Accepted Manuscript
Biological filters and their use in potable water filtration systems in spaceflight conditions Starla G. Thornhill , Manish Kumar PII: DOI: Reference:
S2214-5524(17)30105-0 10.1016/j.lssr.2018.03.003 LSSR 169
To appear in:
Life Sciences in Space Research
Received date: Revised date: Accepted date:
14 October 2017 16 February 2018 4 March 2018
Please cite this article as: Starla G. Thornhill , Manish Kumar , Biological filters and their use in potable water filtration systems in spaceflight conditions, Life Sciences in Space Research (2018), doi: 10.1016/j.lssr.2018.03.003
This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to our customers we are providing this early version of the manuscript. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final form. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain.
ACCEPTED MANUSCRIPT
Biological filters and their use in potable water filtration systems in spaceflight conditions
CR IP T
Starla G. Thornhill and Manish Kumar* Department of Biology, Texas State university, San Marcos, Texas -78666, USA Starla G. Thornhill email:
[email protected] *Corresponding author
AN US
Dr. Manish Kumar Tel: 1-512-245-8968 Fax: 1-512-245-8713
AC
CE
PT
ED
M
Email:
[email protected]
1
ACCEPTED MANUSCRIPT
Abstract Providing drinking water to space missions such as the International Space
CR IP T
Station (ISS) is a costly requirement for human habitation. To limit the costs of water transport, wastewater is collected and purified using a variety of physical and chemical means. To date, sand-based biofilters have been designed to
function against gravity, and biofilms have been shown to form in microgravity
AN US
conditions. Development of a universal silver-recycling biological filter system that is able to function in both microgravity and full gravity conditions would
reduce the costs incurred in removing organic contaminants from wastewater by limiting the energy and chemical inputs required. This paper aims to propose the
on manned spaceflights.
M
use of a sand-substrate biofilter to replace chemical means of water purification
ED
Keywords: Biofilters, microgravity, manned space flight, life support systems,
PT
biological filters, water filtration systems
CE
Abbreviations EPS: extracellular polymeric matrix, GAC: granular activated charcoal, OM: organic material, PVP: polyvinylpyrrolidone, AgNP: silver
AC
nanoparticles, LSMMG: low shear modeled microgravity, RWV: rotating wall vessel, HARV: high aspect ratio vessel
2
ACCEPTED MANUSCRIPT
1. Introduction On manned space missions such as the International Space Station (ISS),
CR IP T
transportation of materials, including drinking water, is prohibitively costly at approximately $10,000 per pound of payload (Jones, 2015). To limit transport costs for water delivery, wastewater in the form of sewage waste and ambient
humidity, caused by astronaut sweat and breath, is collected and purified to serve
AN US
as drinking water (Shaw and Barreda, 2008). There are two water filtration systems on ISS. The Russian Potable Water Dispenser (PWD) (Figure 1)
equipped on the Zvezda module provides support for a crew of three and serves as the backup filtration system (Shaw and Barreda, 2008). The American
M
Environmental Control and Life Support System (ECLSS), equipped on the Tranquility module provides drinking support for six crew members (Shaw and
ED
Barreda, 2008). Both systems function by utilizing chemical and physical
PT
methods of treatment (Carrasquillo, 2005). Chemical methods include iodine sterilization (Wong et al., 2010), ion exchange chromatography, and catalytic
CE
oxidation (Carrasquillo, 2005), while physical methods include removal of
AC
microorganisms using 0.2 micron filters (Wong et al., 2010). Though the current methods are generally effective at wastewater clean-up
(Wong et al., 2010; Pierson et al., 2012), supplies must be replenished periodically to continuously provide a supply of clean drinking water to the crew in residence. At the cost of $10,000 per pound, transport of treatment chemicals
3
ACCEPTED MANUSCRIPT
and filters is costly. A larger crew could be supported by providing an additional water filtration system which would incur increased costs in transportation of
CR IP T
chemical treatments and replacement filters. In addition to the significant financial requirements for water treatment, iodine as a sterilization method poses a health risk to potential astronauts as a causative agent for hyperthyroidism and
allergic (sensitivity) reactions (Zareba et al., 1995). Biofilters have been used for
AN US
centuries to provide clean water for public use (Huisman and Wood, 1974) and
are a viable and cost-effective option for replacement of chemical means of water purification. In addition to the limited crew support, there is a biofilm in the outflow pipe downstream of current treatment and filtration methods that has
Bornemann et al., 2015).
