Identification of transporter proteins for PQQ-secretion pathways by transcriptomics and proteomics analysis in Gluconobacter oxydans WSH-003

Hui Wan, Yu Xia, Jianghua Li, Zhen Kang, Jingwen Zhou

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Front. Chem. Sci. Eng. ›› 2017, Vol. 11 ›› Issue (1) : 72-88. DOI: 10.1007/s11705-016-1580-4
RESEARCH ARTICLE

Identification of transporter proteins for PQQ-secretion pathways by transcriptomics and proteomics analysis in Gluconobacter oxydans WSH-003

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Abstract

Pyrroloquinoline quinone (PQQ) plays a significant role as a redox cofactor in combination with dehydrogenases in bacteria. These dehydrogenases play key roles in the oxidation of important substrates for the biotechnology industry, such as vitamin C production. While biosynthesis of PQQ genes has been widely studied, PQQ-transport mechanisms remain unclear. Herein, we used both two-dimensional fluorescence-difference gel electrophoresis tandem mass spectrometry and RNA sequencing to investigate the effects of pqqB overexpression in an industrial strain of Gluconobacter oxydans WSH-003. We have identified 73 differentially expressed proteins and 99 differentially expressed genes, a majority of which are related to oxidation-reduction and transport processes by gene ontology analysis. We also described several putative candidate effectors that responded to increased PQQ levels resulting from pqqB overexpression. Furthermore, quantitative PCR was used to verify five putative PQQ-transport genes among different PQQ producing strains, and the results showed that ompW, B932_1930 and B932_2186 were upregulated in all conditions. Then the three genes were over-expressed in G. oxydans WSH-003 and PQQ production were detected. The results showed that extracellular PQQ of B932_1930 (a transporter) and B932_2186 (an ABC transporter permease) overexpression strains were enhanced by 1.77-fold and 1.67-fold, respectively. The results suggest that the proteins encoded by PqqB, B932_1930 and B932_2186 might enhance the PQQ secretion process.

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Keywords

2D-DIGE / pqqB / pyrroloquinoline quinone / RNA-Seq / Vitamin C

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Hui Wan, Yu Xia, Jianghua Li, Zhen Kang, Jingwen Zhou. Identification of transporter proteins for PQQ-secretion pathways by transcriptomics and proteomics analysis in Gluconobacter oxydans WSH-003. Front. Chem. Sci. Eng., 2017, 11(1): 72‒88 https://doi.org/10.1007/s11705-016-1580-4

