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Regulation of Autotrophic and Heterotrophic Metabolism in Pseudomonas oxalaticus OX1:Growth on Mixtures of Acetate and Formate in Continuous Culture

机译:草酸假单胞菌OX1自养和异养代谢的调节:连续培养中乙酸和甲酸盐混合物的生长

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摘要

Growth of Pseudomonas oxalaticus in carbon- and energy-limited continuous cultures with mixtures of acetate and formate resulted in the simultaneous utilization of both substrates at all dilution rates tested. During growth on these mixtures, acetate repressed the synthesis of ribulosebisphosphate carboxylase. The degree of this repression was dependent on the dilution rate and on the ratio of acetate and formate in the medium reservoir. At fixed acetate and formate concentrations in the infiowing medium of 30 and 100 mM, respectively, and dilution rates above 0.10 h-1, the severe repression of autotrophic enzymes resulted in a marked increase in bacterial dry weight compared to the growth yield of the organisms on the two substrates separately. Also, at these dilution rates a significant increase in isocitrate lyase activity was observed in the cells as compared to growth on acetate alone. This indicated that under these conditions more acetate was assimilated and less dissimilated since acetate was partly replaced by formate as the energy source. When formate was added to the reservoir of an acetate-limited culture (SR = 30 mM), derepression of RuBPCase synthesis was observed at formate concentrations of 50 mM and above. Below this concentration formate only served as an energy source for acetate assimilation; when its concentration was increased above 50 mM a progressively increasing contribution of carbon dioxide fixation to the total carbon assimilation was observed as the activity of RuBPCase in the cells increased. It is concluded that in Pseudomonas oxalaticus the synthesis of enzymes involved in autotrophic carbon dioxide fixation via the Calvin cycle is regulated by a repression/derepression mechanism.
机译:草酸假单胞菌在含乙酸和甲酸的混合物的碳和能量有限的连续培养物中的生长导致在所有测试的稀释率下同时利用两种底物。在这些混合物上生长期间,乙酸盐抑制了核糖二磷酸羧化酶的合成。这种抑制的程度取决于稀释率以及培养基储库中乙酸盐和甲酸盐的比率。在流入培养基中乙酸盐和甲酸盐的浓度分别固定为30和100 mM,且稀释速率超过0.10 h-1时,自养酶的严重抑制导致细菌干重与生物体生长量相比显着增加分别放在两个基板上。而且,与仅在乙酸盐上生长相比,在这些稀释率下,在细胞中观察到异柠檬酸裂合酶活性的显着增加。这表明在这些条件下,更多的乙酸被同化,较少的被同化,因为乙酸被一部分甲酸作为能源代替。当将甲酸添加到乙酸盐限制培养物(SR = 30 mM)的储库中时,在50 mM及以上的甲酸浓度下观察到RuBPCase合成的抑制。低于该浓度,甲酸盐仅用作乙酸同化的能量源。当其浓度增加到50 mM以上时,随着细胞中RuBPCase活性的增加,观察到二氧化碳固定对总碳同化作用的贡献逐渐增加。结论是在草假单胞菌中,通过加尔文循环参与参与自养二氧化碳固定的酶的合成受阻抑/抑制机制调节。

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    Dijkhuizen L.; Harder W.;

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  • 年度 1979
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  • 正文语种 eng
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