Rats were fed diets supplemented with 1% L-methionine with and without 2.5% various amino acids for 7 d to determine what amino acids other than glycine, serine, and cystine can suppress methionine-induced hyperhomocysteinemia. L-Glutamic acid, L-histidine, and L-arginine significantly suppressed methionine-induced enhancement of plasma homocysteine concentrations, but the mechanisms underlying...

We present the proof of the optimality of Threshold Admission and Greedy Scheduling (TAGS) policy under both average and deterministic settings. We first show that EDF-LMO always maintains low cost sources charging plan feasible. Then under the stochastic setting, the admission problem is formulated as a stochastic dynamic programming problem and the optimality of Threshold Admission policy is ...

Salmonella typhimurium possesses a permease specific for L-methionine (K, of 0.1 to 0-2 p ~ ) . Competition studies have shown that the permease has little or no affinity for the other L-amino acids commonly found in proteins. Methionine uptake was competitively inhibited by the growth inhj bitory analogues DLethionine, a-methyl-DL-methionine and DL-methionhe-DL-sulphoximine. Mutants resistant ...

Methionine has been shown to increase plasma cholesterol in animals. In the present study, mechanisms were investigated by which methionine could alter cholesterol metabolism. In the first experiment, forty growing rats were fed four casein-based diets differing in methionine content (2.6, 3.5, 4.5 or 6.0 g/kg) for 14 d. In the second experiment, isolated rat hepatocytes were incubated in media...

The oxidative metabolism of methionine by a transaminative pathway was studied in rat and monkey tissue homogenates. Methionine was shown to undergo transamination followed by subsequent oxidation of its a-keto acid, a-keto-y-methiolbutyrate, to carbon dioxide in rat and monkey liver homogenates. Considerable transamination of methionine was observed in monkey kidney homogenates, but little of ...

Three lines of evidence indicated that methionine sulfoxide is transported by the high-affinity methionine and glutamine transport systems in Salmonella typhimurium. First, methionine-requiring strains (metE) which have mutations affecting both of these transport systems (metP glnP) were unable to use methionine sulfoxide as a source of methionine. These strains could still grow on L-methionine...

A method of 11C-methionine synthesis using ‘bubbling’ method is presented. 11C-methionine was synthesized via 11C methylation from L-cysteine thiolactone (2 mg) in a 300 L solution of 2:1:1 (v/v) 1 M NaOH, ethanol, and water at ambient temperature (85°C, 5 min). The radiochemical purity of radiotracer was higher than 99% and enantiomeric purity (L-11C-methionine) was 91.6 ± 0.4%. The fi nal pr...

The effect on veratryl alcohol production of supplementing cultures of the lignin-degrading fungus Phanerochaete chrysosporium with different methyl-(sup2)H(inf3)-labelled methyl precursors has been investigated. Both chloromethane (CH(inf3)Cl) and l-methionine caused earlier initiation of veratryl alcohol biosynthesis, but S-adenosyl-l-methionine (SAM) retarded the formation of the compound. A...

amounts of methyl incorporation. Other nucleoside triphosphates besides adenosine triphosphate were capable of sup]x>rting the incorjioration of methyl groups from L-methionine into sRNA. The nonspecificity of the nucleoside triphosphate reaction was shown to be due to an adenosine diphosphokinase reaction and not to nucleoside tri phosphate: L-methionine nucleosidyl transferase activity. Mouse...