CLC number: Q819
On-line Access: 2024-08-27
Received: 2023-10-17
Revision Accepted: 2024-05-08
Crosschecked: 2014-04-09
Cited: 5
Clicked: 7187
Jia-wei Lou, Li Zhu, Mian-bin Wu, Li-rong Yang, Jian-ping Lin, Pei-lin Cen. High-level soluble expression of the hemA gene from Rhodobacter capsulatus and comparative study of its enzymatic properties[J]. Journal of Zhejiang University Science B, 2014, 15(5): 491-499.
@article{title="High-level soluble expression of the hemA gene from Rhodobacter capsulatus and comparative study of its enzymatic properties",
author="Jia-wei Lou, Li Zhu, Mian-bin Wu, Li-rong Yang, Jian-ping Lin, Pei-lin Cen",
journal="Journal of Zhejiang University Science B",
volume="15",
number="5",
pages="491-499",
year="2014",
publisher="Zhejiang University Press & Springer",
doi="10.1631/jzus.B1300283"
}
%0 Journal Article
%T High-level soluble expression of the hemA gene from Rhodobacter capsulatus and comparative study of its enzymatic properties
%A Jia-wei Lou
%A Li Zhu
%A Mian-bin Wu
%A Li-rong Yang
%A Jian-ping Lin
%A Pei-lin Cen
%J Journal of Zhejiang University SCIENCE B
%V 15
%N 5
%P 491-499
%@ 1673-1581
%D 2014
%I Zhejiang University Press & Springer
%DOI 10.1631/jzus.B1300283
TY - JOUR
T1 - High-level soluble expression of the hemA gene from Rhodobacter capsulatus and comparative study of its enzymatic properties
A1 - Jia-wei Lou
A1 - Li Zhu
A1 - Mian-bin Wu
A1 - Li-rong Yang
A1 - Jian-ping Lin
A1 - Pei-lin Cen
J0 - Journal of Zhejiang University Science B
VL - 15
IS - 5
SP - 491
EP - 499
%@ 1673-1581
Y1 - 2014
PB - Zhejiang University Press & Springer
ER -
DOI - 10.1631/jzus.B1300283
Abstract: The Rhodobacter capsulatus hemA gene, which encodes 5-Aminolevulinic acid synthase (ALAS), was expressed in Escherichia coli Rosetta (DE3) and the enzymatic properties of the purified recombinant ALAS (RC-ALAS) were studied. Compared with ALASs encoded by hemA genes from Agrobacterium radiobacter (AR-ALAS) and Rhodobacter sphaeroides (RS-ALAS), the specific activity of RC-ALAS reached 198.2 U/mg, which was about 31.2% and 69.5% higher than those of AR-ALAS (151.1 U/mg) and RS-ALAS (116.9 U/mg), respectively. The optimum pH values and temperatures of the three above mentioned enzymes were all pH 7.5 and 37 °C, respectively. Moreover, RC-ALAS was more sensitive to pH, while the other two were sensitive to temperature. The effects of metals, ethylene diamine tetraacetic acid (EDTA), and sodium dodecyl sulfate (SDS) on the three ALASs were also investigated. The results indicate that they had the same effects on the activities of the three ALASs. SDS and metal ions such as Co2+, Zn2+, and Cu2+ strongly inhibited the activities of the ALASs, while Mn2+ exerted slight inhibition, and K+, Ca2+, Ba2+, Mg2+, or EDTA had no significant effect. The specificity constant of succinyl coenzyme A [(k
cat/K
m)S-CoA] of RC-ALAS was 1.4989, which was higher than those of AR-ALAS (0.7456) and RS-ALAS (1.1699), showing its high catalytic efficiency. The fed-batch fermentation was conducted using the recombinant strain containing the R. capsulatus hemA gene, and the yield of 5-Aminolevulinic acid (ALA) achieved was 8.8 g/L (67 mmol/L) under the appropriate conditions.
Open peer comments: Debate/Discuss/Question/Opinion
<1>