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Control of the Life Cycle of Methanosarcina mazei S-6 by Manipulation of Growth Conditions

机译:通过操纵生长条件来控制甲蛋白酶毛明丸的生命周期

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The morphology of Methanosarcina mazei was controlled by magnesium, calcium, and substrate concentrations and by inoculum size; these factors allowed manipulation of the morphology and interconversions between pseudosarcinal aggregates and individual, coccoid cells. M. mazei grew as aggregates in medium with a low concentration of catabolic substrate (either 50 mM acetate, 50 mM methanol, or 10 mM trimethylamine) unless Ca2+ and Mg2+ concentrations were high. Growth in medium high in Ca2+, Mg2+, and substrate (i.e., 150 mM acetate, 150 mM methanol, or 40 mM trimethylamine) converted pseudosarcinal aggregates to individual cocci. In such media, aggregates separated into individual cells which continued to grow exclusively as single cells during subsequent transfers. Conversion of single cells back to aggregates was complicated, because conditions which supported the aggregated morphology (e.g., low calcium or magnesium concentration) caused lysis of coccoid inocula. We recovered aggregates from coccoid cells by inoculating serial dilutions into medium high in calcium and magnesium. Cells from very dilute inocula grew into aggregates which disaggregated on continued incubation. However, timely transfer of the aggregates to medium low in calcium, magnesium, and catabolic substrates allowed continued growth as aggregates. We demonstrated the activity of the enzyme (disaggregatase) which caused the dispersion of aggregates into individual cells; disaggregatase was produced not only during disaggregation but also in growing cultures of single cells. Uronic acids, the monomeric constituents of the Methanosarcina matrix, were also produced during disaggregation and during growth as coccoids.
机译:Methanosarcina mazei的形态由镁,钙和底物浓度和接种物尺寸控制;这些因素允许操纵假序列聚集体和个体,手式手球菌之间的形态和互联。除非Ca2 +和Mg2 +浓度高,米Mazei含有低浓度的分解代谢基质(50mM乙酸酯,50mM甲醇或10mM三甲胺)的聚集体。 Ca2 +,Mg2 +和底物中培养基(即150mM乙酸盐,150mM甲醇或40mM三甲胺)转化为单个COCC1的培养基中的生长转化为单个COCC1。在这种介质中,分离成单个细胞的聚集体继续在后续转移期间仅作为单细胞的单独生长。将单细胞转化回聚集体是复杂的,因为支持聚集形态(例如,低钙或低钙或镁浓度)的条件使得晕辣皮接种裂解。我们通过将连续稀释液接种到钙和镁中的中等高中,从Coccoid细胞中回收聚集体。来自非常稀疏的接种物的细胞增入聚集体,其在继续孵育时分解。然而,及时将聚集体转移到钙,镁和分解代谢底物中的中低低位允许持续生长为聚集体。我们证明了酶(脱粒酶)的活性,其使聚集体分散成单个细胞;不仅在分解过程中不仅在分解过程中制备了脱粒酶,而且在单细胞的生长培养物中产生。在分解期间也产生弥合溶剂酸,甲蛋白酶基质的单体成分,并在生长期间作为手球糖。

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