N-carbamoyl-beta-D(+)-glucopyranosylamine metabolism by rumen microbes.

Degradation of N-carbamoyl-beta-D(+)-glucopyranosylamine (NCG) by rumen microorganisms in vitro required a viable population as it did not occur if the microbial preparation had been sterilized. Production of CO2 from glucose, or the glucose portion of NCG, was not affected by acetohydroxamic acid (AHA), but urea hydrolysis was inhibited by 79%. With N-[14C]carbamoyl-beta-D(+)-glucopyranosylamine, production of 14CO2 decreased and [14C]urea accumulated when AHA was included in the medium. Cell-free rumen fluid did not degrade NCG. These observations support the hypothesis that the first nitrogenous component formed from the degradation of NCG is urea.

Evaluation of test media for routine monitoring of Escherichia coli in nonpotable waters.

Six test media, m-TEC, m-TEC with 4-methylumbelliferyl-beta-D-glucuronide (MUG), lauryl tryptose agar (LTA) with MUG, LTA with 5-bromo-4-chloro-3-indolyl-beta-D-glucuronide (X-Glue), EC medium with MUG, and lauryl tryptose broth with MUG, were evaluated for their usefulness in enumerating Escherichia coli in nonpotable waters on a routine basis. The media were chosen for their case of interpretation of target colonies, ability to allow enumeration at low and high concentrations, and ability to inhibit nontarget microorganisms. The recoveries on the test media were compared with those on three reference media, R2A, m-FC, and m-Endo, by analysis of spiked samples of filter-sterilized waters. The test media were then further tested for their ability to differentiate nontarget but closely related microorganisms. Statistical analysis indicated that the best recoveries were obtained with lauryl tryptose agar with added MUG and X-Gluc. The media were then tested with surface waters that could be expected to have high levels of total and fecal coliforms along with Escherichia coli.

Urbanization and the microbial content of the north Saskatchewan River.

The effect of urbanization on the microbial content of the North Saskatchewan River was determined by following the changes in the numbers of total bacteria, total eosin methylene blue (EMB) plate count, and Escherichia coli as the river flowed from its glacial source, through parklands, and out into the prairies. Changes in physical parameters such as pH, temperature, salt concentration, and the amount and nature of the suspended material were also determined to evaluate their on the microbial parameters being measured. The level of all three microbial parameters studied slowly increased as the river flowed from its glacial source out into the prairies. The major effect of small hamlets, with or without sewage treatment facilities, appears to be to supply nutrients which supports the growth of the indigenous river flora but not E. coli. In contrast, the effect of a large urban center, with a population of approximately 500,000, which utilizes primary and secondary sewage processes in disposing of sewage, is to provide the nutrients and an inoculum of E. coli which results in a marked increase in the numbers of all three microbial groups studied. The effect of this urban center was still discernible 300 miles downstream. The river was also monitored for the presence of Salmonella sp. Only one positive isolation was achieved during this study, and this isolate was characterized as being Salmonella alachua.

Formation of bacterial microcolonies on feed particles in the rumen.

Examination of particulate feed that had been digested in vivo in the rumen, and of the leaves of specific legumes that had been digested in vitro by a mixed population of rumen bacteria, showed that very extensive glycocalyx-enclosed bacterial microcolonies developed on many of the available surfaces. Some of these adherent bacteria colonized a surface almost exclusively and attracted another specific type of bacteria as the second members of a distinct morphological consortium. The true extent of the exopolysaccharide glycocalyces of these adherent rumen bacteria was seen in cases where the fibers were attached at multiple points, and their role in microcolony formation and adhesion could be unequivocally ascribed.

A study of predominant aerobic microflora of black bears (Ursus americanus) and grizzly bears (Ursus arctos) in northwestern Alberta.

Swab specimens were obtained from nasal, rectal, and preputial or vaginal areas of 37 grizzly and 17 black bears, captured during May to June of 1981 to 1983, to determine the types and frequency of predominant aerobic microflora. Bacterial genera most frequently isolated from bears were Escherichia, Citrobacter, Hafnia, Proteus, Staphylococcus, and Streptococcus species, comprising about 65% of the isolates. Erwinia, Xanthomonas, Agrobacterium, Rhizobium, and Gluconobacter/Acetobacter were also isolated but at lower frequencies (less than 5%). Comparison of bacterial generic composition using similarity quotient values showed no appreciable differences between grizzly and black bear flora. Also, no outstanding differences in bacterial generic composition were observed among grizzly bear samples; however, differences were noted among black bear samples. Fungal genera most commonly encountered included Cryptococcus, Rhodotorula, Cladosporium, Penicillium, Sporobolomyces, and Candida. In general, the microflora of both bear types were marked by generic diversity and random distribution. The majority of microorganisms isolated from the plant samples in the study area were also found in bear samples. This observation and the presence of certain water and soil bacteria in samples from bears suggest that the predominant microflora of both grizzly and black bears were transient and probably influenced by their foraging habits and surrounding environments.