Characterization of a glucansucrase from Lactobacillus reuteri E81 and production of malto-oligosaccharides
Özet
Glucansucrases, which can be produced by different Lactic Acid Bacteria (LAB), catalyze the synthesis of α-glucans with different structures and properties using sucrose as substrate. In this study, a novel glucansucrase (GTFA) from Lactobacillus reuteri E81 was identified and heterologously expressed. Alignments of GTFA with other glucansucrases revealed its novelty and a putative 3D model structure was obtained. The biochemical properties of the truncated enzyme without the N-terminal variable region, GTFA-ΔN, was characterized. The Km and Vmax were found to be 7.5 mM and 1.49 IU/mg, respectively, and it showed optimum activities at pH 7 and at 50 °C. The GTFA-ΔN produced in vitro an α-glucan with (α1 → 3) and (α1 → 6) glycosidic linkages using sucrose as the substrate. Importantly, GTFA-ΔN synthesized DP = 9 oligosaccharides using sucrose and maltose as the donor and acceptor sugars, respectively, as detected by TLC, HPLC, LC-MS and NMR analysis.
Anahtar Kelimeler
- Scopus
- 40
- WoS
- 40
- OpenAlex
- 40
Tam Kayıt
| Alan | Değer | Dil |
|---|---|---|
| dc.contributor.author | İspirli, Hümeyra | |
| dc.contributor.author | Yüzer, Mustafa Onur | |
| dc.contributor.author | Skory, Christopher | |
| dc.contributor.author | Colquhoun, Ian J. | |
| dc.contributor.author | Sağdıç, Osman | |
| dc.contributor.author | Dertli, Enes | |
| dc.date.accessioned | 2026-10-29T19:11:10.867994462Z | |
| dc.date.available | 2026-10-29T19:11:10.867994462Z | |
| dc.date.issued | 2019 | |
| dc.description.abstract | Glucansucrases, which can be produced by different Lactic Acid Bacteria (LAB), catalyze the synthesis of α-glucans with different structures and properties using sucrose as substrate. In this study, a novel glucansucrase (GTFA) from Lactobacillus reuteri E81 was identified and heterologously expressed. Alignments of GTFA with other glucansucrases revealed its novelty and a putative 3D model structure was obtained. The biochemical properties of the truncated enzyme without the N-terminal variable region, GTFA-ΔN, was characterized. The Km and Vmax were found to be 7.5 mM and 1.49 IU/mg, respectively, and it showed optimum activities at pH 7 and at 50 °C. The GTFA-ΔN produced in vitro an α-glucan with (α1 → 3) and (α1 → 6) glycosidic linkages using sucrose as the substrate. Importantly, GTFA-ΔN synthesized DP = 9 oligosaccharides using sucrose and maltose as the donor and acceptor sugars, respectively, as detected by TLC, HPLC, LC-MS and NMR analysis. | |
| dc.description.sponsorship | TUBITAK [116O523] | |
| dc.identifier.doi | 10.1080/10242422.2019.1593969 | |
| dc.identifier.eissn | 1029-2446 | |
| dc.identifier.endpage | 430 | |
| dc.identifier.issn | 1024-2422 | |
| dc.identifier.issue | 6 | |
| dc.identifier.scopus | 2-s2.0-85065527836 | |
| dc.identifier.startpage | 421 | |
| dc.identifier.uri | https://rdlopen.rawdatalibrary.net/r/bayburt/13584 | |
| dc.identifier.volume | 37 | |
| dc.identifier.wos | WOS:000469706400001 | |
| dc.language.iso | en | |
| dc.publisher | Taylor and Francis Ltd | |
| dc.relation.ispartof | Biocatalysis and Biotransformation | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.subject | glucan | |
| dc.subject | Glucansucrase | |
| dc.subject | malto-oligosaccharides | |
| dc.subject.classification | Biochemistry & Molecular Biology | |
| dc.subject.classification | Biotechnology & Applied Microbiology | |
| dc.subject.other | 3D modeling | |
| dc.subject.other | Lactic acid | |
| dc.subject.other | Sugar (sucrose) | |
| dc.subject.other | bacterial enzyme | |
| dc.subject.other | carbohydrate | |
| dc.subject.other | glucan | |
| dc.subject.other | glucansucrase | |
| dc.subject.other | maltooligosaccharide | |
| dc.subject.other | maltose | |
| dc.subject.other | oligosaccharide | |
| dc.subject.other | sucrose | |
| dc.subject.other | unclassified drug | |
| dc.subject.other | Biochemical properties | |
| dc.subject.other | Different structure | |
| dc.subject.other | Glycosidic linkages | |
| dc.subject.other | Lactic acid bacteria | |
| dc.subject.other | Lactobacillus reuteri | |
| dc.subject.other | Maltooligosaccharides | |
| dc.subject.other | amino terminal sequence | |
| dc.subject.other | Article | |
| dc.subject.other | biochemical analysis | |
| dc.subject.other | biotechnological production | |
| dc.subject.other | controlled study | |
| dc.subject.other | enzyme activity | |
| dc.subject.other | enzyme substrate | |
| dc.subject.other | high performance liquid chromatography | |
| dc.subject.other | in vitro study | |
| dc.subject.other | liquid chromatography-mass spectrometry | |
| dc.subject.other | model | |
| dc.subject.other | nonhuman | |
| dc.subject.other | nuclear magnetic resonance | |
| dc.subject.other | pH | |
| dc.subject.other | temperature | |
| dc.subject.other | thin layer chromatography | |
| dc.subject.other | Oligosaccharides | |
| dc.title | Characterization of a glucansucrase from Lactobacillus reuteri E81 and production of malto-oligosaccharides | |
| dc.type | Article | |
| rdl.citation.openalex | 40 | |
| rdl.citation.scopus | 40 | |
| rdl.citation.wos | 40 | |
| rdl.oa.status | closed | |
| rdl.oa.status | green | |
| rdl.oa.url | http://hdl.handle.net/20.500.12403/3076 | |
| rdl.scopus.quartile | Q3 | |
| rdl.source.index | SCOPUS | |
| rdl.source.index | WOS | |
| rdl.wos.index | Science Citation Index Expanded (SCI-EXPANDED) |
