Cultural optimization and metal effects of Shewanella xiamenensis BC01 growth and swarming motility

I-Son Ng, Chukwuma Isaac Ndive, Yunli Zhou, Xiaomin Wu

Bioresources and Bioprocessing ›› 2015, Vol. 2 ›› Issue (1) : 28.

Bioresources and Bioprocessing All Journals
Bioresources and Bioprocessing ›› 2015, Vol. 2 ›› Issue (1) : 28. DOI: 10.1186/s40643-015-0055-7
Research

Cultural optimization and metal effects of Shewanella xiamenensis BC01 growth and swarming motility

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Abstract

Background

Shewanella species belonging to dissimilatory metal bacteria were found to decolorize most textile dyes and had also attracted great interests in regard to bioremediation. However, studies have rarely been reported on Shewanella xiamenensis BC01, which was isolated as a biodecolorization and bioelectricity strain recently. In this study, the effect of cultivation conditions on S. xiamenensis BC01 was studied to explore how environmental conditions may influence S. xiamenensis growth and swarming motility.

Results

Shewanella xiamenensis BC01 grew over a wide range of pH (5.0–9.0) and mild temperatures (25–42 °C). The optimal conditions for cell growth were using Luria-Bertani (LB) as medium with shaking at 150 rpm, 37 °C, and pH 8.0 which had been confirmed by shift pH and temperature. S. xiamenensis BC01 was able to resist 1 mM concentrations of various metal ions, i.e., Ca2+, Mg2+, Cu2+, Zn2+, Mn2+, Fe3+, and Al3+, respectively. As shown in scanning electron microscopy (SEM) analyses, cell morphologies were slightly changed under metal stress. Swarming motility showed that the velocity ranking at 80 μM and 1 mM of metal was Al > Cr > LB > Zn > Fe > Cu and Mg > Mn > Ca, respectively.

Conclusions

This study evaluates the impact of cultivation methods and metal ions on the activity of S. xiamenensis BC01 and provides an alternative to bioremediation of heavy metal-containing wastewaters by utilizing this strain.

Keywords

Shewanella xiamenensis / Optimization / Heavy metal / Swarming motility

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I-Son Ng, Chukwuma Isaac Ndive, Yunli Zhou, Xiaomin Wu. Cultural optimization and metal effects of Shewanella xiamenensis BC01 growth and swarming motility. Bioresources and Bioprocessing, 2015, 2(1): 28 https://doi.org/10.1186/s40643-015-0055-7