M
persisted after multiple sterilization attempts (Mermel, 2012; Pierson et al., 2012;
ED
2. Biological Filters
PT
Biofilms are surface-associated communities of bacteria and other microorganisms surrounded by an extracellular polymeric matrix (EPS). This EPS
CE
acts as a barrier between the microbes and the environment, protecting them from stressors and allowing sequestration of nutrients (Flemming et al., 2007).
AC
Biological filters (biofilters) containing biofilms have been synthesized using various substrates including sand, soil (Healy et al, 2010), bark, charcoal (Dalameh et al., 2014), and granular activated charcoal (GAC) (Gibert et al., 2013) as the biofilm attachment surface. Biofilters first came into use in 1804,
4
ACCEPTED MANUSCRIPT
when John Gibb of Paisley, Scotland designed a sand filter with the purpose of selling his waste water to the public (Huisman and Wood, 1974). By 1830, the
CR IP T
practice had been adopted by Chelsea Water Company, creating the first historical instance of publically available treated water (Huisman and Wood, 1974). Substrates such as sand in biofilters like Gibb’s function by acting as an
attachment surface for biofilms. In a traditional biofilter, substrate is packed into a
AN US
column and seeded with activated sludge: a community of microbes that are
capable of degrading organic contaminants, including phosphorous-, nitrogen-, and sulfur-containing compounds. In addition to removing organic material, biofilters have also been found to remove over 90% of the initial contaminant
M
bacterial load (Healy et al., 2010).
Each of the various materials that can serve as a substrate for biofilm
ED
growth have benefits and drawbacks for use in spaceflight. Bark and activated
PT
charcoal substrates have been shown to support greater species diversity than sand substrates, leading to removal of more contaminating material. Unfortunately,
CE
bark substrate runs the risk of leeching other organic materials into the water, and granular charcoal could potentially pose a fire risk on ISS. Marble is non-
AC
flammable, biologically inert, and has been shown to be an effective substrate, but sand shares those same qualities and results in more biofilm formation, likely due to the increased surface area (Kadaverugu et al., 2016).
5
ACCEPTED MANUSCRIPT
Sand-based biological filters have been shown to be effective in removing various types of organic material (OM) and in denitrification of wastewater (Vega
CR IP T
et al., 2014), including removal of compounds that tend to be recalcitrant or persistent in water that has been treated by activated sludge (Escola et al., 2015). Biofilms using sand filters are also effective in removing phosphates, sulfates, nitrates, and nitrites, as well as fecal coliforms (Bai et al., 2013; Kahn et al.,
AN US
2015). Alkalinity has also been found to be reduced, which is important in
clearing urine-containing wastewater since the reduction of nitrogen is inhibited under strongly alkaline conditions (Kahn et al., 2015). In addition, as mixed communities, biofilms occupying biofilters are able to be adaptable based on the
M
composition of waste water and can result in a more robust purification of variable types of waste than chemical means of filtration (Bai et al., 2013).
ED
3. Biofilm Growth in Spaceflight Conditions
PT
The most effective way to seed a biofilter is using activated sludge. While certain species have been shown to remove specific contaminants completely
CE
(Zayadan et al., 2014; Alegbeleye et al., 2016; Ruffell et al., 2016; Xiao et al., 2016; Zhao et al., 2016) studies have shown that greater species richness is
AC
correlated with increased removal of contaminant material (Dalameh et al., 2014). Activated sludge is produced in large water treatment facilities, consisting of a vast variety of organisms sourced from the wastewater, and is commonly utilized in municipal water filtration systems. One of the largest difficulties in using a
6
ACCEPTED MANUSCRIPT
biological system as a method of filtration in space is the low gravity environment, termed microgravity. For water filtration in a microgravity
CR IP T
environment, activated sludge can potentially be grown in media representative of the wastewater generated on ISS and serially passaged in modeled microgravity
bioreactors (Schwarz et al., 1992) until the community stabilizes. This will allow
for strains that are stable in microgravitational conditions to dominate the biofilm,
AN US
providing the opportunity for scientists to study and potentially modify those organisms to ensure more complete purification of wastewater. Adapting the biofilm prior to spaceflight will also reduce the likelihood and effect of community changes once microgravity is established.
