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http://dx.doi.org/10.4014/jmb.1802.02021

Characterization of Ribose-5-Phosphate Isomerase B from Newly Isolated Strain Ochrobactrum sp. CSL1 Producing ʟ-Rhamnulose from ʟ-Rhamnose  

Shen, Min (School of Chemistry, Biology, and Material Engineering, Suzhou University of Science and Technology)
Ju, Xin (School of Chemistry, Biology, and Material Engineering, Suzhou University of Science and Technology)
Xu, Xinqi (Fujian Key Laboratory of Marine Enzyme Engineering, Fuzhou University)
Yao, Xuemei (School of Chemistry, Biology, and Material Engineering, Suzhou University of Science and Technology)
Li, Liangzhi (School of Chemistry, Biology, and Material Engineering, Suzhou University of Science and Technology)
Chen, Jiajia (School of Chemistry, Biology, and Material Engineering, Suzhou University of Science and Technology)
Hu, Cuiying (School of Chemistry, Biology, and Material Engineering, Suzhou University of Science and Technology)
Fu, Jiaolong (School of Chemistry, Biology, and Material Engineering, Suzhou University of Science and Technology)
Yan, Lishi (School of Chemistry, Biology, and Material Engineering, Suzhou University of Science and Technology)
Publication Information
Journal of Microbiology and Biotechnology / v.28, no.7, 2018 , pp. 1122-1132 More about this Journal
Abstract
In this study, we attempted to find new and efficient microbial enzymes for producing rare sugars. A ribose-5-phosphate isomerase B (OsRpiB) was cloned, overexpressed, and preliminarily purified successfully from a newly screened Ochrobactrum sp. CSL1, which could catalyze the isomerization reaction of rare sugars. A study of its substrate specificity showed that the cloned isomerase (OsRpiB) could effectively catalyze the conversion of $\text\tiny{L}$-rhamnose to $\text\tiny{L}$-rhamnulose, which was unconventional for RpiB. The optimal reaction conditions ($50^{\circ}C$, pH 8.0, and 1 mM $Ca^{2+}$) were obtained to maximize the potential of OsRpiB in preparing $\text\tiny{L}$-rhamnulose. The catalytic properties of OsRpiB, including $K_m$, $k_{cat}$, and catalytic efficiency ($k_{cat}/K_m$), were determined as 43.47 mM, $129.4sec^{-1}$, and 2.98 mM/sec. The highest conversion rate of $\text\tiny{L}$-rhamnose under the optimized conditions by OsRpiB could reach 26% after 4.5 h. To the best of our knowledge, this is the first successful attempt of the novel biotransformation of $\text\tiny{L}$-rhamnose to $\text\tiny{L}$-rhamnulose by OsRpiB biocatalysis.
Keywords
L-rhamnose; L-rhamnulose; Ochrobactrum sp. CSL1; rare sugar; ribose-5-phosphate isomerase B;
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