Words similar to mycobacterium
Example sentences for: mycobacterium
How can you use “mycobacterium” in a sentence? Here are some example sentences to help you improve your vocabulary:
Deinococcus-Synechocystis-Mycobacterium
Mfas: Macaca fascicularis , Mjan: Methanococcus jannaschii , Mka: Methanopyrus kandleri , Mlo: Mesorhizobium loti , Mma: Methanosarcina mazei , Mta: Methanothermobacter thermautotrophicus , Mtu: Mycobacterium tuberculosis , Nm: Neisseria meningitidis , Oih: Oceanobacillus iheyensis , Osa: Oryza sativa , Pa: Pyrococcus abyssi , Pae: Pseudomonas aeruginosa , Pfu: Pyrococcus furiosus , Ph: Pyrococcus horikoshii , Pmar: Prochlorococcus marinus , Pmu: Pasteurella multocida , Pyae: Pyrobaculum aerophilum , Rsol: Ralstonia solanacearum , Sa: Staphylococcus aureus , Scoe: Streptomyces coelicolor , Sen: Salmonella enterica , Sme: Sinorhizobium meliloti , Spn: Streptococcus pneumoniae , Spy: Streptococcus pyogenes , Sso: Sulfolobus solfataricus , Ssp: Synechocystis sp.
The relaxation and decatenation activities of T. maritima topoisomerase I appear to be significantly more efficient than those of the E. coli topoisomerase I [ 33 ] . Based on their primary sequences, a number of bacterial topoisomerase I enzymes do not appear to coordinate any Zn(II) with tetracysteines motifs while other type IA topoisomerase has up to 4 tetracysteine motifs [ 7 ] . The topoisomerase I from Mycobacterium smegmatis has been demonstrated biochemically not to bind Zn(II) [ 34 ] . In contrast, mutation disrupting the fourth Zn(II) motif of Helicobacter pylori topoisomerase I abolished enzyme function in vivo [ 35 ] . Therefore there may be significant differences in the mechanisms of type IA topoisomerases from different organisms with respect to requirement of Zn(II) binding for relaxation activity.
The sequences of the proteins encoded in complete genomes were extracted from the Genome division of the Entrez retrieval system [ 34 ] . The analyzed genomes included those of 30 bacteria: Aquifex aeolicus (Aquae), Bacillus halodurans (Bacha), Bacillus subtilis (Bacsu), Borrelia burgdorferi (Borbu), Buchnera sp. (Bucsp), Campylobacter jejunii (Camje), Caulobacter crescentus (Caucr), Chlamydia trachomatis (Chltr), Chlamydophila pneumoniae (Chlpn), Deinococcus radiodurans (Deira), Escherichia coli (Escco), Haemophilus influenzae (Haein), Helicobacter pylori (Helpy), Lactococcus lactis (Lacla), Mesorhizobium loti (Meslo), Mycoplasma genitalium (Mycge), Mycoplasma pneumoniae (Mycpn), Mycobacterium tuberculosis (Myctu),
However, only one rRNA operon is present in each subspecies and this is also true for the fast growers Mycobacterium abscessus and Mycobacterium chelonae [ 32 ] . These fast growing mycobacteria have multiple promoters that increase the transcriptional rate of the rRNA operon to overcome gene dosage limitations [ 32 ] . The rRNA operon promoter structures have not been mapped by primer extension for either M. paratuberculosis or M. avium , but if M. avium had multiple functional rRNA operon promoters, that may account for the growth rate differences.
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