References

[1]
Kasahara T, Kato T. A new redox-cofactor vitamin for mammals. Nature, 2003, 422(6934): 832
CrossRef Google scholar
[2]
Goodwin P M, Anthony C. The biochemistry, physiology and genetics of PQQ and PQQ-containing enzymes. Advances in Microbial Physiology, 1998, 40: 1–80
CrossRef Google scholar
[3]
Matsushita K, Toyama H, Adachi O. Respiratory chains and bioenergetics of acetic-acid bacteria. Advances in Microbial Physiology, 1994, 36: 247–301
CrossRef Google scholar
[4]
Sashidhar B, Podile A R. Mineral phosphate solubilization by rhizosphere bacteria and scope for manipulation of the direct oxidation pathway involving glucose dehydrogenase. Journal of Applied Microbiology, 2010, 109(1): 1–12
[5]
Zhou Y L, Dong H, Liu L T, Hao Y Q, Chang Z, Xu M T. Fabrication of electrochemical interface based on boronic acid-modified pyrroloquinoline quinine/reduced graphene oxide composites for voltammetric determination of glycated hemoglobin. Biosensors & Bioelectronics, 2015, 64: 442–448
CrossRef Google scholar
[6]
Bauerly K, Harris C, Chowanadisai W, Graham J, Havel P J, Tchaparian E, Satre M, Karliner J S, Rucker R B. Altering pyrroloquinoline quinone nutritional status modulates mitochondrial, lipid, and energy metabolism in rats. PLoS One, 2011, 6(7): e21779
CrossRef Google scholar
[7]
Kumar N, Kar A. Pyrroloquinoline quinone ameliorates oxidative stress and lipid peroxidation in the brain of streptozotocin-induced diabetic mice. Canadian Journal of Physiology and Pharmacology, 2015, 93(1): 71–79
CrossRef Google scholar
[8]
Kimura K, Takada M, Ishii T, Tsuji-Naito K, Akagawa M. Pyrroloquinoline quinone stimulates epithelial cell proliferation by activating epidermal growth factor receptor through redox cycling. Free Radical Biology & Medicine, 2012, 53(6): 1239–1251
CrossRef Google scholar
[9]
Misra H S, Rajpurohit Y S, Khairnar N P. Pyrroloquinoline-quinone and its versatile roles in biological processes. Journal of Biosciences, 2012, 37(2): 313–325
CrossRef Google scholar
[10]
Houck D R, Hanners J L, Unkefer C J, van Kleef M A G, Duine J A. PQQ: Biosynthetic studies in Methylobacterium AM1 and Hyphomicrobium X using specific 13C labeling and NMR. Antonie van Leeuwenhoek, 1989, 56(1): 93–101
CrossRef Google scholar
[11]
Li L, Jiao Z W, Hale L, Wu W L, Guo Y B. Disruption of gene pqqA or pqqB reduces plant growth promotion activity and biocontrol of crown gall disease by Rahnella aquatilis HX2. PLoS One, 2014, 9(12): 16
[12]
Hölscher T, Görisch H. Knockout and overexpression of pyrroloquinoline quinone biosynthetic genes in Gluconobacter oxydans 621H. Journal of Bacteriology, 2006, 188(21): 7668–7676
CrossRef Google scholar
[13]
Wecksler S R, Stoll S, Iavarone A T, Imsand E M, Tran H, Britt R D, Klinman J P. Interaction of PqqE and PqqD in the pyrroloquinoline quinone (PQQ) biosynthetic pathway links PqqD to the radical SAM superfamily. Chemical Communications, 2010, 46(37): 7031–7033
CrossRef Google scholar
[14]
Yang X P, Zhong G F, Lin J P, Mao D B, Wei D Z. Pyrroloquinoline quinone biosynthesis in Escherichia coli through expression of the Gluconobacter oxydans pqqABCDE gene cluster. Journal of Industrial Microbiology & Biotechnology, 2010, 37(6): 575–580
CrossRef Google scholar
[15]
Velterop J S, Sellink E, Meulenberg J J, David S, Bulder I. Synthesis of pyrroloquinoline quinone in vivo and in vitro and detection of an intermediate in the biosynthetic pathway. Journal of Bacteriology, 1995, 177: 5088–5098
[16]
Puehringer S, Metlitzky M, Schwarzenbacher R. The pyrroloquinoline quinone biosynthesis pathway revisited: A structural approach. BMC Biochemistry, 2008, 9(1): 8
CrossRef Google scholar
[17]
Shen Y Q, Bonnot F, Imsand E M, RoseFigura J M, Sjölander K, Klinman J P. Distribution and properties of the genes encoding the biosynthesis of the bacterial cofactor, pyrroloquinoline quinone. Biochemistry, 2012, 51(11): 2265–2275
CrossRef Google scholar
[18]
Klinman J P, Bonnot F. Intrigues and intricacies of the biosynthetic pathways for the enzymatic quinocofactors: PQQ, TTQ, CTQ, TPQ, and LTQ. Chemical Reviews, 2014, 114(8): 4343–4365
CrossRef Google scholar
[19]
