Full Text:   <3147>

Summary:  <1992>

CLC number: Q819

On-line Access: 2014-05-05

Received: 2013-11-08

Revision Accepted: 2014-03-26

Crosschecked: 2014-04-09

Cited: 5

Clicked: 6305

Citations:  Bibtex RefMan EndNote GB/T7714

-   Go to

Article info.
Open peer comments

Journal of Zhejiang University SCIENCE B 2014 Vol.15 No.5 P.491-499

http://doi.org/10.1631/jzus.B1300283


High-level soluble expression of the hemA gene from Rhodobacter capsulatus and comparative study of its enzymatic properties*


Author(s):  Jia-wei Lou, Li Zhu, Mian-bin Wu, Li-rong Yang, Jian-ping Lin, Pei-lin Cen

Affiliation(s):  . Key Laboratory of Biomass Chemical Engineering of Ministry of Education, Department of Chemical and Biological Engineering, Zhejiang University, Hangzhou 310027, China

Corresponding email(s):   wumb@zju.edu.cn

Key Words:  5-Aminolevulinic acid, Rhodobacter capsulatus , High-level expression, Enzymatic properties


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.

荚膜红细菌hemA基因的高效可溶表达及其酶学性质对比研究

研究目的:提供一种酶学性质优良的,可在大肠杆菌体内高活性可溶表达的,具有工业应用前景的5-氨基乙酰丙酸合成酶。
创新要点:利用E. coli Rosetta (DE3)表达编码荚膜红细菌5-氨基乙酰丙酸合成酶(RC-ALAS)的hemA基因,实现其在大肠杆菌体内高活性可溶表达。以放射形土壤杆菌和类球红细菌hemA基因表达的5-氨基乙酰丙酸合成酶(AR-ALAS和RS-ALAS)为参照,对分离纯化后的RC-ALAS进行酶学性质对比研究。
研究方法:工程菌的构建如图1所示,酶的分离纯化采用镍柱亲和层析和凝胶过滤层析,酶学性质的测定采用对比研究法。
重要结论:(1)RC-ALAS酶活性高达198.2 U/mg,比AR-ALAS(151.1 U/mg)和RS-ALAS(116.9 U/mg)分别提高31.2%和69.5%;(2)RC-ALAS对底物琥珀酰辅酶A的专一性常数((kcat/Km)S-CoA)为1.4989,高于AR-ALAS(0.7456)和RS-ALAS(1.1699),具有较高的催化效率;(3)对含有荚膜红细菌hemA基因的工程菌进行补料分批发酵,发酵结束时,ALA的产量高达8.8 g/L(67 mmol/L)。

关键词:5-氨基乙酰丙酸;荚膜红细菌(Rhodobacter capsulatus);高效表达;酶学性质

Darkslateblue:Affiliate; Royal Blue:Author; Turquoise:Article

References

[1] Berkovitch, G., Doron, D., Nudelman, A., 2008. Novel multifunctional acyloxyalkyl ester prodrugs of 5-aminolevulinic acid display improved anticancer activity independent and dependent on photoactivation. J Med Chem, 51(23):7356-7369. 


[2] Bolt, E.L., Kryszak, L., Zeilstra-Ryalls, J., 1999. Characterization of the Rhodobacter sphaeroides 5-aminolaevulinic acid synthase isoenzymes, HemA and HemT, isolated from recombinant Escherichia coliEur J Biochem, 265(1):290-299. 


[3] Braathen, L.R., Szeimies, R.M., Basset-Seguin, N., 2007. Guidelines on the use of photodynamic therapy for nonmelanoma skin cancer: an international consensus. International Society for Photodynamic Therapy in Dermatology, 2005. J Am Acad Dermatol, 56(1):125-143. 


[4] Burnham, B.F., 1970. δ-Aminolevulinic acid synthase (from Rhodopseudomonas sphaeroides).  Methods in Enzymology, Volume 17, Metabolism of Amino Acids and Amines, Part A. Academic Press,USA :195-200. 


[5] Choi, C., Hong, B.S., Sung, H.C., 1999. Optimization of extracellular 5-aminolevulinic acid production from Escherichia coli transformed with ALA synthase gene of Bradyrhizobium japonicumBiotechnol Lett, 21(6):551-554. 


[6] Choi, H.P., Hong, J.W., Rhee, K.H., 2004. Cloning, expression, and characterization of 5-aminolevulinic acid synthase from Rhodopseudomonas palustris KUGB306. FEMS Microbiol Lett, 236(2):175-181. 


[7] Choi, H.P., Lee, Y.M., Yun, C.W., 2008. Extracellular 5-aminolevulinic acid production by Escherichia coli containing the Rhodopseudomonas palustris KUGB306 hemA gene. J Microbiol Biotechnol, 18(6):1136-1140. 


