2014
DOI: 10.1134/s0003683814030168
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Molecular mutagenesis at Tyr-101 of the amylomaltase transcribed from a gene isolated from soil DNA

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Cited by 7 publications
(4 citation statements)
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“…This isolated gene had a high amino acid sequence identity to amylomaltase of Thermus thermophilus [17]. The expression of both recombinant enzymes was induced by 0.8 mM IPTG when A 600 of the culture reached 0.5.…”
Section: Amylomaltase Preparationmentioning
confidence: 99%
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“…This isolated gene had a high amino acid sequence identity to amylomaltase of Thermus thermophilus [17]. The expression of both recombinant enzymes was induced by 0.8 mM IPTG when A 600 of the culture reached 0.5.…”
Section: Amylomaltase Preparationmentioning
confidence: 99%
“…The recombinant plasmids containing WT-and Y101S-amylomaltase genes were expressed in E. coli BL21 (DE3) [17], and the obtained enzymes were purified by a Ni-NTA column. The specific activity of the mutated enzyme for the cyclization reaction showed a small increase, while significant decreases in the starch transglycosylation, disproportionation, coupling, and hydrolytic activities were observed (Table 1).…”
Section: Amylomaltase Preparationmentioning
confidence: 99%
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“…Tyr54 and Tyr101 278 (T. aquaticus amylomaltase numbering [9]), since both were identified 279 as the aromatic positions involved in the secondary glucan-binding 280 site of the enzyme[49,57,58]. While the former was determined to con-281 trol the hydrolytic activity[57,59], the latter was shown to be responsi-282 ble rather for disproportionating activity of the amylomaltase[58,60].283 Interestingly, the residues of the secondary glucan-binding site from 284 T. aquaticus amylomaltase were found to be not strictly conserved 285 among its counterparts [27,61]. A detailed inspection of the alignment 286 of all 416 4-α-glucanotransferases compared in the present study con-287 firmed that neither Tyr54, nor Tyr101 does represent a conserved posi-288 tion in the family GH77 (Fig.…”
mentioning
confidence: 99%