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1.
Microbiologyopen ; 9(7): e1047, 2020 07.
Article in English | MEDLINE | ID: mdl-32352651

ABSTRACT

Halophilic archaea from the genus Halorubrum possess two extraordinarily diverged archaellin genes, flaB1 and flaB2. To clarify roles for each archaellin, we compared two natural Halorubrum lacusprofundi strains: One of them contains both archaellin genes, and the other has the flaB2 gene only. Both strains synthesize functional archaella; however, the strain, where both archaellins are present, is more motile. In addition, we expressed these archaellins in a Haloferax volcanii strain from which the endogenous archaellin genes were deleted. Three Hfx. volcanii strains expressing Hrr. lacusprofundi archaellins produced functional filaments consisting of only one (FlaB1 or FlaB2) or both (FlaB1/FlaB2) archaellins. All three strains were motile, although there were profound differences in the efficiency of motility. Both native and recombinant FlaB1/FlaB2 filaments have greater thermal stability and resistance to low salinity stress than single-component filaments. Functional supercoiled Hrr. lacusprofundi archaella can be composed of either single archaellin: FlaB2 or FlaB1; however, the two divergent archaellin subunits provide additional stabilization to the archaellum structure and thus adaptation to a wider range of external conditions. Comparative genomic analysis suggests that the described combination of divergent archaellins is not restricted to Hrr. lacusprofundi, but is occurring also in organisms from other haloarchaeal genera.


Subject(s)
Archaeal Proteins/genetics , Flagellin/genetics , Halorubrum/genetics , Halorubrum/metabolism , Locomotion/genetics , Base Sequence , DNA, Archaeal/genetics , Halorubrum/classification , Polymerase Chain Reaction
2.
J Org Chem ; 84(17): 11068-11079, 2019 Sep 06.
Article in English | MEDLINE | ID: mdl-31409063

ABSTRACT

The atom transfer radical addition reaction catalyzed by triphenylphosphine and copper(I) halide is described. The reaction proceeds under irradiation with 365 nm light using a light-emitting diode and was performed in regular glassware. The proposed mechanism involves the formation of quaternary phosphonium salt, which undergoes single electron reduction by copper(I) salt via photo-induced electron transfer. The method works well for terminal alkenes and activated organic halides such as esters of bromo- and iodoacetic acid and bromoacetonitrile. gem-Difluorinated styrenes, for which atom transfer reactions are rare, also proved to be good substrates for this phosphine-/copper-catalyzed protocol.

3.
Microbiologyopen ; 8(5): e00718, 2019 05.
Article in English | MEDLINE | ID: mdl-30270530

ABSTRACT

Microorganisms require a motility structure to move towards optimal growth conditions. The motility structure from archaea, the archaellum, is fundamentally different from its bacterial counterpart, the flagellum, and is assembled in a similar fashion as type IV pili. The archaellum filament consists of thousands of copies of N-terminally processed archaellin proteins. Several archaea, such as the euryarchaeon Haloarcula marismortui, encode multiple archaellins. Two archaellins of H. marismortui display differential stability under various ionic strengths. This suggests that these proteins behave as ecoparalogs and perform the same function under different environmental conditions. Here, we explored this intriguing system to study the differential regulation of these ecoparalogous archaellins by monitoring their transcription, translation, and assembly into filaments. The salt concentration of the growth medium induced differential expression of the two archaellins. In addition, this analysis indicated that archaellation in H. marismortui is majorly regulated on the level of secretion, by a still unknown mechanism. These findings indicate that in archaea, multiple encoded archaellins are not completely redundant, but in fact can display subtle functional differences, which enable cells to cope with varying environmental conditions.


Subject(s)
Archaeal Proteins/metabolism , Cell Surface Extensions/metabolism , Gene Expression Regulation, Archaeal/drug effects , Haloarcula marismortui/metabolism , Macromolecular Substances/metabolism , Protein Multimerization , Salts/metabolism , Culture Media/chemistry , Haloarcula marismortui/drug effects , Haloarcula marismortui/growth & development , Protein Biosynthesis , Protein Transport , Transcription, Genetic
4.
J Org Chem ; 82(24): 12967-12974, 2017 12 15.
Article in English | MEDLINE | ID: mdl-29172505

ABSTRACT

A method for the synthesis of diversely substituted 3-fluoropyridines from two ketone components is described. The reaction involves photoredox coupling of α,α-difluoro-ß-iodoketones with silyl enol ethers catalyzed by fac-Ir(ppy)3 under blue LED irradiation with subsequent one-pot condensation with ammonium acetate. Based on cyclic voltammetry studies, it was determined that α,α-difluoro-ß-iodoketones are reduced notably easier compared to 2,2,2-trifluoro-1-iodoethane, which may be ascribed to the influence of the carbonyl group.

