Hydrolysis of by-product adenosine diphosphate from 3′-phosphoadenosine-5′-phosphosulfate preparation using Nudix hydrolase NudJ

Verfasser / Beitragende:
[Feifei Bao, Huihui Yan, Hanju Sun, Peizhou Yang, Guoqing Liu, Xianxuan Zhou]
Ort, Verlag, Jahr:
2015
Enthalten in:
Applied Microbiology and Biotechnology, 99/24(2015-12-01), 10771-10778
Format:
Artikel (online)
ID: 605502730
LEADER caa a22 4500
001 605502730
003 CHVBK
005 20210128100607.0
007 cr unu---uuuuu
008 210128e20151201xx s 000 0 eng
024 7 0 |a 10.1007/s00253-015-6911-8  |2 doi 
035 |a (NATIONALLICENCE)springer-10.1007/s00253-015-6911-8 
245 0 0 |a Hydrolysis of by-product adenosine diphosphate from 3′-phosphoadenosine-5′-phosphosulfate preparation using Nudix hydrolase NudJ  |h [Elektronische Daten]  |c [Feifei Bao, Huihui Yan, Hanju Sun, Peizhou Yang, Guoqing Liu, Xianxuan Zhou] 
520 3 |a 3′-Phosphoadenosine-5′-phosphosulfate (PAPS) is the obligate cosubstrate and source of the sulfonate group in the chemoenzymatic synthesis of heparin, a clinically used anticoagulant drug. Previously, we have developed a method to synthesize PAPS with Escherichia coli crude extracts, which include three overexpressed enzymes and a fourth unidentified protein. The unknown protein degrades adenosine diphosphate (ADP), the by-product of PAPS synthesis reaction. To further understand and control the process of in vitro enzymatic PAPS synthesis, we decide to identify the fourth protein and develop a defined method to synthesize PAPS using purified enzymes. Here, we show that the purified Nudix hydrolase NudJ degrades ADP at high efficiency and serves as the fourth enzyme in PAPS synthesis. Under the defined condition of PAPS synthesis, all of the 10-mM ADP is hydrolyzed to form adenosine monophosphate (AMP) in a 15-min reaction. ADP is a better substrate for NudJ than adenosine triphosphate (ATP). Most importantly, the purified NudJ does not cleave the product PAPS. The removal of ADP makes the PAPS peak more separable from other components in the chromatographic purification process. This developed enzymatic approach of PAPS production will contribute to the chemoenzymatic synthesis of heparin. 
540 |a Springer-Verlag Berlin Heidelberg, 2015 
690 7 |a PAPS  |2 nationallicence 
690 7 |a ADP  |2 nationallicence 
690 7 |a Nudix hydrolase  |2 nationallicence 
690 7 |a NudJ  |2 nationallicence 
690 7 |a Heparin  |2 nationallicence 
700 1 |a Bao  |D Feifei  |u School of Biotechnology and Food Engineering, Hefei University of Technology, 230009, Hefei, China  |4 aut 
700 1 |a Yan  |D Huihui  |u School of Biotechnology and Food Engineering, Hefei University of Technology, 230009, Hefei, China  |4 aut 
700 1 |a Sun  |D Hanju  |u School of Biotechnology and Food Engineering, Hefei University of Technology, 230009, Hefei, China  |4 aut 
700 1 |a Yang  |D Peizhou  |u School of Biotechnology and Food Engineering, Hefei University of Technology, 230009, Hefei, China  |4 aut 
700 1 |a Liu  |D Guoqing  |u School of Biotechnology and Food Engineering, Hefei University of Technology, 230009, Hefei, China  |4 aut 
700 1 |a Zhou  |D Xianxuan  |u School of Biotechnology and Food Engineering, Hefei University of Technology, 230009, Hefei, China  |4 aut 
773 0 |t Applied Microbiology and Biotechnology  |d Springer Berlin Heidelberg  |g 99/24(2015-12-01), 10771-10778  |x 0175-7598  |q 99:24<10771  |1 2015  |2 99  |o 253 
856 4 0 |u https://doi.org/10.1007/s00253-015-6911-8  |q text/html  |z Onlinezugriff via DOI 
898 |a BK010053  |b XK010053  |c XK010000 
900 7 |a Metadata rights reserved  |b Springer special CC-BY-NC licence  |2 nationallicence 
908 |D 1  |a research-article  |2 jats 
949 |B NATIONALLICENCE  |F NATIONALLICENCE  |b NL-springer 
950 |B NATIONALLICENCE  |P 856  |E 40  |u https://doi.org/10.1007/s00253-015-6911-8  |q text/html  |z Onlinezugriff via DOI 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Bao  |D Feifei  |u School of Biotechnology and Food Engineering, Hefei University of Technology, 230009, Hefei, China  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Yan  |D Huihui  |u School of Biotechnology and Food Engineering, Hefei University of Technology, 230009, Hefei, China  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Sun  |D Hanju  |u School of Biotechnology and Food Engineering, Hefei University of Technology, 230009, Hefei, China  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Yang  |D Peizhou  |u School of Biotechnology and Food Engineering, Hefei University of Technology, 230009, Hefei, China  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Liu  |D Guoqing  |u School of Biotechnology and Food Engineering, Hefei University of Technology, 230009, Hefei, China  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Zhou  |D Xianxuan  |u School of Biotechnology and Food Engineering, Hefei University of Technology, 230009, Hefei, China  |4 aut 
950 |B NATIONALLICENCE  |P 773  |E 0-  |t Applied Microbiology and Biotechnology  |d Springer Berlin Heidelberg  |g 99/24(2015-12-01), 10771-10778  |x 0175-7598  |q 99:24<10771  |1 2015  |2 99  |o 253