Budd K, Sussman A S, Eilers F I
J Bacteriol. 1966 Feb;91(2):551-61. doi: 10.1128/jb.91.2.551-561.1966.
Budd, Kenneth (The University of Michigan, Ann Arbor), Alfred S. Sussman, and Frederick I. Eilers. Glucose-C(14) metabolism of dormant and activated ascospores of Neurospora. J. Bacteriol. 91:551-561. 1966.-Dormant and activated ascospores of Neurospora tetrasperma, incubated in C(14)-labeled glucose, absorb and metabolize this sugar. At the same time, up to 55% of the CO(2) production from endogenous substrates is quenched, whereas total CO(2) production is unchanged. Glucose-carbon appears in CO(2), lipids, and ethyl alcohol-soluble and -insoluble material in both dormant and activated ascospores, although the proportions entering these fractions differ in the two groups of spores. With few exceptions, the identifiable intermediates of glucose metabolism are the same in dormant and activated ascospores, indicating that the principal pathways may be identical. During glucose metabolism, dormant ascospores accumulate a nondialyzable, ethyl alcohol-soluble polymer, or polymers, which is either absent from activated spores or present in much smaller amounts. This material contains glucose, ribose, and at least nine amino acids, and may represent precursors of more complex cell material which accumulate because of an enzymatic deficiency in the dormant spore. Radioactivity is incorporated into all fractions of the dormant spores and into CO(2) without a noticeable lag, indicating that most, if not all, of the enzymes for glucose utilization are present. A lag in incorporation is observed in the activated spores, which most probably is due to rapid endogenous production of glucose from trehalose, resulting in dilution of lable. After absorption of labeled glucose, two pools of trehalose are found in dormant spores, one of which is extractable without breaking the spores, and the other, only after the spores are disintegrated. The widely differing specific radioactivity of the two pools indicates that these are separated in the intact spore.
巴德,肯尼斯(密歇根大学,安阿伯分校)、阿尔弗雷德·S·苏斯曼和弗雷德里克·I·艾勒斯。粗糙脉孢菌休眠和活化子囊孢子的葡萄糖 - C(14) 代谢。《细菌学杂志》91:551 - 561。1966年。——将粗糙脉孢菌的休眠和活化子囊孢子在C(14) 标记的葡萄糖中培养,它们会吸收并代谢这种糖。与此同时,内源性底物产生的二氧化碳中高达55% 被抑制,而总二氧化碳产量不变。葡萄糖碳出现在休眠和活化子囊孢子的二氧化碳、脂质以及乙醇可溶和不可溶物质中,尽管进入这些组分的比例在两组孢子中有所不同。除了少数例外,休眠和活化子囊孢子中可识别的葡萄糖代谢中间产物是相同的,这表明主要途径可能是一样的。在葡萄糖代谢过程中,休眠子囊孢子积累一种不可透析的、乙醇可溶的聚合物,或多种聚合物,活化孢子中要么不存在这种物质,要么含量少得多。这种物质含有葡萄糖、核糖和至少九种氨基酸,可能代表更复杂细胞物质的前体,由于休眠孢子中的酶缺陷而积累。放射性物质在没有明显延迟的情况下被整合到休眠孢子的所有组分和二氧化碳中,这表明用于葡萄糖利用的大多数(如果不是全部)酶都存在。在活化孢子中观察到放射性物质整合有延迟,这很可能是由于海藻糖快速内源性产生葡萄糖,导致标记物稀释。吸收标记葡萄糖后,在休眠孢子中发现了两个海藻糖池,其中一个在不破坏孢子的情况下即可提取,另一个只有在孢子解体后才能提取。两个池的比放射性差异很大,表明它们在完整孢子中是分开的。