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通过低效调节的碳流对解纤维梭菌的生长抑制

Growth inhibition of Clostridium cellulolyticum by an inefficiently regulated carbon flow.

作者信息

Guedon E, Desvaux M, Payot S, Petitdemange H

出版信息

Microbiology (Reading). 1999 Aug;145 ( Pt 8):1831-1838. doi: 10.1099/13500872-145-8-1831.

Abstract

Carbon flow in Clostridium cellulolyticum was investigated either in batch or continuous culture using a synthetic medium with cellobiose as the sole source of carbon and energy. Previous experiments carried out using a complex growth medium led to the conclusion that the carbon flow was stopped by intracellular NADH. In this study, results showed that cells cultured in a synthetic medium were better able to control electron flow since the NADH/NAD+ ratios were in the range 0.3-0.7, whereas a ratio as high as 57 was previously found in cells cultured on a complex medium. Furthermore, a specific rate of cellobiose consumption of 2.13 mmol (g cells)-1 h-1 was observed on synthetic medium whereas the highest value obtained on complex medium was 0.68 mmol (g cells)-1 h-1. When C. cellulolyticum was grown in continuous culture and cellobiose in the feed medium was increased from 5.84 to 17.57 mM in stepwise fashion, there was an increase in cellobiose utilization without growth inhibition. In contrast, when the reactor was fed directly with 14.62 mM cellobiose, residual cellobiose was observed (4.24 mM) and growth was limited. These data indicate that C. cellulolyticum is not able to optimize its growth and carbon flow in response to a sudden increase in the concentration of growth substrate cellobiose. This interpretation was confirmed (i) by the study of cellobiose batch fermentation where it was demonstrated that growth inhibition was not due to nutritional limitation or inhibition by fermentation products but was associated with carbon excess and (ii) by the growth of C. cellulolyticum in dialysis culture where no growth inhibition was observed due to the limitation of carbon flow by the low rate of cellobiose diffusion through the dialysis tubing.

摘要

利用以纤维二糖作为唯一碳源和能源的合成培养基,在分批培养或连续培养条件下研究了纤维分解梭菌中的碳流。先前使用复杂生长培养基进行的实验得出结论,碳流被细胞内的NADH阻断。在本研究中,结果表明,在合成培养基中培养的细胞能够更好地控制电子流,因为NADH/NAD⁺比率在0.3 - 0.7范围内,而先前在复杂培养基上培养的细胞中发现该比率高达57。此外,在合成培养基上观察到纤维二糖的比消耗速率为2.13 mmol(g细胞)⁻¹ h⁻¹,而在复杂培养基上获得的最高值为0.68 mmol(g细胞)⁻¹ h⁻¹。当纤维分解梭菌在连续培养中生长,且进料培养基中的纤维二糖以逐步方式从5.84 mM增加到17.57 mM时,纤维二糖利用率增加且无生长抑制。相反,当直接向反应器中加入14.62 mM纤维二糖时,观察到有残留纤维二糖(4.24 mM)且生长受限。这些数据表明,纤维分解梭菌无法响应生长底物纤维二糖浓度的突然增加而优化其生长和碳流。这一解释通过以下两点得到证实:(i)纤维二糖分批发酵研究表明,生长抑制不是由于营养限制或发酵产物抑制,而是与碳过量有关;(ii)纤维分解梭菌在透析培养中的生长情况表明,由于纤维二糖通过透析管的扩散速率低导致碳流受限,未观察到生长抑制。

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