首页> 美国卫生研究院文献>Journal of Bacteriology >Biosynthesis of Peptidoglycan in Gaffkya homari: Reactivation of Membranes by Freeze-Thawing in the Presence and Absence of Walls
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Biosynthesis of Peptidoglycan in Gaffkya homari: Reactivation of Membranes by Freeze-Thawing in the Presence and Absence of Walls

机译:Gaffkya homari中肽聚糖的生物合成:在有和没有墙壁的情况下通过冻融来重新活化膜

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摘要

The reactivation of membranes from Gaffkya homari for the synthesis of sodium dodecyl sulfate-insoluble peptidoglycan (SDS-insoluble PG) was achieved by successive cycles of freeze-thawing (− 196 versus 25°C). The presence of G. homari walls during this process affected the synthesis of both SDS-soluble (nascent) and SDS-insoluble PG. At two cycles the synthesis of SDS-soluble PG decreased by 70%, whereas that of SDS-insoluble PG increased sevenfold when compared with membranes reactivated in the absence of walls but assayed in the presence of walls. Moreover, at six cycles the lag time for the synthesis of SDS-insoluble PG decreased from 15 min to 5 to 7 min. Walls from G. homari could not be replaced with walls from Bacillus megaterium or cellulose. In addition to these effects, the presence of walls from G. homari or B. megaterium or of cellulose during the incubation of membranes freeze-thawed in the absence of walls increased twofold the amount of SDS-insoluble PG. Reactivated membranes showed greater sensitivities to penicillin (an inhibitor of dd-carboxypeptidase) and d-methionine (an inhibitor of ld-carboxypeptidase) than did isolated membrane-walls. The percentage of cross-linking of the SDS-insoluble PG synthesized by the reactivated system was 34%, a value similar to that observed for the polymer synthesized by isolated membrane-walls. Freeze-thawing membranes and walls together gave a complex with a density different from that of either membranes or walls. Thus, the assembly system for the synthesis and processing of PG was reconstituted in a complex of membranes and walls prepared from the isolated components. Whether this complex has the exact interrelationship between membrane and wall found in the organism has not been established.
机译:通过连续的冻融循环(-196对25°C)实现了Gaffkya homari膜的活化,以合成十二烷基硫酸钠不溶性肽聚糖(SDS不溶性PG)。此过程中霍马弧菌壁的存在影响了SDS可溶(新生)和SDS不溶PG的合成。与没有壁但在有壁的情况下重新活化的膜相比,在两个循环中,SDS可溶性PG的合成减少了70%,而SDS不溶性PG的合成增加了七倍。此外,在六个循环中,合成不溶于SDS的PG的延迟时间从15分钟减少到5至7分钟。 G. homari的墙壁无法用巨大芽孢杆菌或纤维素的墙壁代替。除了这些作用外,在没有壁的情况下冻融的膜温育过程中,霍马链霉菌或巨大芽孢杆菌壁或纤维素壁的存在使不溶于SDS的PG的量增加了两倍。与分离的膜壁相比,重新活化的膜对青霉素(dd-羧肽酶的抑制剂)和d-蛋氨酸(ld-羧肽酶的抑制剂)的敏感性更高。通过重新活化的系统合成的SDS不溶性PG的交联百分比为34%,该值类似于通过隔离的膜壁合成的聚合物所观察到的值。冻融的膜和壁在一起形成的复合物的密度不同于膜或壁的密度。因此,用于PG的合成和加工的组装系统被重构为由分离的组分制备的膜和壁的复合物。这种复合物是否在生物体中发现的膜与壁之间具有确切的相互关系尚未确定。

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