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Space flight and related factors such as stress appear to have an adverse effect on astronauts' immune systems. The presence of potentially pathogenic microbes including several genera of fungi reported from spacecraft environment may be a cause of concern in such situations. In order to study the role of such organisms in causing opportunistic or allergic diseases in crewmembers, we have tried to develop an animal model. BALB/c mice were suspended upside down for varying periods of time to induce stress, and their lymphocyte functions were evaluated. These studies indicate that the stress resulted in lowered mitogen induced lymphocyte stimulation as represented by 3H-thymidine uptake. We have also studied the ability of these animals to respond to Aspergillus fumigatus spores. The results of the study clearly demonstrate a definite down-regulation in T-cell proliferation and a higher incidence of infection with A. fumigatus.

Small, highly polar organics such as urea, alcohols, acetone, and glycols are not easily removed by the International Space Station's Water Recovery System. The current design utilizes the Volatile Removal Assembly (VRA) which operates at 125°C to catalytically oxidize these contaminants. Since decomposition of these organics under milder conditions would be beneficial, several ambient temperature biocatalytic and catalytic processes were evaluated in our laboratory. Enzymatic oxidation and ambient temperature heterogeneous catalytic oxidation of these contaminants were explored. Oxidation of alcohols proceeded rapidly using alcohol oxidase; however, effective enzymes to degrade other contaminants except urea were not found. Importantly, both alcohols and glycols were efficiently oxidized at ambient temperature using a highly active, bimetallic noble metal catalyst.

Biofilms form rapidly on surfaces in contact with the water reclamation systems proposed for long-term space travel. These microbial populations pose a potentially serious hazard to the astronauts, the engineering systems and to the function of plant growth chambers. Human pathogens present in grey water survive for long periods on surfaces, protected against disinfection by the presence of a biofilm matrix. In addition, some of the materials being proposed for use in water reclamation systems for the orbiting space station are highly susceptible to microbial degradation. Both blockage and corrosion can occur as a result of the interactions between the microorganisms and the materials. Chemicals produced by microbial processes during growth on surfaces include both metals and organic toxins. These by-products of metabolic activity are potential hazards to astronaut health and growth of plants being considered as part of the life support system.

Two simulated spacecraft water systems are being used to evaluate the effectiveness of iodine for controlling microbial contamination within such systems. An iodine concentration of about 2.0 mg/L is maintained in one system by passing ultrapure water through an iodinated ion exchange resin. Stainless steel coupons with electropolished and mechanically-polished sides are being used to monitor biofilm formation. Results after three years of operation show a single episode of significant bacterial growth in the iodinated system when the iodine level dropped to 1.9 mg/L. This growth was apparently controlled by replacing the iodinated ion exchange resin, thereby increasing the iodine level. The second batch of resin has remained effective in controlling microbial growth down to an iodine level of 1.0 mg/L. Scanning electron microscopy indicates that the iodine has impeded but may have not completely eliminated the formation of biofilm.

The ability of iodine to maintain microbial water quality in a simulated spacecraft water system is being studied. An iodine level of about 2.0 mg/L is maintained by passing ultrapure influent water through an iodinated ion exchange resin. Six liters are withdrawn daily and the chemical and microbial quality of the water is monitored regularly. Stainless steel coupons used to monitor biofilm formation are being analyzed by culture methods, epifluorescence microscopy, and scanning electron microscopy. Results from the first two years of operation show a single episode of high bacterial colony counts in the iodinated system. This growth was apparently controlled by replacing the iodinated ion exchange resin. Scanning electron microscopy indicates that the iodine has limited but not completely eliminated the formation of biofilm during the first two years of operation.

Several solid waste management (SWM) systems currently under development for spacecraft deployment result in the production of a variety of toxic gaseous contaminants. Examples include the Plastic Melt Waste Compactor (PMWC) at NASA - Ames Research Center1, the Oxidation/Pyrolysis system at Advanced Fuel Research2, and the Microwave Powered Solid Waste Stabilization and Water Recovery (MWSWS&WR) System at UMPQUA Research Company (URC). The current International Space Station (ISS) airborne contaminant removal system, the Trace Contaminant Control Subassembly (TCCS), is designed to efficiently process nominal airborne contaminants in spacecraft cabin air. However, the TCCS has no capability to periodically process the highly concentrated toxic vapors of variable composition, which are generated during solid waste processing, without significant modifications.

