC in 100 ml reaction buffer (25 mM Tris-HCl, pH 8.8, 5 mM MgCl2, 5 mM CaCl2) containing 1 to 5 mg of nucleic acid substrate. Aliquots (10 ml) were sampled at different times of incubation, and reaction was stopped in each collected tube by adding EDTA at the final concentration of 20 mM. Digestion products were analyzed by agarose gel electrophoresis and documented as described above. Exonuclease and endonuclease activities were evaluated by digesting both linear DNA (UltraPureTM Calf Thymus DNA Solution, Invitrogen) and the circular plasmid pGEX-2T/rMAG_5040. Substrate specificity was investigated with ssDNA (M13 DNA, New England Biolabs) and total RNA purified from mid-log E. coli cultures. Optimal reaction conditions were defined by varying calcium and magnesium concentrations, ionic strength, and temperature in triplicate digestion reactions of the plasmid pGEX-2T/rMAG_5040. In order to examine the nuclease activity of rGST-MAG_5040 in the absence of exogenously supplied divalent cations, EDTA was added to the reaction (5 mM final concentration). In order to rule out carryover of E. coli nucleases along with the fusion protein, GST was expressed in E. coli, purified, and used as a negative control in all assays.Bacterial Strains and Culture ConditionsM. agalactiae PG2T was grown in PPLO medium supplemented with 20 heat inactivated horse serum and 500 mg/ml ampicillin, at 37uC with constant agitation. Mycoplasmas were collected by centrifugation (10 min at 10,0006g at 4uC), and washed three times with ice-cold PBS. Pellets were stored at 280uC until use. E. coli strains were grown in Luria-Bertani broth or on Luria-Bertani agar [28].Cloning, Expression, and Purification of rMAG_Total DNA DNeasy Blood MAG_5040 in a version of the was extracted from mycoplasma pellets with Tissue Kit (Qiagen). In order to express 1326631 fusion with glutathione-S-transferase (GST), MAG_5040 gene excluding the region encodingM. agalactiae SNaseLongitudinal Study and Sera CollectionTen sheep were selected from a Contagious Agalactia (CA) free flock in North Sardinia (Italy.Confirmed the correct cloning of MAG_5040 sequence into the vector. To avoid the expression of truncated proteins, 7 mycoplasma TGA tryptophan codons contained in MAG_5040 were mutagenized to TGG by using the QuikChangeH Site-Directed Mutagenesis Kit (Stratagene), following manufacturer’s instructions. Primers used for mutagenesis (MAG_5040/MUT) are summarized in Table S1. The final vector (pGEX-2T/rMAG_5040) containing the mutagenized MAG_5040 gene was extracted as described above and sequenced. E. coli BL21(DE3) were transformed with pGEX-2T/ rMAG_5040 by means of RapidTransitTM Transformation Kit (Sigma-Aldrich) according to manufacturer’s instructions, and positive clones were selected for ampicillin and chloramphenicol resistance. Expression of rMAG_5040 was induced by adding IPTG (0.1 mM final concentration) and incubating at 30uC under constant agitation for 4 hours. The rGST-MAG_5040 fusion protein was purified by means of affinity chromatography with Glutathione SepharoseTM High Performance (GE Healthcare), and buffer-exchanged to PBS in a 30 kDa NMWL Amicon Ultra15 centrifugal filter unit (Millipore). In order to obtain rMAG_5040, GST was cleaved from rGST-MAG_5040 by using thrombin (GE Healthcare). Both rGST-MAG_5040 and rMAG_5040 concentrations were evaluated with the BCA Protein Assay kit (Pierce).Nuclease Activity AssaysApproximately 4 mg of rGST-MAG_5040 were incubated at 37uC in 100 ml reaction buffer (25 mM Tris-HCl, pH 8.8, 5 mM MgCl2, 5 mM CaCl2) containing 1 to 5 mg of nucleic acid substrate. Aliquots (10 ml) were sampled at different times of incubation, and reaction was stopped in each collected tube by adding EDTA at the final concentration of 20 mM. Digestion products were analyzed by agarose gel electrophoresis and documented as described above. Exonuclease and endonuclease activities were evaluated by digesting both linear DNA (UltraPureTM Calf Thymus DNA Solution, Invitrogen) and the circular plasmid pGEX-2T/rMAG_5040. Substrate specificity was investigated with ssDNA (M13 DNA, New England Biolabs) and total RNA purified from mid-log E. coli cultures. Optimal reaction conditions were defined by varying calcium and magnesium concentrations, ionic strength, and temperature in triplicate digestion reactions of the plasmid pGEX-2T/rMAG_5040. In order to examine the nuclease activity of rGST-MAG_5040 in the absence of exogenously supplied divalent cations, EDTA was added to the reaction (5 mM final concentration). In order to rule out carryover of E. coli nucleases along with the fusion protein, GST was expressed in E. coli, purified, and used as a negative control in all assays.Bacterial Strains and Culture ConditionsM. agalactiae PG2T was grown in PPLO medium supplemented with 20 heat inactivated horse serum and 500 mg/ml ampicillin, at 37uC with constant agitation. Mycoplasmas were collected by centrifugation (10 min at 10,0006g at 4uC), and washed three times with ice-cold PBS. Pellets were stored at 280uC until use. E. coli strains were grown in Luria-Bertani broth or on Luria-Bertani agar [28].Cloning, Expression, and Purification of rMAG_Total DNA DNeasy Blood MAG_5040 in a version of the was extracted from mycoplasma pellets with Tissue Kit (Qiagen). In order to express 1326631 fusion with glutathione-S-transferase (GST), MAG_5040 gene excluding the region encodingM. agalactiae SNaseLongitudinal Study and Sera CollectionTen sheep were selected from a Contagious Agalactia (CA) free flock in North Sardinia (Italy.