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1.
J Biosci Bioeng ; 137(6): 413-419, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38485553

ABSTRACT

Uracil-thymine dehydrogenase (UTDH), which catalyzes the irreversible oxidation of uracil to barbituric acid in oxidative pyrimidine metabolism, was purified from Rhodococcus erythropolis JCM 3132. The finding of unusual stabilizing conditions (pH 11, in the presence of NADP+ or NADPH) enabled the enzyme purification. The purified enzyme was a heteromer consisting of three different subunits. The enzyme catalyzed oxidation of uracil to barbituric acid with artificial electron acceptors such as methylene blue, phenazine methosulfate, benzoquinone, and α-naphthoquinone; however, NAD+, NADP+, flavin adenine dinucleotide, and flavin mononucleotide did not serve as electron acceptors. The enzyme acted not only on uracil and thymine but also on 5-halogen-substituted uracil and hydroxypyrimidine (pyrimidone), while dihydropyrimidine, which is an intermediate in reductive pyrimidine metabolism, and purine did not serve as substrates. The activity of UTDH was enhanced by cerium ions, and this activation was observed with all combinations of substrates and electron acceptors.


Subject(s)
Oxidation-Reduction , Pyrimidines , Rhodococcus , Uracil , Uracil/metabolism , Uracil/chemistry , Pyrimidines/metabolism , Rhodococcus/enzymology , NADP/metabolism , Methylene Blue/metabolism , Methylene Blue/chemistry , Barbiturates/metabolism , Barbiturates/chemistry , Benzoquinones/metabolism , Benzoquinones/chemistry , Bacterial Proteins/metabolism , Bacterial Proteins/genetics , Bacterial Proteins/chemistry , Hydrogen-Ion Concentration , Thymine/metabolism , Thymine/chemistry , Substrate Specificity , Methylphenazonium Methosulfate/metabolism , Methylphenazonium Methosulfate/chemistry
2.
Elife ; 122023 04 06.
Article in English | MEDLINE | ID: mdl-37022136

ABSTRACT

Life requires ribonucleotide reduction for de novo synthesis of deoxyribonucleotides. As ribonucleotide reduction has on occasion been lost in parasites and endosymbionts, which are instead dependent on their host for deoxyribonucleotide synthesis, it should in principle be possible to knock this process out if growth media are supplemented with deoxyribonucleosides. We report the creation of a strain of Escherichia coli where all three ribonucleotide reductase operons have been deleted following introduction of a broad spectrum deoxyribonucleoside kinase from Mycoplasma mycoides. Our strain shows slowed but substantial growth in the presence of deoxyribonucleosides. Under limiting deoxyribonucleoside levels, we observe a distinctive filamentous cell morphology, where cells grow but do not appear to divide regularly. Finally, we examined whether our lines can adapt to limited supplies of deoxyribonucleosides, as might occur in the switch from de novo synthesis to dependence on host production during the evolution of parasitism or endosymbiosis. Over the course of an evolution experiment, we observe a 25-fold reduction in the minimum concentration of exogenous deoxyribonucleosides necessary for growth. Genome analysis reveals that several replicate lines carry mutations in deoB and cdd. deoB codes for phosphopentomutase, a key part of the deoxyriboaldolase pathway, which has been hypothesised as an alternative to ribonucleotide reduction for deoxyribonucleotide synthesis. Rather than complementing the loss of ribonucleotide reduction, our experiments reveal that mutations appear that reduce or eliminate the capacity for this pathway to catabolise deoxyribonucleotides, thus preventing their loss via central metabolism. Mutational inactivation of both deoB and cdd is also observed in a number of obligate intracellular bacteria that have lost ribonucleotide reduction. We conclude that our experiments recapitulate key evolutionary steps in the adaptation to life without ribonucleotide reduction.


Subject(s)
Ribonucleotide Reductases , Ribonucleotides , Ribonucleotides/metabolism , Escherichia coli/genetics , Escherichia coli/metabolism , Symbiosis , Ribonucleotide Reductases/genetics , Ribonucleotide Reductases/metabolism , Deoxyribonucleotides/metabolism , Deoxyribonucleosides/metabolism
3.
Phys Rev E ; 95(2-1): 021102, 2017 Feb.
Article in English | MEDLINE | ID: mdl-28297999

ABSTRACT

Rayleigh's stability criterion describes the inviscid stability of rotating fluid flows. Despite the limitations of the criterion due to the assumptions used, it has been widely viewed as a general stability barrier in various rapidly rotating flows. However, contrary to previous belief, a linear instability is identified in Rayleigh-stable Taylor-Couette flow. The instability is found in cyclonic rapid rotation regime, for almost the entire range of the radius ratio of the cylinders.

4.
Phys Rev Lett ; 112(18): 184502, 2014 May 09.
Article in English | MEDLINE | ID: mdl-24856700

ABSTRACT

Nonlinear equilibrium states characterized by strongly localized vortex pairs are calculated in the linearly stable parameter region of counterrotating Taylor-Couette flow. These subcritical states are rotating waves whose region of existence is consistent with the critical threshold for relaminarization observed in experiments. For sufficiently rapid outer cylinder rotation the solutions extend beyond the static inner cylinder case to corotation, thus exceeding, for the first time, the boundary defined by the inviscid Rayleigh's stability criterion.

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