M
Information on the ability of bacteria to form biofilms under spaceflight conditions is very sparse, though some studies have demonstrated the formation
ED
of biofilms in space (McLean et al., 2001; Rosenzweig et al., 2009; Kim et al.,
PT
2013) and in monocultured species that are capable of growth in microgravity (Rosenzweig et al., 2009; Castro et al., 2011).
CE
4. PVP Coated Silver Nanoparticles as Antibiotics It has long been known that silver has antimicrobial properties (Rogers,
AC
1913). Recently, it has been found that this antibiotic activity is also active in spaceflight conditions (Wong et al., 2010). Polyvinylpyrrolidone (PVP) coated (“capped”) silver nanoparticles (AgNP) also display antibiotic properties (Bryaskova et al., 2011) against a wide range of bacterial species (Bryaskova et
7
ACCEPTED MANUSCRIPT
al., 2011; Bahtia et al., 2016) by rapid release of the colloidal silver at bactericidal concentrations into the environment (Stobie et al., 2008; Bryaskova et al., 2011;
CR IP T
Bhatia et al., 2016). Importantly, release of colloidal silver occurs without releasing the entire delivered volume of AgNP (Dobias and Bernier-Latmani,
2013). In addition to antibacterial activity, PVP coated AgNP has also been found to have antifungal activity (Pereira et al., 2014; Silva et al., 2014). Of particular
AN US
importance, PVP capped AgNPs are capable of passing through biofilters intact, with little adsorption to the biofilm (Li et al., 2013). Unreleased AgNPs are also
able to be recovered from solution by mixing AgNP with magnetic nanoparticles and applying a magnetic field (Mwilu et al., 2014).
M
5. Proposal for Biofilter Design
We propose the design of a biofilter capable of functioning in a
ED
microgravity environment using the above principles. Activated sludge sourced
PT
from a local water treatment plant should be inoculated into a low-shear modeled microgravity (LSMMG) bioreactor to select for organisms capable of growth in
CE
microgravitational conditions. The LSMMG bioreactor is a rotating wall vessel (RWV) that rotates at a set rate to establish solid body rotation of a liquid media,
AC
possible due to the low shear environment in the High Aspect Ratio Vessel (HARV) (Nickerson et al., 2014). Incubation of the activated sludge will allow the community of microorganisms to adjust to the modeled microgravity conditions. Organisms that are incapable of growth in modeled microgravity will
8
ACCEPTED MANUSCRIPT
die off, allowing the organisms capable of growth to flourish. The adapted activated sludge should be used to seed a packed sand column. Additionally, the
CR IP T
sand column would need to be designed with a fine mesh screen on either end of the column to prevent sand from passing out of the column. Wastewater should be passed through the column until the biofilm is established, approximately one month.
AN US
In the assembled biofiltration system, the wastewater, from which large
particulate matter has already been removed, would pass through the intake pipe to the AgNP introduction point, where PVP-coated silver nanoparticles would be added to the wastewater. Immediately after addition of AgNP, the water will flow
M
through the biofilter at an experimentally derived rate that is maintained by pressurizing the water flow. The cleaned water will exit the biofilm, and the
ED
AgNP will release some of the silver, allowing sanitization of the water. Magnetic
PT
nanoparticles will be released into the water, which will sequester the AgNP. A magnet on one side of the outtake pipe will then collect the aggregates of AgNP
CE
and magnetic nanoparticles and direct them to a recycling pipe that will collect the AgNP. The aggregates will flow into a holding container filled with a non-
AC
polar buffer that will allow the separation the AgNP from the magnetic nanoparticles, as well as stabilize the PVP to preserve the AgNP. The magnetic particles will be recycled back into the outtake pipe to collect more AgNP, and the AgNP will be recycled back to the intake pipe to treat more wastewater
9
ACCEPTED MANUSCRIPT
(Figure 2). Released colloidal silver will travel with the treated water to a secondary “recoating” biofilter seeded with bacteria capable of recoating colloidal
CR IP T
silver with PVP, such as Lysinibacillus varians (Bhatia et al., 2016). This biofilter would rotate, applying a centrifugal force to the recoated magnetic particles (Siekmann and Johann, 1976), allowing them to move to the borders of the biofilter where they can be recollected magnetically by residual magnetic
AN US
nanoparticles.