5.
J Org Chem ; 82(6): 3270-3275, 2017 03 17.
Article in English | MEDLINE | ID: mdl-28218543

ABSTRACT

A method for the synthesis of 3-hydroxy-4,4-difluoropyrrolidines from α,α-difluoro-ß-bromoketones is described. The reaction involves methylenation of the carbonyl group with tetrahydrothiophenium ylide followed by coupling with primary amines.

6.
J Org Chem ; 81(19): 9455-9460, 2016 10 07.
Article in English | MEDLINE | ID: mdl-27627651

ABSTRACT

A new fluorinated silicon reagent bearing a functionalized tetrafluoroethylene fragment was prepared from two CF2 building blocks: ethyl bromodifluoroacetate and (bromodifluoromethyl)trimethylsilane. The key C-C bond-forming step involves a difluorocarbene addition/cyclopropane rearrangement sequence. The silicon reagent was coupled with aldehydes and reactive azomethines in the presence of potassium fluoride.

7.
J Org Chem ; 80(11): 5870-6, 2015 Jun 05.
Article in English | MEDLINE | ID: mdl-25965426

ABSTRACT

A method for the difluorohomologation of ketones accompanied by halogenation of a C-H bond is described. The reaction involves silylation, difluorocarbene addition using Me3SiCF2Br activated by a bromide ion, and halogenation of intermediate cyclopropanes with N-bromo- or N-iodosuccinimide. The whole process is performed without isolation of intermediates. The resulting α,α-difluoro-ß-halo-substituted ketones can be readily converted into fluorine containing pyrazole derivatives and oxetanes.


Subject(s)
Ethers, Cyclic/chemical synthesis , Hydrocarbons, Fluorinated/chemistry , Ketones/chemistry , Pyrazoles/chemical synthesis , Bromosuccinimide/chemistry , Catalysis , Ethers, Cyclic/chemistry , Halogenation , Hydrogen Bonding , Molecular Structure , Pyrazoles/chemistry , Succinimides/chemistry
8.
Sci Rep ; 5: 7736, 2015 Jan 13.
Article in English | MEDLINE | ID: mdl-25583370

ABSTRACT

Designing a new generation of energy-intensive and sustainable electrode materials for batteries to power a variety of applications is an imperative task. The use of biomaterials as a nanosized structural template for these materials has the potential to produce hitherto unachievable structures. In this report, we have used genetically modified flagellar filaments of the extremely halophilic archaea species Halobacterium salinarum to synthesize nanostructured iron oxide composites for use as a lithium-ion battery anode. The electrode demonstrated a superior electrochemical performance compared to existing literature results, with good capacity retention of 1032 mAh g(-1) after 50 cycles and with high rate capability, delivering 770 mAh g(-1) at 5 A g(-1) (~5 C) discharge rate. This unique flagellar filament based template has the potential to provide access to other highly structured advanced energy materials in the future.


Subject(s)
Electric Power Supplies , Flagella/physiology , Lithium/chemistry , Oxides/chemistry , Computer Simulation , Electrochemical Techniques , Electrodes , Genes, Archaeal , Halobacterium/genetics , Minerals , Monte Carlo Method
9.
Extremophiles ; 18(2): 341-9, 2014 Mar.
Article in English | MEDLINE | ID: mdl-24368632

ABSTRACT

The genome of haloarchaeon Haloarcula marismortui contains two archaellin genes-flaA2 and flaB. Earlier we isolated and characterized two H. marismortui strains in that archaella consisting of FlaA2 archaellin (with a minor FlaB fraction) or of FlaB only. Both the FlaA2 and FlaB strains were motile and produced functional helical archaella. Thus, it may seem that the FlaA2 archaellin is redundant. In this study we investigated the biological roles of archaellin redundancy and demonstrated that FlaA2 archaellin is better adapted to more severe conditions of high temperature/low salinity, while FlaB has an advantage with increasing salinity. We used the thermodynamic data and bioinformatics sequence analysis to demonstrate that archaella formed by FlaA2 are more stable than those formed by FlaB. Our combined data indicate that the monomer FlaA2 archaellin is more flexible and leads to more compact and stable formation of filamentous structures. The difference in response to environmental stress indicates that FlaA2 and FlaB replace each other under different environmental conditions and can be considered as ecoparalogs.


