1.Advances of structure, function, and catalytic mechanism of methyl-coenzyme M reductase.
Zhenli LAI ; Gangfeng HUANG ; Liping BAI
Chinese Journal of Biotechnology 2021;37(12):4147-4157
Methanogens are unique microorganisms for methane production and the main contributor of the biogenic methane in atmosphere. Methyl-coenzyme M reductase (Mcr) catalyzes the last step of methane production in methanogenesis and the first step of methane activation in anaerobic oxidation of methane. The genes encoding this enzyme are highly conserved and are widely used as a marker in the identification and phylogenetic study of archaea. There has been a longstanding interest in its unique cofactor F430 and the underpinning mechanisms of enzymatic cleavage of alkane C-H bond. The recent breakthroughs of high-resolution protein and catalytic-transition-state structures further advanced the structure-function study of Mcr. In particular, the recent discovery of methyl-coenzyme M reductase-like (Mcr-like) enzymes that activates the anaerobic degradation of non-methane alkanes has attracted much interest in the molecular mechanisms of C-H activation without oxygen. This review summarized the advances on function-structure-mechanism study of Mcr/Mcr-like enzymes. Additionally, future directions in anaerobic oxidation of alkanes and greenhouse-gas control using Mcr/Mcr-like enzymes were proposed.
Archaea/metabolism*
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Methane
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Oxidation-Reduction
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Oxidoreductases/metabolism*
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Phylogeny
2.Enhanced heterologous expression of the cytochrome c from uncultured anaerobic methanotrophic archaea.
Lingwei CUI ; Xiaojun FAN ; Yanning ZHENG
Chinese Journal of Biotechnology 2022;38(1):226-237
Cytochrome c is a type of heme proteins that are widely distributed in living organisms. It consists of heme and apocytochrome c, and has potential applications in bioelectronics, biomedicine and pollutant degradation. However, heterologous overexpression of cytochrome c is still challenging. To date, expression of the cytochrome c from uncultured anaerobic methanotrophic archaea has not been reported, and nothing is known about the function of this cytochrome c. A his tagged cytochrome c was successfully expressed in E. coli by introducing a thrombin at the N-terminus of CytC4 and co-expressing CcmABCDEFGH, which is responsible for the maturation of cytochrome c. Shewanella oneidensis, which naturally has enzymes for cytochrome c maturation, was then used as a host to further increase the expression of CytC4. Indeed, a significantly higher expression of CytC4 was achieved in S. oneidensis when compared with in E. coli. The successful heterologous overexpression of CytC4 will facilitate the exploitation of its physiological functions and biotechnological applications.
Anaerobiosis
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Archaea/metabolism*
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Cytochromes c/metabolism*
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Escherichia coli/metabolism*
;
Heme/metabolism*
3.Heat shock proteins of the hyperthermophilic archaea.
Huayou CHEN ; Chunxia ZHANG ; Xiaoke MA ; Yi ZHANG
Chinese Journal of Biotechnology 2008;24(12):2011-2021
As thermostable enzymes and organisms are much more needed, researches on heat shock proteins(HSPs) of hyperthermophilic archaea have drawn more concerns. HSPs from hyperthermophilic archaea are concise only with HSP60, sHSP, prefoldin and AAA+proteins, but without HSP100s, HSP90s, HSP70 (DnaK), HSP40 (DnaJ) and GrpE which are common in mesophilic or thermophilic archaea. Accordingly, studies on the structure, function and operation mechanism of these four groups are much more important and meaningful. This review focuses on the recent progress in the researchs on the structure, function, operation mechanism and cooperation of the HSPs from hyperthermophilic archaea. The problems and obfuscations in these HSPs are analyzed, and farther research direction and key points are put out.
Archaea
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classification
;
metabolism
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Archaeal Proteins
;
metabolism
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Chaperonin 60
;
metabolism
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Heat-Shock Proteins
;
genetics
;
metabolism
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Molecular Chaperones
;
metabolism
4.Expression and characterization of a bifunctional thermal β-glucosidase IuBgl3 from thermophilic archaeon Infirmifilum uzonense.
Xinhan LIU ; Fengfei SHEN ; Pengjun SHI ; Huiqin LIU
Chinese Journal of Biotechnology 2022;38(12):4644-4657
β-glucosidase has important applications in food, medicine, biomass conversion and other fields. Therefore, exploring β-glucosidase with strong stability and excellent properties is a research hotspot. In this study, a GH3 family β-glucosidase gene named Iubgl3 was successfully cloned from Infirmifilum uzonense. Sequence analysis showed that the full length of Iubgl3 was 2 106 bp, encoding 702 amino acids, with a theoretical molecular weight of 77.0 kDa. The gene was cloned and expressed in E. coli and the enzymatic properties of purified IuBgl3 were studied. The results showed that the optimal pH and temperature for pNPG hydrolysis were 5.0 and 85 ℃, respectively. The enzyme has good thermal stability, and more than 85% of enzyme activity can be retained after being treated at 80 ℃ for2 h. This enzyme has good pH stability and more than 85% of its activity can be retained after being treated at pH 4.0-11.0 for 1 h. It was found that the enzyme had high hydrolysis ability to p-nitrophenyl β-d-glucoside (pNPG) and p-nitrophenyl β-d-xylopyranoside (pNPX). When pNPG was used as the substrate, the kinetic parameters Km and Vmax were 0.38 mmol and 248.55 μmol/(mg·min), respectively, and the catalytic efficiency kcat/Km was 6 149.20 s-1mmol-1. Most metal ions had no significant effect on the enzyme activity of IuBgl3. SDS completely inactivated the enzyme, while EDTA increased the enzyme activity by 30%. This study expanded the β-glucosidase gene diversity of the thermophilic archaea GH3 family and obtained a thermostable acid bifunctional enzyme with good industrial application potential.
beta-Glucosidase/chemistry*
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Archaea/metabolism*
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Escherichia coli/metabolism*
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Hydrogen-Ion Concentration
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Temperature
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Glucosides
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Enzyme Stability
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Substrate Specificity
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Kinetics
5.Influence of temperature fluctuation on thermophilic anaerobic digestion of municipal organic solid waste.
Man-chang WU ; Ke-wei SUN ; Yong ZHANG
Journal of Zhejiang University. Science. B 2006;7(3):180-185
A laboratory-scale experiment was carried out to assess the influence of temperature fluctuation on thermophilic anaerobic digestion of municipal organic solid waste (MOSW). Heating failure was simulated by decreasing temperature suddenly from 55 degrees C to 20 degrees C suddenly; 2 h time is needed for temperature decrease and recovery. Under the conditions of 8.0 g/(L.d) and 15 d respectively for MOSW load and retention time, following results were noted: (1) biogas production almost stopped and VFA (volatile fatty acid) accumulated rapidly, accompanied by pH decrease; (2) with low temperature (20 degrees C) duration of 1, 5, 12 and 24 h, it took 3, 11, 56 and 72 h for the thermophilic anaerobic digestion system to reproduce methane after temperature fluctuation; (3) the longer the low temperature interval lasted, the more the methanogenic bacteria would decay; hydrolysis, acidification and methanogenesis were all influenced by temperature fluctuation; (4) the thermophilic microorganisms were highly resilient to temperature fluctuation.
Archaea
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cytology
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physiology
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Bacteria, Anaerobic
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cytology
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physiology
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Biodegradation, Environmental
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Cell Survival
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Cities
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Fatty Acids, Volatile
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metabolism
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Hydrogen-Ion Concentration
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Methane
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metabolism
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Refuse Disposal
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methods
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Sewage
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microbiology
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Temperature