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The microgravity environment of space introduces a major new variable for consideration that will affect the design and operation of bioreactors. Adequate aeration for aerobic bioreactors will be a challenge as will gas/liquid separation, removal of carbon dioxide and other bacterial metabolic waste products, control algorithms, and overall performance assessment. These challenges must be addressed in order to fully assess the efficacy of biological approaches to the recovery of potable water from wastewater in microgravity. The first step in this process is to define the fermentation parameters of the organism or consortia that will be used in these space bioreactors. This study was designed to investigate the ability of bacteria to degrade the space station detergent IGEPON.

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.

Reference cultures of 16 microorganisms obtained from the American Type Culture Collection and four clinical isolates were used in standardized solutions to inoculate 60 cards for each test strain. A set of three ID and three susceptibility cards was processed in the Vitek AutoMicrobic System (AMS) immediately after inoculation. The remaining cards were refrigerated at 4°C, and sets of six cards were removed and processed periodically for up to 17 days. The preinoculated AMS cards were evaluated for microorganism identification, percent probability of correct identification, length of time required for final result, individual substrate reactions, and antibiotic minimal inhibitory concentration (MIC) values. Results indicate that 11 of the 20 microbes tested withstood refrigerated storage up to 17 days without detectable changes in delineating characteristics. MIC results appear variable, but certain antibiotics proved to be more stable than others.

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.

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.

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.

A shower test was conducted recently at NASA-JSC in which waste water was reclaimed and reused. Test subjects showered in a prototype whole body shower following a protocol similar to that anticipated for Space Station. The waste water was purified using reverse osmosis followed by filtration through activated carbon and ion exchange resin beds. The reclaimed waste water was maintained free of microorganisms by using both heat and iodine. This paper discusses the test results, including the limited effectiveness of using iodine as a disinfectant and the evaluation of a Space Station candidate soap for showering. In addition, results are presented on chemical and microbial impurity content of water samples obtained from various locations in the water recovery process.

A microgravity whole body shower (WBS) and a waste water recovery system (WWRS) were used in a closed loop test at the Johnson Space Center. The WWRS process involved chemical pretreatment, phase change distillation and post-treatment. A preprototype Thermoelectric Integrated Hollow Fiber Membrane Evaporation Subsystem (TIMES) was used for distillation after pretreatment and the post-treatment was accomplished with activated carbon, mixed ion exchange resin beds and microbial check valve (MCV) iodine bactericide dispensing units. The purposes of this test were to evaluate a NASA approved Shuttle soap for whole body showering comfort; evaluate the effects of the shower water on the WBS and the TIMES; and evaluate purification qualities of the recovered water in a closed loop operation.