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对工程化二氧化碳固定大肠杆菌的定量分析揭示了异养二氧化碳固定的巨大潜力。

Quantitative analysis of an engineered CO2-fixing Escherichia coli reveals great potential of heterotrophic CO2 fixation.

作者信息

Gong Fuyu, Liu Guoxia, Zhai Xiaoyun, Zhou Jie, Cai Zhen, Li Yin

机构信息

CAS Key Laboratory of Microbial Physiological and Metabolic Engineering, Institute of Microbiology, Chinese Academy of Sciences, No. 1 West Beichen Road Chaoyang District, Beijing, 100101 China ; University of the Chinese Academy of Sciences, Beijing, China.

CAS Key Laboratory of Microbial Physiological and Metabolic Engineering, Institute of Microbiology, Chinese Academy of Sciences, No. 1 West Beichen Road Chaoyang District, Beijing, 100101 China.

出版信息

Biotechnol Biofuels. 2015 Jun 18;8:86. doi: 10.1186/s13068-015-0268-1. eCollection 2015.

Abstract

BACKGROUND

Production of fuels from the abundant and wasteful CO2 is a promising approach to reduce carbon emission and consumption of fossil fuels. Autotrophic microbes naturally assimilate CO2 using energy from light, hydrogen, and/or sulfur. However, their slow growth rates call for investigation of the possibility of heterotrophic CO2 fixation. Although preliminary research has suggested that CO2 fixation in heterotrophic microbes is feasible after incorporation of a CO2-fixing bypass into the central carbon metabolic pathway, it remains unclear how much and how efficient that CO2 can be fixed by a heterotrophic microbe.

RESULTS

A simple metabolic flux index was developed to indicate the relative strength of the CO2-fixation flux. When two sequential enzymes of the cyanobacterial Calvin cycle were incorporated into an E. coli strain, the flux of the CO2-fixing bypass pathway accounts for 13 % of that of the central carbon metabolic pathway. The value was increased to 17 % when the carbonic anhydrase involved in the cyanobacterial carbon concentrating mechanism was introduced, indicating that low intracellular CO2 concentration is one limiting factor for CO2 fixation in E. coli. The engineered CO2-fixing E. coli with carbonic anhydrase was able to fix CO2 at a rate of 19.6 mg CO2 L(-1) h(-1) or the specific rate of 22.5 mg CO2 g DCW(-1) h(-1). This CO2-fixation rate is comparable with the reported rates of 14 autotrophic cyanobacteria and algae (10.5-147.0 mg CO2 L(-1) h(-1) or the specific rates of 3.5-23.7 mg CO2 g DCW(-1) h(-1)).

CONCLUSIONS

The ability of CO2 fixation was created and improved in E. coli by incorporating partial cyanobacterial Calvin cycle and carbon concentrating mechanism, respectively. Quantitative analysis revealed that the CO2-fixation rate of this strain is comparable with that of the autotrophic cyanobacteria and algae, demonstrating great potential of heterotrophic CO2 fixation.

摘要

背景

利用丰富且被浪费的二氧化碳生产燃料是减少碳排放和化石燃料消耗的一种有前景的方法。自养微生物利用光能、氢能和/或硫能自然同化二氧化碳。然而,它们缓慢的生长速度促使人们研究异养固定二氧化碳的可能性。尽管初步研究表明,将一条二氧化碳固定旁路整合到中心碳代谢途径后,异养微生物固定二氧化碳是可行的,但尚不清楚异养微生物能够固定多少二氧化碳以及固定效率如何。

结果

开发了一个简单的代谢通量指数来指示二氧化碳固定通量的相对强度。当将蓝藻卡尔文循环的两种连续酶整合到大肠杆菌菌株中时,二氧化碳固定旁路途径的通量占中心碳代谢途径通量的13%。当引入参与蓝藻碳浓缩机制的碳酸酐酶时,该值增加到17%,这表明细胞内低二氧化碳浓度是大肠杆菌中二氧化碳固定的一个限制因素。带有碳酸酐酶的工程化二氧化碳固定大肠杆菌能够以19.6 mg CO₂ L⁻¹ h⁻¹的速率或22.5 mg CO₂ g DCW⁻¹ h⁻¹的比速率固定二氧化碳。这个二氧化碳固定速率与报道的14种自养蓝藻和藻类的速率(10.5 - 147.0 mg CO₂ L⁻¹ h⁻¹或3.5 - 23.7 mg CO₂ g DCW⁻¹ h⁻¹的比速率)相当。

结论

通过分别整合部分蓝藻卡尔文循环和碳浓缩机制,在大肠杆菌中创造并提高了二氧化碳固定能力。定量分析表明,该菌株的二氧化碳固定速率与自养蓝藻和藻类的相当,证明了异养固定二氧化碳的巨大潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/56ca/4475311/e3bd8907c2da/13068_2015_268_Fig1_HTML.jpg

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