In addition, careful engineering of the orientation of components to switch to filtration based on the gravitational pressure exerted on a planetary surface would result in a filtration system that can be removed from a travel rocket and be
M
implemented in a permanent shelter, particularly useful in future colonization efforts for other planets like Mars. In this case, the system should be designed so
ED
that once it is present on land, in gravity, the pressurizing input can be powered
PT
down, allowing the slow sand filter to work via gravity. This would reduce the energetic input required to produce clean drinking water in newly established
CE
colonies. This would also allow for the size of the crew able to be supported on each colonizing mission to be increased with each rocket that arrives to the
AC
colony. This type of biofilter should reduce operating costs for spaceflight missions by 1) removing the need for membrane-type filters that require frequent changing, 2) eliminating energy-intensive methods of wastewater cleaning, and 3) preventing the requirement for iodine sterilization or other single-use chemical
10
ACCEPTED MANUSCRIPT
methods or treatment. This type of water filter would require less maintenance and fewer changes of replaceable parts, like physical filters, while providing a
CR IP T
safe, purified source of drinking water for both ISS and any future space-flight missions. Acknowledgements
We would like to thank RCJ McLean and the rest of the Slime Gang for their
AN US
support.
Funding: This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.
Author Disclosure Statement: No competing financial interests exist.
M
Figure Legends
Figure 1. Schematic of the PWD on-board the ISS. Overview of the design of
ED
the Russian PWD currently supplying potable water on-board ISS. Courtesy
AC
CE
PT
NASA. (One column)
11
M
AN US
CR IP T
ACCEPTED MANUSCRIPT
ED
Figure 2. Theoretical proposal of new biofilter for spaceflight. Movement of
AC
CE
PT
water through the system is indicated by dashed arrows. (Two column)
12
M
AN US
CR IP T
ACCEPTED MANUSCRIPT
ED
References
PT
Alegbeleye, O. O., Opeolu, B. O., & Jackson, V. (2016). Bioremediation of polycyclic aromatic hydrocarbon (PAH) compounds: (acenaphthene and fluorene) in water using indigenous bacterial species isolated from the Diep and Plankenburg rivers, Western Cape, South Africa. Braz J Microbiol. https://doi.org/10.1016/j.bjm.2016.07.027
CE
Anonymous. (2010). Studying Biofilms on Atlantis Could LEad to Safer, Healthier, Space Travel. Chem Eng Prog, 106(6), 10.
AC
Bai, Y., Liu, R., Liang, J., & Qu, J. (2013). Integrated metagenomic and physiochemical analyses to evaluate the potential role of microbes in the sand filter of a drinking water treatment system. PLoS One, 8(4), e61011. https://doi.org/10.1371/journal.pone.0061011 Bhatia, D., Mittal, A., & Malik, D. K. (2016). Antimicrobial activity of PVP coated silver nanoparticals synthesized by Lysinibacillus varians. 3 Biotech, 6, 196. https://doi.org/10.1007/s13205-016-0514-7
13
ACCEPTED MANUSCRIPT
Bornemann, G., Wasser, K., Tonat, T., Moeller, R., Bohmeier, M., & Hauslage, J. (2015). Natural microbial populations in a water-based biowaste management system for space life support. Life Sci Space Res (Amst), 7, 39– 52. https://doi.org/10.1016/j.lssr.2015.09.002
CR IP T
Boyle, M., Ford, T., Maki, J. S., & Mitchell, R. (1991). Biofilms and the Survival of Opportunistic Pathogens in Recycled Water. Waste Management and Res, 9, 465–470.