The investigation and development of a chemiluminescence based ethanol detection concept into a biosensor system is described. The biosensor uses alcohol oxidase to catalyze the reaction of short chain primary alcohols with elemental oxygen to produce hydrogen peroxide and the corresponding aldehyde. The reaction of hydrogen peroxide with an organic luminophore in the presence of a sufficient electric field results in emission of blue light with peak intensity at 425nm. The chemiluminescent light intensity is directly proportional to the alcohol concentration of the sample. The aqueous phase chemistry required for sensor operation is implemented using solid phase modules which adjust the pH of the influent stream, catalyze the oxidation of alcohol, provide the controlled addition of the luminophore to the flowing aqueous stream, and minimize the requirement for expendables. Precise control of the pH has proven essential for the long-term sustained release of the luminophore.

Microbial film formation throughout the water reclamation systems proposed for use in the NASA Space Station Freedom poses serious corrosion risks. Choice of materials for construction of these systems must include evaluation of the potential for microbially influenced corrosion. The development of an active and therefore potentially corrosive microbial biofilm on metal surfaces is influenced by the nature of the metal substratum. This has been shown by scanning electron microscopy, isolation and identification of attached bacteria and measurements of biomass and activity. However, these techniques do not allow direct ‘ real-time’ measurement of biofilm formation and subsequent materials degradation. This is necessary to assess the efficacy of biocides and alternative remedial measures. This paper presents potential fouling and corrosion problems associated with water reclamation system design for the NASA orbiting space station.

In 1985, the Man-Systems Division at the Johnson Space Center initiated a program for the development of a whole body shower suitable for operation in a microgravity environment. Supporting this development effort has been a systematic research program focused on four critical aspects of the design (i.e., human factors engineering, biomedical, mechanical, and electrical) and on the interfaces between the whole body shower system and the other systems to be aboard the Space Station (e.g., the water reclamation and air revitalization systems). A series of tests has been conducted to help define the design requirements for the whole body shower. Crew interface research has identified major design parameters related to enclosure configurations, consumable quantities, operation timelines, displays and controls, and shower and cleanup protocols.

Magnetically Assisted Gasification (MAG) is a relatively new concept for the destruction of solid wastes aboard spacecraft, lunar and planetary habitations. Three sequential steps are used to convert the organic constituents of waste materials into useful gases: filtration, gasification, and ash removal. In the filtration step, an aqueous suspension of comminuted waste is separated and concentrated using a magnetically consolidated depth filter composed of granular ferromagnetic media. Once the filter is fully loaded, the entrapped solids are thermochemically gasified via a variety of mechanisms including pyrolysis, isomerization, and oxidation reactions. Finally, the inorganic ash residue is removed from the magnetic media by fluidization and trapped downstream by filtration. Importantly, for each of these steps, the degree of consolidation or fluidization of the granular ferromagnetic media is controlled using magnetic forces.

In-flight contamination control has been an important concern of NASA since the first manned missions. Previous experience has shown that uncontrolled growth of bacteria and fungi can have a detrimental effect on both the health of the crew and the proper operation of flight hardware. It is therefore imperative to develop a safe, effective method of microbial control. Spacecraft application dictates a more stringent set of requirements for biocide selection than is usually necessary for terrestrial situations. Toxicity of the biocide is the driving factor for disinfectant choice in spacecraft. This concern greatly reduces the number and types of chemical agents that can be used as disinfectants. Currently, four biocide candidates (hydrogen peroxide, quaternary ammonium compounds, iodine, glutaraldehyde) are being evaluated as potential surface disinfectants for Space Station Freedom.

We evaluated the ability of a 3% (8800 μM) solution of hydrogen peroxide to kill 12 strains of bacteria and 12 strains of fungi. A 1:4 dilution of 3% H2O2, equivalent to 1100 μM, was lethal to all the tested strains. If the situation calls for a nonaggressive disinfectant without residue or toxic aftereffects, 3% H2O2 seems an ideal choice.

Controlling microbial growth and biofilm formation in spacecraft water-distribution systems is necessary to protect the health of the crew. Methods to decontaminate the water system in flight may be needed to support long-term missions. We evaluated the ability of iodine and ozone to kill attached bacteria and remove biofilms formed on stainless steel coupons. The biofilms were developed by placing the coupons in a manifold attached to the effluent line of a simulated spacecraft water-distribution system. After biofilms were established, the coupons were removed and placed in a treatment manifold in a separate water treatment system where they were exposed to the chemical treatments for various periods. Disinfection efficiency over time was measured by counting the bacteria that could be recovered from the coupons using a sonication and plate count technique. Scanning electron microscopy was also used to determine whether the treatments actually removed the biofilm.

