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C(1)化合物作为工程恶臭假单胞菌S12的辅助底物。

C(1) compounds as auxiliary substrate for engineered Pseudomonas putida S12.

作者信息

Koopman Frank W, de Winde Johannes H, Ruijssenaars Harald J

机构信息

B-Basic, Delft, The Netherlands.

出版信息

Appl Microbiol Biotechnol. 2009 Jun;83(4):705-13. doi: 10.1007/s00253-009-1922-y. Epub 2009 Mar 12.

Abstract

The solvent-tolerant bacterium Pseudomonas putida S12 was engineered to efficiently utilize the C(1) compounds methanol and formaldehyde as auxiliary substrate. The hps and phi genes of Bacillus brevis, encoding two key steps of the ribulose monophosphate (RuMP) pathway, were introduced to construct a pathway for the metabolism of the toxic methanol oxidation intermediate formaldehyde. This approach resulted in a remarkably increased biomass yield on the primary substrate glucose when cultured in C-limited chemostats fed with a mixture of glucose and formaldehyde. With increasing relative formaldehyde feed concentrations, the biomass yield increased from 35% (C-mol biomass/C-mol glucose) without formaldehyde to 91% at 60% relative formaldehyde concentration. The RuMP-pathway expressing strain was also capable of growing to higher relative formaldehyde concentrations than the control strain. The presence of an endogenous methanol oxidizing enzyme activity in P. putida S12 allowed the replacement of formaldehyde with the less toxic methanol, resulting in an 84% (C-mol/C-mol) biomass yield. Thus, by introducing two enzymes of the RuMP pathway, co-utilization of the cheap and renewable substrate methanol was achieved, making an important contribution to the efficient use of P. putida S12 as a bioconversion platform host.

摘要

对耐溶剂细菌恶臭假单胞菌S12进行工程改造,使其能够高效利用C1化合物甲醇和甲醛作为辅助底物。引入了短短芽孢杆菌的hps和phi基因,它们编码磷酸戊糖(RuMP)途径的两个关键步骤,以构建一条用于代谢有毒甲醇氧化中间体甲醛的途径。当在以葡萄糖和甲醛混合物为食的C限制恒化器中培养时,这种方法导致主要底物葡萄糖的生物量产量显著增加。随着相对甲醛进料浓度的增加,生物量产量从无甲醛时的35%(C-摩尔生物量/C-摩尔葡萄糖)增加到相对甲醛浓度为60%时的91%。表达RuMP途径的菌株也能够在比对照菌株更高的相对甲醛浓度下生长。恶臭假单胞菌S12中存在内源性甲醇氧化酶活性,使得毒性较小的甲醇能够替代甲醛,从而产生84%(C-摩尔/C-摩尔)的生物量产量。因此,通过引入RuMP途径的两种酶,实现了廉价且可再生底物甲醇的共利用,为将恶臭假单胞菌S12高效用作生物转化平台宿主做出了重要贡献。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73c2/2690845/f307dfb800ac/253_2009_1922_Fig1_HTML.jpg

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