AN US
Bryaskova, R., Pencheva, D., Nikolov, S., & Kantardjiev, T. (2011). Synthesis and comparative study on the antimicrobial activity of hybrid materials based on silver nanoparticles (AgNps) stabilized by polyvinylpyrrolidone (PVP). J Chem Biol, 4(4), 185–191. https://doi.org/10.1007/s12154-011-0063-9 Carrasquillo, R. L. (2005). ISS ECLSS Technology Evolution for Exploration. Proceedings of the 43rd American Institute of Aeronautics and Astronautics (AIAA) Aerospaces and Sciences Meeting and Exhibit, AIAA–200–0337.
M
Castro, S. L., Nelman-Gonzalez, M., Nickerson, C. A., & Ott, C. M. (2011). Induction of attachment-independent biofilm formation and repression of Hfq expression by low-fluid-shear culture of Staphylococcus aureus. Appl Environ Microbiol, 77(18), 6368–6378. https://doi.org/10.1128/AEM.0017511
PT
ED
Dalahmeh, S. S., Jonsson, H., Hylander, L. D., Hui, N., Yu, D., & Pell, M. (2014). Dynamics and functions of bacterial communities in bark, charcoal and sand filters treating greywater. Water Res, 54, 21–32. https://doi.org/10.1016/j.watres.2014.01.019
CE
Dobias, J., & Bernier-Latmani, R. (2013). Silver release from silver nanoparticles in natural waters. Environ Sci Technol, 47(9), 4140–4146. https://doi.org/10.1021/es304023p
AC
Escola Casas, M., & Bester, K. (2015). Can those organic micro-pollutants that are recalcitrant in activated sludge treatment be removed from wastewater by biofilm reactors (slow sand filters)? Sci Total Environ, 506-507, 315–322. https://doi.org/10.1016/j.scitotenv.2014.10.113 Flemming, H. C., Neu, T. R., & Wozniak, D. J. (2007). The EPS matrix: the “house of biofilm cells.” J Bacteriol, 189(22), 7945–7947. https://doi.org/10.1128/JB.00858-07
14
ACCEPTED MANUSCRIPT
Gibert, O., Lefevre, B., Fernandez, M., Bernat, X., Paraira, M., Calderer, M., & Martinez-Llado, X. (2013). Characterising biofilm development on granular activated carbon used for drinking water production. Water Res, 47(3), 1101–1110. https://doi.org/10.1016/j.watres.2012.11.026
CR IP T
Hadrup, N., & Lam, H. R. (2014). Oral toxicity of silver ions, silver nanoparticles and colloidal silver--a review. Regul Toxicol Pharmacol, 68(1), 1–7. https://doi.org/10.1016/j.yrtph.2013.11.002
AN US
Healy, M. G., Burke, P., & Rodgers, M. (2010). The use of laboratory sand, soil and crushed-glass filter columns for polishing domestic-strength synthetic wastewater that has undergone secondary treatment. J Environ Sci Health A Tox Hazard Subst Environ Eng, 45(12), 1635–1641. https://doi.org/10.1080/10934529.2010.506130
Huisman, L., & Wood, W. E. (1974). Slow Sand Filtration. (W. H. Organization, Ed.).
M
Hwang, B., Lu, Q., Alves de Toledo, R., & Shim, H. (2016). Enhanced nitrogen removal from sludge reject water by methanol addition using sequencing batch biofilm reactor. Desalination and Water Treatment, 57(19), 8730– 8738. https://doi.org/10.1080/19443994.2015.1022800
ED
Jones, H. W. (2015). Estimating the Life Cycle Cost of Space Systems. 45th International Conference on Environmental Systems, ICES–2015–041.