The active control of problematic microbial populations aboard spacecraft, and within future lunar and planetary habitats is a fundamental Advanced Life Support (ALS) requirement to ensure the long-term protection of crewmembers from infectious disease, and to shield materials and equipment from biofouling and biodegradation. The development of effective antimicrobial coatings and materials is an important first step towards achieving this goal and was the focus of our research. A variety of materials were coated with antibacterial and antifungal agents using covalent linkages. Substrates included both granular media and materials of construction. Granular media may be employed to reduce the number of viable microorganisms within flowing aqueous streams, to inhibit the colonization and formation of biofilms within piping, tubing and instrumentation, and to amplify the biocidal activity of low aqueous iodine concentrations.

This paper provides an assessment of functional characteristics needed in the microbial water analysis system being developed for Space Station. Available technology is reviewed with respect to performing microbial monitoring, isolation, or identification functions. An integrated system composed of three different technologies is presented.

Novel mesoporous bimetallic oxidation catalysts are described, which are currently under development for the deep oxidation (mineralization) of aqueous organic contaminants in wastewater produced on-board manned spacecraft, and lunar and planetary habitats. The goal of the ongoing development program is to produce catalysts capable of organic contaminant mineralization near ambient temperature. Such a development will significantly reduce Equivalent System Mass (ESM) for the ISS Water Processor Assembly (WPA), which must operate at 135°C to convert organic carbon to CO2 and carboxylic acids. Improvements in catalyst performance were achieved due to the unique structural characteristics of mesoporous materials, which include a three-dimensional network of partially ordered interconnected mesopores (5-25 nm).

Weightlessness, cosmic radiation and other space flight related conditions may adversely impact the physiology and immune status of the crew. Since microorganisms will surely be present in space habitats, the effects of space on microbial metabolic and physiologic functions will depend upon environmental conditions, types of organisms, and the duration of the flight. Because humans will conduct long-duration space missions, space microbiology must address the effect of alterations in microbial function during space flight. Even innocuous microorganisms and endogenous flora may become etiologic agents for disease during long missions. The microbial population in the closed environments of spacecraft may also become a source of toxic metabolites or the biodegradation of materials. This paper reviews studies concerning microbial behavior in closed environments, simulated microgravity, and actual space flight.

To mitigate risk to crew health, the microbial surveillance of the quality of potable water sources of the International Space Station (ISS) has been ongoing since before the arrival of the first permanent crew. These water sources have included stored ground-supplied water, water produced by the Shuttle fuel cells during flight, and ISS humidity condensate that is reclaimed and processed. In-flight monitoring was accomplished using a self-contained filtering system designed to allow bacterial growth and enumeration during flight. Upon return to Earth, microbial isolates were identified using 16S ribosomal gene sequencing. While the predominant isolates were common Gram negative bacteria including Ralstonia eutropha, Methylobacterium fujisawaense, and Sphingomonas paucimobilis, opportunistic pathogens such as Stenotrophomonas maltophilia and Pseudomonas aeruginosa were also isolated.

One of the proposed methods for monitoring the microbial quality of the water supply aboard the International Space Station is membrane filtration. We adapted this method for space flight by using an off-the-shelf filter unit developed by Millipore. This sealed unit allows liquid to be filtered through a 0.45 μm cellulose acetate filter that sits atop an absorbent pad to which growth medium is added. We combined a tetrazolium dye with R2A medium to allow microbial colonies to be seen easily, and modified the medium to remain stable over 70 weeks at 25°C. This hardware was assembled and tested in the laboratory and during parabolic flight; a modified version was then flown on STS-66. After the STS-66 mission, a back-up plastic syringe and an all-metal syringe pump were added to the kit, and the hardware was used successfully to evaluate water quality aboard the Russian Mir space station.

With the restructure and funding changes for Space Station Freedom, the Environmental Health System (EHS)/Microbiology Subsystem revised its scheduling and operational requirements for component hardware. The function of the Microbiology Subsystem is to monitor the environmental quality of air, water, and internal surfaces and, in part, crew health on board Space Station. Its critical role shall be the identification of microbial contaminants in the environment that may cause system degradation, produce unsanitary or pathogenic conditions, or reduce crew and mission effectiveness. EHS/Microbiology operations and equipment shall be introduced in concert with a phased assembly sequence, from Man Tended Capability (MTC) through Permanently Manned Capability (PMC). Effective Microbiology operations and subsystem components will assure a safe, habitable, and useful spacecraft environment for life sciences research and long-term manned exploration.