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环磷酸腺苷和挥发性物质在毛霉状网柄菌大囊形成菌株发育中的可能作用:(环磷酸腺苷/酸碱度/大囊/分化/毛霉状网柄菌)

The Possible Involvement of Cyclic AMP and Volatile Substance (s) in the Development of a Macrocyst-Forming Strain of Dictyostelium mucoroides: (cyclic AMP/pH/macrocyst/differentiation/Dictyostelium mucoroides).

作者信息

Amagai Aiko, Filosa Michael F

机构信息

Department of Zoology, Scarborough College, University of Toronto West Hill, Ontario, Canada.

出版信息

Dev Growth Differ. 1984;26(6):583-589. doi: 10.1111/j.1440-169X.1984.00583.x.

Abstract

A mutant MF1 previously isolated from Dictyostelium mucoroides-7 (Dm7) formed macrocysts with or without light when plated on agar at high cell dinsities. At lower cell densities, however, the MF1 cells formed only fruiting bodies. This failure to form macrocysts was shown to be due to the subthreshfold concentration of a volatile substance(s) required for macrocyst formation. Although ammonia is a volatile substance produced by both the Dm7 and MF1 cells, no evidence of its involvement in macrocyst formation was obtained. Mixing the Dm7 and MF1 in a one-to-one ratio resulted only in fruiting body formation suggesting that the Dm7 cells produced a factor which allowed MF1 cells to form fruiting bodies. This factor may be cyclic AMP (cAMP) since addition of cAMP to the medium directed development of MF1 cells to fruiting body formation. The effect of cAMP was exhibited most conspicuously when MF1 cells were exposed at the aggregation stage. Based on these results it is suggested that developmental pathway of the D. mucoroides macrocystforming strain Dm7 and its mutant MF1 may be determined by the relative concentrations of the volatile, macrocyst-inducing substance(s) and cAMP at the aggregation stage.

摘要

一种先前从黏液网柄菌-7(Dm7)中分离出的突变型MF1,当以高细胞密度接种在琼脂上时,无论有无光照都会形成大囊泡。然而,在较低细胞密度下,MF1细胞仅形成子实体。这种无法形成大囊泡的情况被证明是由于大囊泡形成所需的挥发性物质浓度低于阈值。尽管氨是Dm7和MF1细胞都会产生的挥发性物质,但没有证据表明其参与大囊泡的形成。将Dm7和MF1以1:1的比例混合只会导致子实体形成,这表明Dm7细胞产生了一种因子,使MF1细胞能够形成子实体。这种因子可能是环磷酸腺苷(cAMP),因为向培养基中添加cAMP会引导MF1细胞发育形成子实体。当MF1细胞在聚集阶段暴露时,cAMP的作用最为明显。基于这些结果,有人提出黏液网柄菌大囊泡形成菌株Dm7及其突变体MF1的发育途径可能由聚集阶段挥发性的、诱导大囊泡形成的物质和cAMP的相对浓度决定。

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