References

[1.]
Bruins MR, Kapil S, Oehme FW. Microbial resistance to metals in the environment. Ecotox Environ Safe, 2000, 45(3): 198-207.
CrossRef Google scholar
[2.]
Gadd GM. Microbial influence on metal mobility and application for bioremediation. Geoderma, 2004, 122: 109-119.
CrossRef Google scholar
[3.]
Lovley DR. Dissimilatory metal reduction. Annu Rev Microbiol, 1993, 47: 263-290.
CrossRef Google scholar
[4.]
Gorby YA, Lovley DR. Enzymic uranium precipitation. Environ Sci Technol, 1992, 26(1): 205-207.
CrossRef Google scholar
[5.]
Gorby YA, Caccavo F, Bolton H. Microbial reduction of cobalt III EDTA- in the presence and absence of manganese(IV) oxide. Environ Sci Technol, 1998, 32(2): 244-250.
CrossRef Google scholar
[6.]
Liu C, Gorby YA, Zachara JM, Fredrickson JK, Brown CF. Reduction kinetics of Fe(III), Co(III), U(VI), Cr(VI), and Tc(VII) in cultures of dissimilatory metal-reducing bacteria. Biotechnol Bioeng, 2002, 80(6): 637-649.
CrossRef Google scholar
[7.]
Nealson KH, Saffarini D. Iron and manganese in anaerobic respiration: environmental significance, physiology, and regulation. Annu Rev Microbiol, 1994, 48: 311-343.
CrossRef Google scholar
[8.]
Wildung RE, Gorby YA, Krupka KM, Hess NJ, Li SW, Plymale AE. Effect of electron donor and solution chemistry on products of dissimilatory reduction of technetium by Shewanella putrefaciens. Appl Environ Microbiol, 2000, 66(6): 2451-2460.
CrossRef Google scholar
[9.]
Liu SV, Zhou J, Zhang C, Cole DR, Gajdarziska-Josifovska M, Phelps TJ. Thermophilic Fe(III)-reducing bacteria from the deep subsurface: the evolutionary implications. Science, 1997, 277(5329): 1106-1109.
CrossRef Google scholar
[10.]
Roh Y, Liu SV, Li G, Huang H, Phelps TJ, Zhou J. Isolation and characterization of metal-reducing thermoanaerobacter strains from deep subsurface environments of the Piceance Basin, Colorado. Appl Environ Microbiol, 2002, 68(12): 6013-20.
CrossRef Google scholar
[11.]
Fredrickson JK, Zachara JM, Kennedy DW, Dong H, Onstott TC, Hinman NW, Li S. Biogenic iron mineralization accompanying the dissimilatory reduction of hydrous ferric oxide by a groundwater bacterium. Geochim Cosmochim Ac, 1998, 62: 3239-3257.
CrossRef Google scholar
[12.]
Roh Y, Gao H, Vali H, Kennedy DW, Yang ZK, Gao W, Dohnalkova AC, Stapleton RD, Moon JW, Phelps TJ, Fredrickson JK, Zhou J. Metal reduction and iron biomineralization by a psychrotolerant Fe(III)-reducing bacterium, Shewanella sp. strain PV-4. Appl Environ Microb, 2006, 72(5): 3236-3244.
CrossRef Google scholar
[13.]
Ahluwalia SS, Goyal D. Microbial and plant derived biomass for removal of heavy metals from wastewater. Bioresour Technol, 2007, 98: 2243-2257.
CrossRef Google scholar
[14.]
Babel S, Kurniawan TA. Low-cost adsorbent for heavy metal uptake from contaminated water a review. J Hazard Mater, 2003, 397: 219-243.
CrossRef Google scholar
[15.]
Ng IS, Chen T, Lin R, Zhang X, Ni C, Sun D. Decolorization of textile azo dye and Congo red by an isolated strain of the dissimilatory manganese-reducing bacterium Shewanella xiamenensis BC01. Appl Microbiol Biotechnol, 2014, 98(5): 2297-2308.
CrossRef Google scholar
[16.]
Venil CK, Mohan V, Lakshmanaperumalsamy P, Yerima MB. Optimization of chromium removal by the indigenous bacterium Bacillus spp. REP02 using the response surface methodology, 2011 951694.
[17.]
Lovley DR, Holmes DE, Nevin KP. Dissimilatory Fe(III) and Mn(IV) reduction. Adv Microbiol Physiol, 2004, 49: 219-286.
CrossRef Google scholar
[18.]
MacDonell MT, Colwell RR. Phylogeny of the Vibrionaceae, and recommendation for two new genera, Listonella and Shewanella. Syst Appl Microbiol, 1985, 6: 171-182.
CrossRef Google scholar
[19.]