CE
PT
Kadaverugu, R., Shingare, R. P., Raghunathan, K., Juwarkar, A. A., Thawale, P. R., & Singh, S. K. (2016). The role of sand, marble chips and Typha latifolia in domestic wastewater treatment - a column study on constructed wetlands. Environ Technol, 37(19), 2508–2515. https://doi.org/10.1080/09593330.2016.1153156
AC
Khan, Z. U., Naz, I., Rehman, A., Rafiq, M., Ali, N., & Ahmed, S. (2015). Performance efficiency of an integrated stone media fixed biofilm reactor and sand filter for sewage treatment. Desalination and Water Treatment, 54(10), 2638–2647. https://doi.org/10.1080/19443994.2014.903521 Kim, W., Tengra, F. K., Young, Z., Shong, J., Marchand, N., Chan, H. K., … Collins, C. H. (2013). Spaceflight promotes biofilm formation by Pseudomonas aeruginosa. PLoS One, 8(4), e62437. https://doi.org/10.1371/journal.pone.0062437
15
ACCEPTED MANUSCRIPT
Li, J., Liu, F., Wang, Q., Ge, P., Woo, P. C., Yan, J., … Liu, C. (2014). Genomic and transcriptomic analysis of NDM-1 Klebsiella pneumoniae in spaceflight reveal mechanisms underlying environmental adaptability. Sci Rep, 4, 6216. https://doi.org/10.1038/srep06216
CR IP T
Li, Z., Aly Hassan, A., Sahle-Demessie, E., & Sorial, G. A. (2013). Transport of nanoparticles with dispersant through biofilm coated drinking water sand filters. Water Res, 47(17), 6457–6466. https://doi.org/10.1016/j.watres.2013.08.026
AN US
McLean, R. J. C., Cassanto, J. M., Barnes, M. B., & Koo, J. H. (2001). Bacterial biofilm formation under microgravity conditions. FEMS Microbio Lett, 195, 115–119. Mermel, L. A. (2013). Infection prevention and control during prolonged human space travel. Clin Infect Dis, 56(1), 123–130. https://doi.org/10.1093/cid/cis861
M
Misra, N., Biswal, J., Dhamgaye, V. P., Lodha, G. S., & Sabharwal, S. (2013). A compaterative studt of gamma, electron beam, and synchrotron X-ray irradiation method for synthesis of silver nanoparticles in PVP. Adv Mat Lett, 4(6), 458–463. https://doi.org/10.5185/amlett.2012.ib.114
PT
ED
Mwilu, S. K., Siska, E., Baig, R. B., Varma, R. S., Heithmar, E., & Rogers, K. R. (2014). Separation and measurement of silver nanoparticles and silver ions using magnetic particles. Sci Total Environ, 472, 316–323. https://doi.org/10.1016/j.scitotenv.2013.10.077
CE
Nickerson, C. A., Ott, C. M., Wilson, J. W., Ramamurthy, R., & Pierson, D. L. (2004). Microbial responses to microgravity and other low-shear environments. Microbiol Mol Biol Rev, 68(2), 345–361. https://doi.org/10.1128/MMBR.68.2.345-361.2004
AC
Pereira, L., Dias, N., Carvalho, J., Fernandes, S., Santos, C., & Lima, N. (2014). Synthesis, characterization and antifungal activity of chemically and fungalproduced silver nanoparticles against Trichophyton rubrum. J Appl Microbiol, 117(6), 1601–1613. https://doi.org/10.1111/jam.12652 Pierson, D. L., Botkin, D. J., Bruce, R. J., Castro, V. A., Smith, M. J., Oubre, C. M., & Ott, C. M. (2012). Microbial Monitoring of the International Space Station. In J. Moldenhauer (Ed.), Environmental Monitoring: A
16
ACCEPTED MANUSCRIPT
Comprehensive Handbook (Vol. 6, pp. 1–27). River Grove, IL: DHI Publishing.
