The Exometabolome of Clostridium Thermocellum Reveals Overflow Metabolism at High Cellulose Loading

BackgroundClostridium thermocellum is a model thermophilic organism for the production of biofuels from lignocellulosic substrates. The majority of publications studying the physiology of this organism use substrate concentrations of ≤10 g/L. However, industrially relevant concentrations of substrate start at 100 g/L carbohydrate, which corresponds to approximately 150 g/L solids. To gain insight into the physiology of fermentation of high substrate concentrations, we studied the growth on, and utilization of high concentrations of crystalline cellulose varying from 50 to 100 g/L by C. thermocellum.

The Exometabolome of Clostridium Thermocellum Reveals Overflow Metabolism at High Cellulose Loading

BackgroundClostridium thermocellum is a model thermophilic organism for the production of biofuels from lignocellulosic substrates. The majority of publications studying the physiology of this organism use substrate concentrations of ≤10 g/L. However, industrially relevant concentrations of substrate start at 100 g/L carbohydrate, which corresponds to approximately 150 g/L solids. To gain insight into the physiology of fermentation of high substrate concentrations, we studied the growth on, and utilization of high concentrations of crystalline cellulose varying from 50 to 100 g/L by C. thermocellum.

Finishing the euchromatic sequence of the human genome

The sequence of the human genome encodes the genetic instructions for human physiology, as well as rich information about human evolution. In 2001, the International Human Genome Sequencing Consortium reported a draft sequence of the euchromatic portion of the human genome. Since then, the international collaboration has worked to convert this draft into a genome sequence with high accuracy and nearly complete coverage. Here, we report the result of this finishing process. The current genome sequence (Build 35) contains 2.85 billion nucleotides interrupted by only 341 gaps. It covers ∼99% of the euchromatic genome and is accurate to an error rate of ∼1 event per 100,000 bases. Many of the remaining euchromatic gaps are associated with segmental duplications and will require focused work with new methods. The near-complete sequence, the first for a vertebrate, greatly improves the precision of biological analyses of the human genome including studies of gene number, birth and death. Notably, the human enome seems to encode only 20,000-25,000 protein-coding genes. The genome sequence reported here should serve as a firm foundation for biomedical research in the decades ahead

Altered Herbivore Distribution Associated With Focal Disturbance

Natural disturbances historically created structurally diverse patterns across the landscape, and large herbivores concentrated herbivory in areas where disturbance decreased standing senesced biomass that acted as a grazing deterrent through decreased palatability and overall forage quality. However, following European settlement, many natural large-scale disturbance regimes that influence vegetation and herbivore grazing selection were altered or removed and replaced with fine-scale anthropogenic disturbances. It is unclear how fine-scale focal disturbance and alteration of vegetation structure influences livestock distribution and grazing. Therefore we used a tracked vehicle as a disturbance agent in a mesic mixed-grass prairie to assess the influence of focal anthropogenic disturbance on livestock distribution and grazing. Track vehicle disturbance decreased the height of vegetation (P0.05). Cattle fecal pat density was greater (P 0.05) between tracked and nontracked locations following the second growing season. Therefore, we concluded that fine-scale focal anthropogenic disturbance alters herbivore distribution and defoliation and can maintain structural heterogeneity, but the effect is ephemeral and does not create long-lasting grazing lawns. The Rangeland Ecology & Management archives are made available by the Society for Range Management and the University of Arizona Libraries. Contact [email protected] for further information.Migrated from OJS platform August 202