Venkateswaran K, Moser D, Dollhopf M, Lies D, Saffarini D, MacGregor B, Ringelberg D, White D, Nishijima M, Sano H, Burghardt J, Stackebrandt E, Nealson KH. Polyphasic taxonomy of the genus Shewanella and description of Shewanella oneidensis sp. nov. Int J Syst Bacteriol, 1999, 49: 705-724.
CrossRef Google scholar
[20.]
Nealson KH, Scott J. Ecophysiology of the genus Shewanella. In the Prokaryotes: a Handbook on the Biology of Bacteria, 2006, 6: 1133-1151.
CrossRef Google scholar
[21.]
Hau HH, Gralnick JA. Ecology and biotechnology of the genus Shewanella. Annu Rev Microbiol, 2007, 61(1): 237-258.
CrossRef Google scholar
[22.]
Huang J, Sun B, Zhang X. Shewanella xiamenensis sp. nov., isolated from coastal sea sediment. Int J Syst Evol Microbiol, 2010, 60: 1585-1589.
CrossRef Google scholar
[23.]
Jian H, Xiao X, Wang F. Role of filamentous phage SW1 in regulating the lateral flagella of Shewanella piezotolerans strain WP3 at low temperatures. Appl Environ Microbiol, 2013, 79(22): 7101-7109.
CrossRef Google scholar
[24.]
Burkart M, Toguchi A, Harshey RM. The chemotaxis system, but not chemotaxis, is essential for swarming motility in Escherichia coli. Proc Natl Acad Sci USA, 1998, 95(5): 2568-2573.
CrossRef Google scholar
[25.]
Middleton S, Latmani R, Mackey M, Ellisman M, Tebo B, Criddle C. Cometabolism of Cr(VI) by Shewanella oneidensis MR-1 produces cell-associated reduced chromium and inhibits growth. Biotechnol Bioeng, 2003, 83: 627-637.
CrossRef Google scholar
[26.]
Elias DA, Tollaksen SL, Kennedy DW, Mottaz HM, Giometti CS, McLean JS, Hill EA, Pinchuk GE, Lipton MS, Fredrickson JK, Gorby YA. The influence of cultivation methods on Shewanella oneidensis physiology and proteome expression. Arch Microbiol, 2008, 189(4): 313-324.
CrossRef Google scholar
[27.]
Hardoyo JK, Ohtake H. Effects of heavy metal cations on chromate reduction by Enterobacter cloacae strain HO1. J Gen Appl Microbiol, 1991, 37: 519-522.
CrossRef Google scholar
[28.]
Wang H, Law N, Pearson G, van Dongen BE, Jarvis RM, Goodacre R, Lloyd JR. Impact of silver(I) on the metabolism of Shewanella oneidensis. J Bacteriol, 2010, 192(4): 1143-1150.
CrossRef Google scholar
[29.]
El-Naggar MY, Wanger G, Leung KM, Yuzvinsky TD, Southam G, Yang J, Lau M, Nealson KH, Gorby YA. Electrical transport along bacterial nanowires from Shewanella oneidensis MR-1. Proc Natl Acad Sci USA, 2010, 107: 18127-18131.
CrossRef Google scholar
[30.]
Gorby YA, Yanina S, Mclean JS, Rosso KM, Moyles D, Dohnalkova A, Beveridge TJ, Chang IS, Kim BH, Kim KS, Culley DE, Reed SB, Romine MF, Saffarini DA, Hill EA, Shi L, Elias DA, Kennedy DW, Pinchuk G, Watanabe K, Ishii S, Logan B, Nealson KH, Fredrickson JK. Electrically conductive bacterial nanowires produced by Shewanella oneidensis strain MR-1 and other microorganisms. Proc Natl Acad Sci USA, 2006, 103(30): 11358-11363.
CrossRef Google scholar
[31.]
Fraser GM, Hughes C. Swarming motility. Curr Opin Microbiol, 1999, 2: 630-635.
CrossRef Google scholar
[32.]
Paulick A, Koerdt A, Lassak J, Huntley S, Wilms I, Narberhaus F, Thormann KM. Two different stator systems drive a single polar flagellum in Shewanella oneidensis MR-1. Mol Microbiol, 2009, 71(4): 836-850.
CrossRef Google scholar
[33.]
Inoue T, Shingaki R, Fukui K. Inhibition of swarming motility of Pseudomonas aeruginosa by branched-chain fatty acids. FEMS Microbiol Lett, 2008, 281(1): 81-86.
CrossRef Google scholar
[34.]
Harshey RM. Bacterial motility on a surface: many ways to a common goal. Annu Rev Microbiol, 2003, 57: 249-273.
CrossRef Google scholar
Funding
National Natural Science Foundation of China(21206142); National High-Tech R&D Program of China(2014AA021701); Ministry of Science and Technology, Taiwan(MOST 103-2218-E-006-027-MY2)

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