CR IP T
Rosenzweig, J. A., Abogunde, O., Thomas, K., Lawal, A., Nguyen, Y. U., Sodipe, A., & Jejelowo, O. (2010). Spaceflight and modeled microgravity effects on microbial growth and virulence. Appl Microbiol Biotechnol, 85(4), 885–891. https://doi.org/10.1007/s00253-009-2237-8
AN US
Ruffell, S. E., Frank, R. A., Woodworth, A. P., Bragg, L. M., Bauer, A. E., Deeth, L. E., … McConkey, B. J. (2016). Assessing the bioremediation potential of algal species indigenous to oil sands process-affected waters on mixtures of oil sands acid extractable organics. Ecotoxicol Environ Saf, 133, 373–380. https://doi.org/10.1016/j.ecoenv.2016.07.034 Schkolnik, G., Schmidt, M., Mazza, M. G., Harnisch, F., & Musat, N. (2015). In Situ Analysis of a Silver Nanoparticle-Precipitating Shewanella Biofilm by Surface Enhanced Confocal Raman Microscopy. PLoS One, 10(12), e0145871. https://doi.org/10.1371/journal.pone.0145871
M
Schwarz, R. P., Goodwin, T. J., & Wolf, D. A. (1992). Cell Culture for ThreeDimensional Modeling in Rotating-Wall Vessels: An Application of Simulated Microgravity. J Tiss Cult Meth, 14, 51–58.
ED
Shaw, L. A., & Barreda, J. L. (2008). International Space Station USOS Potable Water Dispenser Development. SAE Technical Paper, 38th International Conference on Environmental Systems.
CE
PT
Silva, E., Saraiva, S. M., & Miguel, S. P. (2014). PVP-coated silver nanoparticles showing antifungal improved activity against dermatophytes. J Nanopart Res, 16, 2726. https://doi.org/10.1007/s11051-014-2726-2)
AC
Singh, S., Bharti, A., & Meena, V. K. (2015). Green synthesis of multi-shaped silver nanoparticles: optical, morphological and antibacterial properties. J Mater Sci: Mater Electron, 26, 3638–3648. https://doi.org/10.1007/s10854015-2881-y Stobie, N., Duffy, B., McCormack, D. E., Colreavy, J., Hidalgo, M., McHale, P., & Hinder, S. J. (2008). Prevention of Staphylococcus epidermidis biofilm formation using a low-temperature processed silver-doped phenyltriethoxysilane sol-gel coating. Biomaterials, 29(8), 963–969. https://doi.org/10.1016/j.biomaterials.2007.10.057
17
ACCEPTED MANUSCRIPT
Thomas, E. A., Weislogel, M. M., & Klaus, D. M. (2010). Design considerations for sustainable spacecraft water management systems. Adv Space Res, 46, 761–767. https://doi.org/10.1016/j.asr.2010.04.005
CR IP T
Tsukuda, S., Christianson, L., Kolb, A., Saito, K., & Summerfelt, S. (2014). Heterotrophic denitrification of aquaculture effluent using fluidized sand biofilters. Aquacultural Eng, 64, 49–59. https://doi.org/10.1016/j.aquaeng.2014.10.010
Vega, L. M., Alvarez, P. J., & McLean, R. J. (2014). Bacterial signaling ecology and potential applications during aquatic biofilm construction. Microb Ecol, 68(1), 24–34. https://doi.org/10.1007/s00248-013-0321-1
AN US
Wong, W. C., Dudinsky, L. A., Garcia, V. M., Ott, C. M., & Castro, V. A. (2010). Efficacy of various chemical disinfectants on biofilms formed in spacecraft potable water system components. Biofouling, 26(5), 583–586. https://doi.org/10.1080/08927014.2010.495772
M
Xiao, J., Chu, S., Tian, G., Thring, R. W., & Cui, L. (2016). An Eco-tank system containing microbes and different aquatic plant species for the bioremediation of N,N-dimethylformamide polluted river waters. J Hazard Mater, 320, 564–570. https://doi.org/10.1016/j.jhazmat.2016.07.037
ED
Zereba, G., Cernichiari, E., Goldsmith, L. A., & Clarkson, T. W. (1995). Biological Monitoring of Iodine, a Water Disinfectant for Long-term Space Missions. Environ Health Perspectives, 104(11), 1032–1035.
AC
CE
PT
Zhao, Y., Qu, D., Zhou, R., Yang, S., & Ren, H. (2016). Efficacy of forming biofilms by Pseudomonas migulae AN-1 toward in situ bioremediation of aniline-contaminated aquifer by groundwater circulation wells. Environ Sci Pollut Res Int, 23(12), 11568–11573. https://doi.org/10.1007/s11356-0166737-7
18