首页> 美国卫生研究院文献>Journal of Bacteriology >Regulation of phosphoglycerate phosphomutase in developing forespores and dormant and germinated spores of Bacillus megaterium by the level of free manganous ions.
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Regulation of phosphoglycerate phosphomutase in developing forespores and dormant and germinated spores of Bacillus megaterium by the level of free manganous ions.

机译:游离芽孢杆菌中游离锰离子水平对巨大芽孢杆菌发育中的孢子休眠芽和萌发芽孢中磷酸甘油酸磷酸酯酶的调节。

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摘要

The large depot of phosphoglyceric acid (PGA) which is accumulated within spores of Bacillus megaterium is greater than 99% 3-phosphoglyceric acid (3-PGA). The 3-PGA depot is stable in forespores and dormant spores, but is utilized rapidly during spore germination. When spores were germinated in KBr plus NaF, the PGA depot was not utilized, but 13% of the 3-PGA was converted to 2-PGA. These data suggest phosphoglycerate phosphomutase as the enzyme which is regulated to allow 3-PGA accumulation during sporulation. Young isolated forespores, in which 3-PGA was normally stable, utilized their 3-PGA rapidly when incubated with Mn2+ plus the divalent cation ionophore X-537A; Mn2+ or ionophore alone or Mg2+ or Ca2+ plus ionophore was without effect. Young forespores contained significant amounts of Mn2+. However, forespore Mn2+ exchanged slowly with exogenous Mn2+ and was removed poorly by toluene treatment. This suggests that much of the forespore Mn2+ is tightly bound to some forespore component. Since phosphoglycerate phosphomutase from B. megaterium has an absolute and specific requirement for Mn2+, these data suggest that the activity of this enzyme in vivo may be regulated to a large degree by the level of free Mn2+. Indeed, the activity of this enzyme in forespore or dormant spore extracts was stimulated greater than 25-fold by Mn2+, whereas comparable extracts from cells or germinated spores were stimulated only two- to fourfold.
机译:巨大芽孢杆菌的孢子中积累的磷酸甘油酸(PGA)的较大储库大于99%的3-磷酸甘油酸(3-PGA)。 3-PGA库在前孢子和休眠孢子中稳定,但在孢子萌发过程中被快速利用。当孢子在KBr加NaF中发芽时,没有使用PGA库,但是13%的3-PGA转化为2-PGA。这些数据表明磷酸甘油酸磷酸变位酶是被调节以允许在孢子形成过程中3-PGA积累的酶。分离出的幼小前孢子通常与3-PGA保持稳定,当与Mn2 +加二价阳离子离子载体X-537A一起孵育时,它们迅速利用了3-PGA。 Mn2 +或离子载体或Mg2 +或Ca2 +离子载体均无效。年轻的前孢子含有大量的Mn2 +。然而,前孢子Mn2 +与外源性Mn2 +交换缓慢,并通过甲苯处理很难去除。这表明大部分前孢子Mn2 +与某些前孢子组分紧密结合。由于来自巨大芽孢杆菌的磷酸甘油酸磷酸变位酶对Mn2 +具有绝对和特定的要求,因此这些数据表明该酶的体内活性可能在很大程度上受游离Mn2 +的水平调节。实际上,Mn2 +刺激该酶在前孢子或休眠孢子提取物中的活性大于25倍,而来自细胞或发芽孢子的类似提取物仅被刺激了2到4倍。

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