An analysis of vacuum effects in the sterilization of microorganisms
Analysis of vacuum effects in sterilization of microorganisms for planetary quarantine applications
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Analysis of vacuum effects in sterilization of microorganisms for planetary quarantine applications
Microorganism growth supporting or biocidal properties of spacecraft paint coatings
Device, based on gel-impingement technique, collects microorganism specimens from circulating air streams. Device is useful to air pollution studies involving the collection of airborne microbial specimens.
Investigating spacecraft coatings for resistance to growth of microorganisms
Biological effects of thermal environments on dispersal of blue green algae and microorganisms in Iceland and Surtsey
Searching for Precambrian relict microorganism in Iceland
Effect of hard impact and aeolian erosion on release of microorganisms from geological formations
Apollo 11 lunar samples effect on terrestrial microorganisms, noting pigment production effects of Fe leaching from bulk fines and core samples
Simulated Martian environment effects on terrestrial microorganisms survival
Experiments were conducted to determine the effects of microorganisms, substrates, pressures, humidities, and oxygen concentrations upon aluminum corrosion. In addition, the effects of microbes upon coated and treated aluminum were examined and an attempt to correlate aluminum in solution with degradation of the samples was undertaken. The organisms, humidities, oxygen levels, and substrates all played a major role in the corrosion of aluminum. Quantitation of aluminum losses indicated that the total metal losses from inoculated samples were significantly greater than those of the uninoculated samples.
A space molecular sink research facility (Molsink) was used to evaluate the ability of microorganisms to survive the vacuum of outer space. This facility could be programmed to simulate flight spacecraft vacuum environments at pressures in the .1 nanotorr range and thermal gradients (30 to 60 C) closely associated to surface temperatures of inflight spacecraft. Initial populations of Staphylococcus epidermidis and a Micrococcus sp. were reduced approximately 1 log while exposed to -105 and 34 C, and approximately 2 logs while exposed to 59 C for 14 days in the vacuum environment. Spores of Bacillus subtilis var. niger were less affected by the environment. Initial spore populations were reduced 0.2, 0.3, and 0.8 log during the 14-day vacuum exposure at -124, 34, and 59 C, respectively.
Most groups of soil microorganisms died when exposed to prolonged starvation in a carbon-free solution, but the relative abundance of Bacillus and actinomycetes increased with time. Certain nonspore-forming bacteria also persisted. The ability of individual soil isolates to endure starvation in solution was not correlated with their glycogen content or rate of endogenous respiration. However, cells of the resistant populations were rich in poly-beta-hydroxybutyrate, whereas the starvation-susceptible bacteria generally contained little of this substance. Poly-beta-hydroxybutyrate was used rapidly in cells deprived of exogenous sources of carbon.
Microbiological samples were obtained from the crewmembers of the Apollo 13, 14, 15, 16, and 17 spaceflights. These specimens were analyzed for the presence of medically important microorganisms with Staphylococcus aureus, Pseudomonas aeruginosa, Tricophyton mentagrophytes, Tricophyton rubrum, and Candida albicans being discussed in detail. Preflight isolation of crewmembers was found to coincide with a complete absence of inflight disease events and is recommended for future spaceflights. No autoinfection response (microbial shock) occurred after any of the reported spaceflights.
Ammonia production by Klebsiella pneumoniae is not economical with present strains and improving nitrogen fixation to its theoretical limits in this organism is not sufficient to achieve economic viability. Because the value of both the hydrogen produced by this organism and the methane value of the carbon source required greatly exceed the value of the ammonia formed, ammonia (fixed nitrogen) should be considered the by-product. The production of hydrogen by KLEBSIELLA or other anaerobic nitrogen fixers should receive additional study, because the activity of nitrogenase offers a significant improvement in hydrogen production. The production of fixed nitrogen in the form of cell mass by Azotobacter is also uneconomical and the methane value of the carbon substrate exceeds the value of the nitrogen fixed. Parametric studies indicate that as efficiencies approach the theoretical limits the economics may become competitive. The use of nif-derepressed microorganisms, particularly blue-green algae, may have significant potential for in situ fertilization in the environment.
A study was conducted to obtain information concerning the fate of soil microorganisms during the procedures normally used in separating them from the soil in connection with various types of investigations. A silty clay loam (pH 6.0, moisture content 25%, organic content 3.5%) was used in the study. The results of the study indicate that many of the microbial cells naturally residing in soil remain attached to or, for some other reason, are not separated from the soil debris despite the use of various combinations of blending, sonication, and chemical dispersing agents. The method B used by Balkwill et al. (1975) provides a reasonable electron microscopy evaluation of the soil microflora.
An earth-Mars depletion formula proposed by Anders and Owen for volatiles is used to calculate a range of putative Hg levels for Martian volcanic soils based upon analyzed samples from Hawaii. The range is about 50-150 microgram per kg. When applied either in conventional or special media (e.g., basalt powder), these levels of Hg are effective inhibitors of the growth of earth microorganisms. Taken together with other hostile chemical and physical factors, volcanic toxicants would appear to provide a further deterrent to the accidental establishment of terrestrial microbiota on Mars.
Microorganisms were exposed to simulated space environment in order to assess the effect of electrons in the energy range 1 to 5 keV on their colony-forming ability. The test system consisted of an electron gun and power supply, a dosimetry subsystem, and a vacuum subsystem. The system was capable of current densities ranging from 0.1 nA/sq cm to 5 micro A/sq cm on a 25 sq on target and an ultimate vacuum of 0.0006 N/sq m (0.000004 torr). The results of the experimental program show a significant reduction in microbial reproductive integrity.
Microfossils which are preserved as shrivelled kerogenous residues provide little information about cellular organization and almost none about the metabolic properties of the organisms. The distinction between prokaryotic vs eukaryotic, and phototrophic vs chemo- and organotrophic fossil microorganisms rests entirely on morphological comparisons with recent counterparts. The residual nature of the microbial fossil record promotes the conclusion that it must be biased toward (a) most abundant organisms, (b) those most resistant to degradation, and (c) those inhabiting environments with high preservation potential e.g., stromatolites. These criteria support the cyanophyte identity of most Precambrian microbial fossils on the following grounds: (1) as primary producers they dominate prokaryotic communities in modern extreme environments, e.g., intertidal zone; (2) several morphological counterparts of modern cyanophytes and microbial fossils have been established based on structure, cell division patterns and degradation sequences. The impact of anaerobic and oxygenic microbial photosynthesis on the evolution of Precambrian environments is discussed.