scholarly journals Adaptation of anammox bacteria to low temperature via gradual acclimation and cold shocks: distinctions in protein expression, membrane composition and activities

2021 ◽  
pp. 117822
Author(s):  
Kouba V ◽  
Vejmelkova D ◽  
Zwolsman E ◽  
Hurkova K ◽  
Navratilova K ◽  
...  
2021 ◽  
Author(s):  
V. Kouba ◽  
D. Vejmelkova ◽  
E. Zwolsman ◽  
K. Hurkova ◽  
K. Navratilova ◽  
...  

AbstractAnammox bacteria enable an efficient removal of nitrogen from sewage in processes involving partial nitritation and anammox (PN/A) or nitrification, partial denitrification, and anammox (N-PdN/A). In mild climates, anammox bacteria must be adapted to ≤15 °C, typically by gradual temperature decrease; however, this takes months or years. To reduce the time necessary for the adaptation, an unconventional method of ‘cold shocks’ is promising, involving hours-long exposure of anammox biomass to extremely low temperatures. We compared the efficacies of gradual temperature decrease and cold shocks to increase the metabolic activity of anammox (fed batch reactor, planktonic “Ca. Kuenenia”). We assessed the cold shock mechanism on the level of protein expression (quantitative shot-gun proteomics, LC-HRMS/MS) and structure of membrane lipids (UPLC-HRMS/MS). The shocked culture was more active (0.66±0.06 vs 0.48±0.06 kg-N/kg-VSS/d) and maintained the relative content of N-respiration proteins at levels consistent levels with the initial state, whereas the content of these proteins decreased in gradually acclimated culture. Cold shocks also induced a more efficient up-regulation of cold shock proteins (e.g. CspB, TypA, ppiD). Ladderane lipids characteristic for anammox evolved to a similar end-point in both cultures which confirms their role in anammox bacteria adaptation to cold and indicates a three-pronged adaptation mechanism involving ladderane lipids (ladderane alkyl length, introduction of shorter non-ladderane alkyls, polar headgroup). Overall, we show the outstanding potential of cold shocks for low-temperature adaptation of anammox bacteria and provide yet unreported detailed mechanisms of anammox adaptation to low temperatures.HighlightsAnammox bacteria were adapted to low T by gradual acclimation and cold shocksThe shocked culture was more active (0.66±0.06 vs 0.48±0.06 kg-N/kg-VSS/d)N-respiration proteins content decreased in gradually acclimated bacteriaSeveral cold shock proteins were upregulated more efficiently by cold shocksAt ↓T, anammox adjusted ladderane membrane lipid composition in three aspectsGraphical abstract


Crop Science ◽  
2013 ◽  
Vol 53 (4) ◽  
pp. 1571-1580 ◽  
Author(s):  
Xiujuan Lei ◽  
Yingping Wang ◽  
Changyu Li ◽  
Chengguo Zhang ◽  
Juan Song ◽  
...  

2007 ◽  
Vol 73 (15) ◽  
pp. 4849-4856 ◽  
Author(s):  
Ryoma Miyake ◽  
Jun Kawamoto ◽  
Yun-Lin Wei ◽  
Masanari Kitagawa ◽  
Ikunoshin Kato ◽  
...  

ABSTRACT A recombinant protein expression system working at low temperatures is expected to be useful for the production of thermolabile proteins. We constructed a low-temperature expression system using an Antarctic cold-adapted bacterium, Shewanella sp. strain Ac10, as the host. We evaluated the promoters for proteins abundantly produced at 4°C in this bacterium to express foreign proteins. We used 27 promoters and a broad-host-range vector, pJRD215, to produce β-lactamase in Shewanella sp. strain Ac10. The maximum yield was obtained when the promoter for putative alkyl hydroperoxide reductase (AhpC) was used and the recombinant cells were grown to late stationary phase. The yield was 91 mg/liter of culture at 4°C and 139 mg/liter of culture at 18°C. We used this system to produce putative peptidases, PepF, LAP, and PepQ, and a putative glucosidase, BglA, from a psychrophilic bacterium, Desulfotalea psychrophila DSM12343. We obtained 48, 7.1, 28, and 5.4 mg/liter of culture of these proteins, respectively, in a soluble fraction. The amounts of PepF and PepQ produced by this system were greater than those produced by the Escherichia coli T7 promoter system.


2015 ◽  
Vol 81 (16) ◽  
pp. 5519-5526 ◽  
Author(s):  
Xin-Wei Yang ◽  
Hua-Hua Jian ◽  
Feng-Ping Wang

ABSTRACTA low-temperature-inducible protein expression vector (pSW2) based on a filamentous phage (SW1) of the deep-sea bacteriumShewanella piezotoleransWP3 was constructed. This vector replicated stably inEscherichia coliandShewanellaspecies, and its copy number increased at low temperatures. The pSW2 vector can be utilized as a complementation plasmid in WP3, and it can also be used for the production of complex cytochromes with multiple heme groups, which has the potential for application for metal ion recovery or bioremediation. Promoters of low-temperature-inducible genes in WP3 were fused into the vector to construct a series of vectors for enhancing protein expression at low temperature. The maximum green fluorescent protein intensity was obtained when the promoter for thehfqgene was used. The WP3/pSW2 system can efficiently produce a patatin-like protein (PLP) from a metagenomic library that tends to form inclusion bodies inE. coli. The yields of PLP in the soluble fraction were 8.3 mg/liter and 4.7 mg/liter of culture at 4°C and 20°C, respectively. Moreover, the pSW2 vector can be broadly utilized in otherShewanellaspecies, such asS. oneidensisandS. psychrophila.


2015 ◽  
Vol 362 (10) ◽  
Author(s):  
Eoin Gunnigle ◽  
Alma Siggins ◽  
Catherine H. Botting ◽  
Matthew Fuszard ◽  
Vincent O'Flaherty ◽  
...  

2014 ◽  
Vol 175 (2) ◽  
pp. 909-924 ◽  
Author(s):  
Xiu-Yun Yuan ◽  
Fang Liang ◽  
Su-Hua Jiang ◽  
Mo-Fei Wan ◽  
Jie Ma ◽  
...  

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