2005
DOI: 10.1128/jb.187.6.2002-2009.2005
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Substrate Specificities and Expression Patterns Reflect the Evolutionary Divergence of Maltose ABC Transporters in Thermotoga maritima

Abstract: Duplication of transporter genes is apparent in the genome sequence of the hyperthermophilic bacterium Thermotoga maritima. The physiological impacts of these duplications are not well understood, so we used the bacterium's two putative maltose transporters to begin a study of the evolutionary relationship between a transporter's function and the control of expression of its genes. We show that the substrate binding proteins encoded by these operons, MalE1 and MalE2, have different substrate specificities and … Show more

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Cited by 25 publications
(38 citation statements)
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References 35 publications
(50 reference statements)
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“…Carbohydrate utilization by T. maritima has been examined by studying the substrate specificities and affinities of its carbohydrate transporters (Nanavati et al 2005(Nanavati et al , 2006Cuneo et al 2009;Boucher and Noll 2011;Ghimire-Rijal et al 2014) and their transcriptional regulation in response to growth on different saccharides (Frock et al 2012). Information about substrate specificities, enzymatic activities, and catalytic mechanisms of many of T. maritima's glycoside hydrolases are also available (Kleine and Liebl 2006;Comfort et al 2007;Arti et al 2012), which has been used, for instance, to engineer an ␣-galactosidase from T. maritima into an efficient ␣-galactosynthase (Cobucci-Ponzano et al 2011).…”
Section: The Thermotogaementioning
confidence: 99%
“…Carbohydrate utilization by T. maritima has been examined by studying the substrate specificities and affinities of its carbohydrate transporters (Nanavati et al 2005(Nanavati et al , 2006Cuneo et al 2009;Boucher and Noll 2011;Ghimire-Rijal et al 2014) and their transcriptional regulation in response to growth on different saccharides (Frock et al 2012). Information about substrate specificities, enzymatic activities, and catalytic mechanisms of many of T. maritima's glycoside hydrolases are also available (Kleine and Liebl 2006;Comfort et al 2007;Arti et al 2012), which has been used, for instance, to engineer an ␣-galactosidase from T. maritima into an efficient ␣-galactosynthase (Cobucci-Ponzano et al 2011).…”
Section: The Thermotogaementioning
confidence: 99%
“…The complexity of its carbohydrate utilization strategies, revealed by genome sequencing (48) and through previous work (11,12,47,51), is surprising, given the primitive features of this microorganism. Considerable genomic plasticity has been observed even within the Thermotoga genus, with respect to the gene content of carbohydrate active enzymes and transporter subunits, which may to some extent relate to lateral gene transfer events (48,49).…”
mentioning
confidence: 99%
“…2; also see Table S3 in the supplemental material). MalE2 binds maltose, maltotriose, and trehalose with respective K d values of 8.4 M, 11 M, and 9.5 M, but mannotetraose was not a ligand (13). At 10 mM sugar, we observed that maltose and maltotriose increased the thermal stability of MalE2 with ⌬T m values of 1.02°C and 6.85°C, respectively, while the ⌬T m value in the presence of 10 mM mannotetraose was 0.24°C ( Fig.…”
Section: Resultsmentioning
confidence: 62%
“…These proteins were previously characterized and their apparent dissociation constants (K d ) were determined using fluorescence spectroscopy (13,23). Fig.…”
Section: Resultsmentioning
confidence: 99%
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