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Items: 1 to 20 of 100

1.
2.

Enzymatic synthesis of α-flavone glucoside via regioselective transglucosylation by amylosucrase from Deinococcus geothermalis.

Jang SW, Cho CH, Jung YS, Rha C, Nam TG, Kim DO, Lee YG, Baek NI, Park CS, Lee BH, Lee SY, Shin HS, Seo DH.

PLoS One. 2018 Nov 19;13(11):e0207466. doi: 10.1371/journal.pone.0207466. eCollection 2018.

3.

Enzymatic modification of daidzin using heterologously expressed amylosucrase in Bacillus subtilis.

Kim ER, Rha CS, Jung YS, Choi JM, Kim GT, Jung DH, Kim TJ, Seo DH, Kim DO, Park CS.

Food Sci Biotechnol. 2018 Aug 18;28(1):165-174. doi: 10.1007/s10068-018-0453-7. eCollection 2019 Feb.

PMID:
30815307
4.

Structural investigation of the thermostability and product specificity of amylosucrase from the bacterium Deinococcus geothermalis.

Guérin F, Barbe S, Pizzut-Serin S, Potocki-Véronèse G, Guieysse D, Guillet V, Monsan P, Mourey L, Remaud-Siméon M, André I, Tranier S.

J Biol Chem. 2012 Feb 24;287(9):6642-54. doi: 10.1074/jbc.M111.322917. Epub 2011 Dec 29.

5.

Fluorescence detection of the transglycosylation activity of amylosucrase.

Seo DH, Jung JH, Park CS.

Anal Biochem. 2017 Sep 1;532:19-25. doi: 10.1016/j.ab.2017.05.028. Epub 2017 May 31.

PMID:
28577993
6.

Evaluation of depigmenting activity by 8-hydroxydaidzein in mouse B16 melanoma cells and human volunteers.

Tai SS, Lin CG, Wu MH, Chang TS.

Int J Mol Sci. 2009 Nov 20;10(10):4257-66. doi: 10.3390/ijms10104257.

7.

Improved polymerization activity of Deinococcus geothermalis amylosucrase by semi-rational design: Effect of loop flexibility on the polymerization reaction.

Seo DH, Jung JH, Park CS.

Int J Biol Macromol. 2019 Jun 1;130:177-185. doi: 10.1016/j.ijbiomac.2019.02.139. Epub 2019 Feb 23.

PMID:
30807799
8.

Sustainable Production of Dihydroxybenzene Glucosides Using Immobilized Amylosucrase from Deinococcus geothermalis.

Lee HS, Kim TS, Parajuli P, Pandey RP, Sohng JK.

J Microbiol Biotechnol. 2018 Sep 28;28(9):1447-1456. doi: 10.4014/jmb.1805.05054.

9.

Synthesis and biological evaluation of a novel baicalein glycoside as an anti-inflammatory agent.

Kim KH, Park YD, Park H, Moon KO, Ha KT, Baek NI, Park CS, Joo M, Cha J.

Eur J Pharmacol. 2014 Dec 5;744:147-56. doi: 10.1016/j.ejphar.2014.10.013. Epub 2014 Oct 29.

PMID:
25446915
10.

Biosynthesis of (+)-catechin glycosides using recombinant amylosucrase from Deinococcus geothermalis DSM 11300.

Cho HK, Kim HH, Seo DH, Jung JH, Park JH, Baek NI, Kim MJ, Yoo SH, Cha J, Kim YR, Park CS.

Enzyme Microb Technol. 2011 Jul 10;49(2):246-53. doi: 10.1016/j.enzmictec.2011.05.007. Epub 2011 May 19.

PMID:
22112416
11.

Cloning, purification and characterization of a thermostable amylosucrase from Deinococcus geothermalis.

Emond S, Mondeil S, Jaziri K, André I, Monsan P, Remaud-Siméon M, Potocki-Véronèse G.

FEMS Microbiol Lett. 2008 Aug;285(1):25-32. doi: 10.1111/j.1574-6968.2008.01204.x. Epub 2008 Jun 3.

12.

Glycosylation Enhances the Physicochemical Properties of Caffeic Acid Phenethyl Ester.

Moon KO, Park S, Joo M, Ha KT, Baek NI, Park CS, Cha J.

J Microbiol Biotechnol. 2017 Nov 28;27(11):1916-1924. doi: 10.4014/jmb.1706.06017.

13.

High-efficiency enzymatic production of α-isoquercitrin glucosides by amylosucrase from Deinococcus geothermalis.

Rha CS, Choi JM, Jung YS, Kim ER, Ko MJ, Seo DH, Kim DO, Park CS.

Enzyme Microb Technol. 2019 Jan;120:84-90. doi: 10.1016/j.enzmictec.2018.10.006. Epub 2018 Oct 19.

PMID:
30396404
14.

An unusual chimeric amylosucrase generated by domain-swapping mutagenesis.

Seo DH, Jung JH, Jung DH, Park S, Yoo SH, Kim YR, Park CS.

Enzyme Microb Technol. 2016 May;86:7-16. doi: 10.1016/j.enzmictec.2016.01.004. Epub 2016 Jan 15.

PMID:
26992787
15.

Enzymatic synthesis of salicin glycosides through transglycosylation catalyzed by amylosucrases from Deinococcus geothermalis and Neisseria polysaccharea.

Jung JH, Seo DH, Ha SJ, Song MC, Cha J, Yoo SH, Kim TJ, Baek NI, Baik MY, Park CS.

Carbohydr Res. 2009 Sep 8;344(13):1612-9. doi: 10.1016/j.carres.2009.04.019. Epub 2009 Apr 22.

PMID:
19482267
16.

High-yield enzymatic bioconversion of hydroquinone to α-arbutin, a powerful skin lightening agent, by amylosucrase.

Seo DH, Jung JH, Ha SJ, Cho HK, Jung DH, Kim TJ, Baek NI, Yoo SH, Park CS.

Appl Microbiol Biotechnol. 2012 Jun;94(5):1189-97. doi: 10.1007/s00253-012-3905-7.

PMID:
22314516
17.
18.

Isolation, bioactivity, and production of ortho-hydroxydaidzein and ortho-hydroxygenistein.

Chang TS.

Int J Mol Sci. 2014 Apr 3;15(4):5699-716. doi: 10.3390/ijms15045699. Review.

19.

Insight into the structure, dynamics and the unfolding property of amylosucrases: implications of rational engineering on thermostability.

Liu M, Wang S, Sun T, Su J, Zhang Y, Yue J, Sun Z.

PLoS One. 2012;7(7):e40441. doi: 10.1371/journal.pone.0040441. Epub 2012 Jul 6.

20.

8-Hydroxydaidzein is unstable in alkaline solutions.

Chang TS.

J Cosmet Sci. 2009 May-Jun;60(3):353-7.

PMID:
19586603

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