Gao L L, Hu Y D, Liu J, Du G C, Zhou J W, Chen J. Stepwise metabolic engineering of Gluconobacter oxydans WSH-003 for the direct production of 2-keto-L-gulonic acid from D-sorbitol. Metabolic Engineering, 2014, 24: 30–37
CrossRef Google scholar
[20]
Xu S, Wang X B, Du G C, Zhou J W, Chen J. Enhanced production of L-sorbose from D-sorbitol by improving the mRNA abundance of sorbitol dehydrogenase in Gluconobacter oxydans WSH-003. Microbial Cell Factories, 2014, 13(1): 1–7
CrossRef Google scholar
[21]
Gao L L, Zhou J W, Liu J, Du G C, Chen J. Draft genome sequence of Gluconobacter oxydans WSH-003, a strain that is extremely tolerant of saccharides and alditols. Journal of Bacteriology, 2012, 194(16): 4455–4456
CrossRef Google scholar
[22]
Zhou J W, Du G C, Chen J. Metabolic engineering of microorganisms for vitamin C production. Sub-Cellular Biochemistry, 2012, 64: 241–259
CrossRef Google scholar
[23]
Wang X B, Liu J, Du G C, Zhou J W, Chen J. Efficient production of L-sorbose from D-sorbitol by whole cell immobilization of Gluconobacter oxydans WSH-003. Biochemical Engineering Journal, 2013, 77: 171–176
CrossRef Google scholar
[24]
Hu Y D, Wan H, Li J, Zhou J W. Enhanced production of L-sorbose in an industrial Gluconobacter oxydans strain by identification of a strong promoter based on proteomics analysis. Journal of Industrial Microbiology & Biotechnology, 2015, 42(7): 1039–1047
CrossRef Google scholar
[25]
Kovach M E, Elzer P H, Hill D S, Robertson G T, Farris M A, Roop R M, Peterson K M. Four new derivatives of the broad-host-range cloning vector pBBR1MCS, carrying different antibiotic-resistance cassettes. Gene, 1995, 166(1): 175–176
CrossRef Google scholar
[26]
Zhang L, Lin J P, Ma Y S, Wei D Z, Sun M. Construction of a novel shuttle vector for use in Gluconobacter oxydans. Molecular Biotechnology, 2010, 46(3): 227–233
CrossRef Google scholar
[27]
Geiger O, Gorisch H. Enzymatic determination of pyrroloquinoline quinone using crude membranes from Escherichia coli. Analytical Biochemistry, 1987, 164(2): 418–423
CrossRef Google scholar
[28]
Rochat T, Delumeau O, Figueroa-Bossi N, Noirot P, Bossi L, Dervyn E, Bouloc P. Tracking the elusive function of Bacillus subtilis Hfq. PLoS One, 2015, 10(4): e0124977
CrossRef Google scholar
[29]
Trapnell C, Roberts A, Goff L, Pertea G, Kim D, Kelley D R, Pimentel H, Salzberg S L, Rinn J L, Pachter L. Differential gene and transcript expression analysis of RNA-seq experiments with TopHat and Cufflinks. Nature Protocols, 2012, 7(3): 562–578
CrossRef Google scholar
[30]
Zhou J W, Wang K, Xu S, Wu J J, Liu P R, Du G C, Li J H, Chen J. Identification of membrane proteins associated with phenylpropanoid tolerance and transport in Escherichia coli BL21. Journal of Proteomics, 2015, 113: 15–28
CrossRef Google scholar
[31]
Huang C Z, Lin X M, Wu L N, Zhang D F, Liu D, Wang S Y, Peng X X. Systematic identification of the subproteome of Escherichia coli cell envelope reveals the interaction network of membrane proteins and membrane-associated peripheral proteins. Journal of Proteome Research, 2006, 5(12): 3268–3276
CrossRef Google scholar
[32]
Wu C D, Zhang J, Chen W, Wang M, Du G C, Chen J. A combined physiological and proteomic approach to reveal lactic-acid-induced alterations in Lactobacillus casei Zhang and its mutant with enhanced lactic acid tolerance. Applied Microbiology and Biotechnology, 2012, 93(2): 707–722
CrossRef Google scholar
[33]
Götz S, García-Gómez J M, Terol J, Williams T D, Nagaraj S H, Nueda M J, Robles M, Talon M, Dopazo J, Conesa A. High-throughput functional annotation and data mining with the Blast2GO suite. Nucleic Acids Research, 2008, 36(10): 3420–3435
CrossRef Google scholar
[34]
Yu N Y, Wagner J R, Laird M R, Melli G, Rey S, Lo R, Dao P, Sahinalp S C, Ester M, Foster L J, Brinkman F S L. PSORTb 3.0: Improved protein subcellular localization prediction with refined localization subcategories and predictive capabilities for all prokaryotes. Bioinformatics (Oxford, England), 2010, 26(13): 1608–1615
CrossRef Google scholar
[35]
Zhao S H, Zhao X R, Zou H J, Fu J W, Du G C, Zhou J W, Chen J. Comparative proteomic analysis of Saccharomyces cerevisiae under different nitrogen sources. Journal of Proteomics, 2014, 101: 102–112
CrossRef Google scholar
[36]
