Sucrose synthase from rice grains was purified using anion exchange techniques and preparative gel filtration. In order to utilize the enzyme in subsequent enzymatic syntheses of nucleotide sugars the purification protocol was optimized to yield an enzyme preparation which is free of phosphatases hydrolysing nucleotides. The enzyme preparation was investigated by SDS polyacrylamide gel-electrophoresis (molecular mass of subunit 90 kDa) and isoelectric focusing (pI 6.16) with silver staining. The native enzyme is a tetrameric protein with a molecular mass of 362 kDa. Edman degradation revealed a blocked N-terminus.
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Konkuk Univ, Dept Biosci & Biotechnol, Bio Mol Informat Ctr, Seoul 143701, South KoreaKonkuk Univ, Dept Biosci & Biotechnol, Bio Mol Informat Ctr, Seoul 143701, South Korea
Lee, Yoon Jung
Kim, Jeong Ho
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Konkuk Univ, Dept Biosci & Biotechnol, Bio Mol Informat Ctr, Seoul 143701, South KoreaKonkuk Univ, Dept Biosci & Biotechnol, Bio Mol Informat Ctr, Seoul 143701, South Korea
Kim, Jeong Ho
Kim, Bong Gyu
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Konkuk Univ, Dept Biosci & Biotechnol, Bio Mol Informat Ctr, Seoul 143701, South KoreaKonkuk Univ, Dept Biosci & Biotechnol, Bio Mol Informat Ctr, Seoul 143701, South Korea
Kim, Bong Gyu
Lim, Yoongho
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Konkuk Univ, Dept Biosci & Biotechnol, Bio Mol Informat Ctr, Seoul 143701, South KoreaKonkuk Univ, Dept Biosci & Biotechnol, Bio Mol Informat Ctr, Seoul 143701, South Korea
Lim, Yoongho
Ahn, Joong-Hoon
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Konkuk Univ, Dept Biosci & Biotechnol, Bio Mol Informat Ctr, Seoul 143701, South KoreaKonkuk Univ, Dept Biosci & Biotechnol, Bio Mol Informat Ctr, Seoul 143701, South Korea