Evidence for metabolic activity of airborne bacteria

Aerosols of the bacterium Serratia marcescens, and of uniformly labeled C-14 glucose were produced simultaneously and mixed in tubing leading to an aerosol chamber. During a subsequent period of about 5 hrs, carbon dioxide was produced metabolically within the chamber, and labeled material incorporated within the suspended particles first increased then decreased. This constitutes the first direct evidence of microbial metabolism of bacteria suspended in the air

Release of bacterial spores from inner walls of a stainless steel cup subjected to thermal stress

In an earlier report thermal stresses, simulating those expected on a Mars Lander, dislodged approximately 0.01% of an aerosol deposited surface burden, as did a landing shock of 8-10 G deceleration. This work confirms earlier results and demonstrates that release rate is not dependent on surface burden

Possibility of growth of airborne microbes in the Jovian atmosphere

Efforts to show growth activity of anaerobic bacteria in aerosolized particles suspended in anaerobic gas (N2) are described. Evidence of spore generation in nitrogen was obtained. Results are discussed

Studies on propagation of microbes in the airborne state

C-14 metabolic studies on an aerosol mixture of Escherichia coli and a coliphage are indicative of phage production

Possibility of growth of airborne microbes in outer planetary atmospheres

It is shown that airborne bacteria can maintain metabolic functions in a suitable atmosphere. It is theorized that particles in the Jovian atmosphere would have physical half-lives of 10 to 1500 years, depending upon which of two turbulent models is chosen

Studies on possible propagation of microbial contamination in planetary atmospheres

Maintained aerosols were studied to demonstrate the metabolism and propagation of microbes in clouds which could occur in the course of a probe of a planetary atmosphere. Bacteriophage was used as a tool to test whether the mechanisms for DNA production remain intact and functional within the airborne bacterial cell. In one test method, bacteria were mixed with coliphage in an atomizer to allow attachment before aerosolization; in another, two suspensions were atomized saperately into a common air stream prior to aerosolization. Results show that biochemical and physiological mechanisms to allow aerobic microbes to propagate in the airborne state do exist

Evidence for metabolic activity of airborne bacteria

Aerosols of the bacterium Serratia marcescens, and of uniformly labelled C-14 glucose, were created simultaneously and mixed in tubing leading to an aerosol chamber. During a subsequent period of about 5 hrs, C-14O2 was produced unequivocally within the chamber, and insoluble, labelled material within the suspended particles first increased, then decreased

Evidence that bacteria can form new cells in airborne particles.

Serratia marcescens incubated for 8 h at 31 degrees C in a chemically defined medium contained in shake flasks was aerosolized into rotating-drum aerosol chambers at 30 degrees C and saturated humidity. Cells furnished tryptone (Difco) and glycerol just before aerosolization increased (in viable numbers and countable cells) almost twofold within 1 to 2 h after becoming airborne, whereas cells not furnished additional tryptone decreased in viable numbers at a faster rate than the number of particles removed by gravitational settling. Limited tests with a Coulter Counter showed that cell volume changes occurred in growing cells that did not occur in the nongrowing population