Hölscher T, Schleyer U, Merfort M, Bringer-Meyer S, Görisch H, Sahm H. Glucose oxidation and PQQ-dependent dehydrogenases in Gluconobacter oxydans. Journal of Molecular Microbiology and Biotechnology, 2009, 16(1-2): 6–13
CrossRef Google scholar
[37]
Klein G, Dartigalongue C, Raina S. Phosphorylation-mediated regulation of heat shock response in Escherichia coli. Molecular Microbiology, 2003, 48(1): 269–285
CrossRef Google scholar
[38]
Frydman J. Folding of newly translated proteins in vivo: the role of molecular chaperones. Annual Review of Biochemistry, 2001, 70(1): 603–647
CrossRef Google scholar
[39]
Mogk A, Schlieker C, Friedrich K L, Schönfeld H J, Vierling E, Bukau B. Refolding of substrates bound to small Hsps relies on a disaggregation reaction mediated most efficiently by ClpB/DnaK. Journal of Biological Chemistry, 2003, 278(33): 31033–31042
CrossRef Google scholar
[40]
Nakamoto H, Vigh L. The small heat shock proteins and their clients. Cellular and Molecular Life Sciences, 2007, 64(3): 294–306
CrossRef Google scholar
[41]
Ameyama M, Matsushita K, Ohno Y, Shinagawa E, Adachi O. Existence of a novel prosthetic group, PQQ, in membrane-bound, electron transport chain-linked, primary dehydrogenases of oxidative bacteria. FEBS Letters, 1981, 130(2): 179–183
CrossRef Google scholar
[42]
Schobert M, Gorisch H. Cytochrome c550 is an essential component of the quinoprotein ethanol oxidation system in Pseudomonas aeruginosa: Cloning and sequencing of the genes encoding cytochrome c550 and an adjacent acetaldehyde dehydrogenase. Microbiology, 1999, 145(2): 471–481
CrossRef Google scholar
[43]
Peters C, Koelzsch R, Kadow M, Skalden L, Rudroff F, Mihovilovic M D, Bornscheuer U T. Identification, characterization, and application of three enoate reductases from pseudomonas putida in in vitro enzyme cascade reactions. ChemCatChem, 2014, 6(4): 1021–1027
CrossRef Google scholar
[44]
Prust C, Hoffmeister M, Liesegang H, Wiezer A, Fricke W F, Ehrenreich A, Gottschalk G, Deppenmeier U. Complete genome sequence of the acetic acid bacterium Gluconobacter oxydans. Nature Biotechnology, 2005, 23(2): 195–200
CrossRef Google scholar
[45]
Nachin L, Loiseau L, Expert D, Barras F, Suf C. An unorthodox cytoplasmic ABC/ATPase required for Fe-S biogenesis under oxidative stress. EMBO Journal, 2003, 22(3): 427–437
CrossRef Google scholar
[46]
Romao C V, Ladakis D, Lobo S A L, Carrondo M A, Brindley A A, Deery E, Matias P M, Pickersgill R W, Saraiva L M, Warren M J. Evolution in a family of chelatases facilitated by the introduction of active site asymmetry and protein oligomerization. Proceedings of the National Academy of Sciences of the United States of America, 2011, 108(1): 97–102
CrossRef Google scholar
[47]
Merlin C, Gardiner G, Durand S, Masters M. The Escherichia coli metD locus encodes an ABC transporter which includes Abc (MetN), YaeE (MetI), and YaeC (MetQ). Journal of Bacteriology, 2002, 184(19): 5513–5517
CrossRef Google scholar
[48]
Albrecht R, Zeth K, Söding J, Lupas A, Linke D. Expression, crystallization and preliminary X-ray crystallographic studies of the outer membrane protein OmpW from Escherichia coli. Acta Crystallographica. Section F, Structural Biology and Crystallization Communications, 2006, 62(4): 415–418
CrossRef Google scholar
[49]
Sun D C, Wang B, Zhu L H, Chen M Y, Zhan L L. Block and boost DNA transfer: Opposite roles of OmpA in natural and artificial transformation of Escherichia coli. PLoS One, 2013, 8(3): 8
CrossRef Google scholar

Acknowledgements

This work was supported by grants from the National High Technology Research and Development Program of China (863 Program, 2012AA022103), the National Basic Research Program of China (973 Program, 2013CB733602, 2014CB745100), the Major Program of National Natural Science Foundation of China (Grant No. 21390204), the Program for New Century Excellent Talents in University (NCET-12-0876), the Foundation for the Author of National Excellent Doctoral Dissertation of China (FANEDD, 201256), the Priority Academic Program Development of Jiangsu Higher Education Institutions, and the 111 Project (111-2-06).

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2017 Higher Education Press and Springer-Verlag Berlin Heidelberg
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