Bradyrhizobium japonicum

Agriculture B. japonicum is added to legume seed to improve crop yields, particularly in areas where the bacterium is not native (e.g. Arkansas soils). Often the inoculate is adhered to the seeds prior to planting using a sugar solution. Research A strain of B. japonicum, USDA110, has been in use as a model organism since 1957. It is widely used to study molecular genetics, plant physiology, and plant ecology due to its relatively superior symbiotic nitrogen-fixation activity with soybean (i.e. compared to other rhizobia species). Its entire genome was sequenced in 2002, revealing that the species has a single circular chromosome with 9,105,828 base pairs. ==Metabolism==

B. japonicum is able to degrade catechin with formation of phloroglucinol carboxylic acid, further decarboxylated to phloroglucinol, which is dehydroxylated to resorcinol and hydroxyquinol. B. japonicum possess the nosRZDFYLX gene, which aides in denitrification and has two catalytic subunits - Cu-a and Cu-z (with several histidine residues). It manages an expression cascade that can sense oxygen gradients, termed 'FixJ-FixK2-FixK1.' FixJ positively regulates FixK2, which activates nitrogen respiration genes, as well as FixK1. FixK1 mutants are unable to respire from nitrogen due to a defective catatylic copper subunit (Cu-z) in nosRZDFYLX. ==Genetic transformation==

Natural genetic transformation in bacteria is a sexual process involving transfer of DNA from one cell to another through the intervening medium, and the integration of the donor sequence into the recipient genome by homologous recombination. B. japonicum cells are able to undergo transformation. They become competent for DNA uptake during late log phase. ==References==