[8] Fan, L., 2006.  Study on Analysis and Stability of 5-Aminolevulinic Acid. MS Thesis, Zhejiang University,Hangzhou, China :

[9] Fu, W.Q., Lin, J.P., Cen, P.L., 2007. 5-Aminolevulinate production with recombinant Escherichia coli using a rare codon optimizer host strain. Appl Microbiol Biotechnol, 75(4):777-782. 


[10] Fu, W.Q., Lin, H.P., Cen, P.L., 2008. Enhancement of 5-aminolevulinate production with recombinant Escherichia coli using batch and fed-batch culture system. Bioresource Technol, 99(11):4864-4870. 


[11] Fu, W.Q., Lin, J.P., Cen, P.L., 2010. Expression of a hemA gene from Agrobacterium radiobacter in a rare codon optimizing Escherichia coli for improving 5-aminolevulinate production. Appl Microbiol Biotechnol, 160(2):456-466. 

[12] Kang, D.K., Kim, S.S., Chi, W.J., 2004. Cloning and expression of the Rhodobacter capsulatus hemA gene in E. coli for the production of 5-aminolevulinic acid. J Microbiol Biotechnol, 14(6):1327-1332. 

[13] Kiatpapan, P., Murooka, Y., 2001. Construction of an expression vector for propionibacteria and its use in production of 5-aminolevulinic acid by Propionibacterium freudenreichiiAppl Microbiol Biotechnol, 56(1-2):144-149. 


[14] Lang, K., Lehmann, P., Bolsen, K., 2001. Aminolevulinic acid: pharmacological profile and clinical indication. Expert Opin Investig Drugs, 10(6):1139-1156. 


[15] Lee, D.H., Jun, W.J., Yoon, J.W., 2004. Process strategies to enhance the production of 5-aminolevulinic acid with recombinant E. coliJ Microbiol Biotechnol, 14(6):1310-1317. 

[16] Lin, J.P., Fu, W.Q., Cen, P.L., 2009. Characterization of 5-aminolevulinate synthase from Agrobacterium radiobacter, screening new inhibitors for 5-aminolevulinate dehydratase from Escherichia coli and their potential use for high 5-aminolevulinate production. Bioresource Technol, 100(7):2293-2297. 


[17] Liu, X.X., Lin, J.P., Qin, G., 2005. Expression of a new hemA gene from Agrobacterium radiobacter in Escherichia coli for 5-aminolevulinate production. Chin J Chem Eng, 13(4):522-528. 

[18] Pariser, D., Loss, R., Jarratt, M., 2008. Topical methyl-aminolevulinate photodynamic therapy using red light-emitting diode light for treatment of multiple actinic keratoses: a randomized, double-blind, placebo-controlled study. J Am Acad Dermatol, 59(4):569-576. 


[19] Sasaki, K., Watanabe, M., Tanaka, T., 2002. Biosynthesis, biotechnological production and applications of 5-aminolevulinic acid. Appl Microbiol Biotechnol, 58(1):23-29. 


[20] Vanderwerf, M.J., Zeikus, J.G., 1996. 5-Aminolevulinate production by Escherichia coli containing the Rhodobacter sphaeroides hemA gene. Appl Environ Microbiol, 62(10):3560-3566. 


[21] Viale, A.A., Wider, E.A., Batlle, A.M.D.C., 1987. Porphyrin biosynthesis in Rhodopseudomonas palustris—XI. Extraction and characterization of δ-aminolevulinate synthetase. Comp Biochem Physiol B Comp Biochem, 87(3):607-613. 


[22] Wang, J.Q., Wu, J.H., Zhang, Z.M., 2006. Expression of 5-aminolevulinic acid synthase in recombinant Escherichia coliWorld J Microbiol Biotechnol, 22(5):461-468. 


[23] Warnick, G.R., Burnham, B.F., 1971. Regulation of porphyrin biosynthesis. Purification and characterization of δ-aminolevulinic acid synthase. J Biol Chem, 246(22):6880-6885. 


[24] Xie, L., Hall, D., Eiteman, M.A., 2003. Optimization of recombinant aminolevulinate synthase production in Escherichia coli using factorial design. Appl Microbiol Biotechnol, 63(3):267-273. 


[25] Xie, L., Eiteman, M.A., Altman, E., 2003. Production of 5-aminolevulinic acid by an Escherichia coli aminolevulinate dehydratase mutant that overproduces Rhodobacter sphaeroides aminolevulinate synthase. Biotechnol Lett, 25(20):1751-1755. 


[26] Zaak, D., Sroka, R., Khoder, W., 2008. Photodynamic diagnosis of prostate cancer using 5-aminolevulinic acid: first clinical experiences. Urology, 72(2):345-348. 



Open peer comments: Debate/Discuss/Question/Opinion

<1>

Please provide your name, email address and a comment





Journal of Zhejiang University-SCIENCE, 38 Zheda Road, Hangzhou 310027, China
Tel: +86-571-87952783; E-mail: cjzhang@zju.edu.cn
Copyright © 2000 - 2024 Journal of Zhejiang University-SCIENCE