Soluble extracts of the methanogenic archaeon, Methanosurcina thermophilu TM-l, contained a divalent metal ion-stimulated protein-serine phosphatase activity. This activity was sensitive to micromolar concentrations of okadaic acid, microcystin-LR, or calyculin A, three compounds thought to be highly specific inhibitors of the type 1/2A/2B genetic superfamily of eukaryotic protein-serine/threonine phosphatases. The observation that each of these three chemically unrelated compounds inhibited this archaeal protein phosphatase activity suggests the existence of structural homology, and perhaps even common genetic ancestry, with the type 1/2A/2B superfamily of protein-serine/threonine phosphatases found in eukaryotic organisms.Protein phosphatase; Okadaic acid; Microcystin-LR, Calyculin A, Archaea
A new sequencing method for mixed-model assembly lines is developed and tested. This method, called the Evolutionary Production Sequencer (EPS) is designed to maximize production on an assembly line. The performance of EPS is evaluated using three measures: minimum cycle time necessary to achieve 100% completion without rework, percent of items completed without rework for a given cycle time, and sequence "smoothness." The first two of these measures are based on a simulated production system. Characteristics of the system, such as assembly line station length, assembly time and cycle time, are varied to better gauge the performance of EPS. More fundamental variation is studied by modeling two production systems. In one set of tests, the system consists of an assembly line in isolation (i.e., a single-level system). In another set of tests, the production system consists of the assembly line and the fabrication system supplying components to the line (i.e., a two-level system). Sequence smoothness is measured by the mean absolute deviation (MAD) between actual component usage and the ideal usage at each point in the production sequence.The performance of EPS is compared to those of well-known assembly line sequencing techniques developed by Miltenburg (1 989), Okamura and Yamashina (1979), and Yano and Rachamadugu (1991). EPS performed very well under all test conditions when the criterion of success was either minimum cycle time necessary to achieve 100% production without rework or percent of items completed without rework for a given cycle time. When MAD was the criterion of success, EPS was found inferior to the Miltenburg heuristic but better than the other two production-oriented techniques.
The adenosine analogs neplanocin A and deazaneplanocin A were observed to inhibit the in vivo guanine-7-methylation of mRNA cap structure using a new assay for hypomethylated RNA. Treatment of cultured mammalian cells with these adenosine analogs resulted in the same extent of hypomethylation of cap structure as did ethionine injection in mice. Neplanocin A and its non-metabolizable analog 3deazaneplanocin A show the same maximal level of inhibition of methylation suggesting that these adenosine analogs exert their effects by elevating S-adenosylhomocysteine levels rather than by conversion to other inhibitory compounds.
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