Subject(s)
Archaeal Proteins/metabolism , Flagellin/metabolism , Genes, Archaeal , Haloarcula marismortui/genetics , Archaeal Proteins/chemistry , Archaeal Proteins/genetics , Flagellin/chemistry , Flagellin/genetics , Haloarcula marismortui/metabolism , Hot Temperature , Protein Stability , Protein Structure, Tertiary , Salt Tolerance
10.
Can J Microbiol ; 54(10): 835-44, 2008 Oct.
Article in English | MEDLINE | ID: mdl-18923552

ABSTRACT

Many Archaea use rotation of helical flagellar filaments for swimming motility. We isolated and characterized the flagellar filaments of Haloarcula marismortui, an archaeal species previously considered to be nonmotile. Two Haloarcula marismortui phenotypes were discriminated--their filaments are composed predominantly of either FlaB or FlaA2 flagellin, and the corresponding genes are located on different replicons. FlaB and FlaA2 filaments differ in antigenicity and thermostability. FlaA2 filaments are distinctly thicker (20-22 nm) than FlaB filaments (16-18 nm). The observed filaments are nearly twice as thick as those of other characterized euryarchaeal filaments. The results suggest that the helicity of Haloarcula marismortui filaments is provided by a mechanism different from that in the related haloarchaeon Halobacterium salinarum, where 2 different flagellin molecules present in comparable quantities are required to form a helical filament.


Subject(s)
Archaeal Proteins/metabolism , Chlorides/metabolism , Flagella/metabolism , Flagellin/metabolism , Haloarcula marismortui/metabolism , Amino Acid Sequence , Archaeal Proteins/chemistry , Archaeal Proteins/genetics , Flagella/chemistry , Flagella/genetics , Flagellin/chemistry , Flagellin/genetics , Haloarcula marismortui/chemistry , Haloarcula marismortui/genetics , Molecular Sequence Data , Sequence Alignment
11.
FEMS Microbiol Lett ; 212(1): 23-7, 2002 Jun 18.
Article in English | MEDLINE | ID: mdl-12076782

ABSTRACT

We examine distribution of flagellins along multicomponent flagellar filaments (FF) and protofilaments (PF) of the haloalkaliphilic archaeon Natrialba magadii using immunogold electron microscopy. A high specific polyclonal antibody raised to one of the flagellin types bound homogeneously to the undissociated FF along the full length. At the same time both uniformly labelled and completely unlabelled PF, outwardly indistinguishable one from another, were observed.


Subject(s)
Flagella/immunology , Flagella/ultrastructure , Flagellin/metabolism , Halobacteriaceae/metabolism , Electrophoresis, Polyacrylamide Gel , Flagellin/immunology , Halobacteriaceae/immunology , Halobacteriaceae/ultrastructure , Microscopy, Immunoelectron
12.
Extremophiles ; 6(2): 135-42, 2002 Apr.
Article in English | MEDLINE | ID: mdl-12013434

ABSTRACT

Nucleoside diphosphate kinase from the haloalkaliphilic archaeon Natrialba magadii (Nm NDPK) is a homooligomeric hexamer with a monomer molecular weight of 23 kDa. Its main function is to exchange gamma-phosphates between nucleoside triphosphates and diphosphates. Previously it was shown that Nm NDPK is active over a wide range of NaCl concentrations, which is not typical of extremely halophilic proteins. In this paper more detailed investigations of kinase function and stability were carried out using circular dichroism, differential scanning calorimetry, size-exclusion chromatography, and biochemical methods. A possible mechanism for stabilization of halophilic proteins that allows them to function in a wide range of NaCl concentrations is proposed.


Subject(s)
Halobacteriaceae/enzymology , Nucleoside-Diphosphate Kinase/chemistry , Nucleoside-Diphosphate Kinase/metabolism , Amino Acids/analysis , Archaeal Proteins/chemistry , Archaeal Proteins/metabolism , Calorimetry, Differential Scanning , Circular Dichroism , Enzyme Stability , Molecular Weight , Protein Structure, Quaternary , Protein Structure, Secondary , Protein Structure, Tertiary , Sodium Chloride , Spectrometry, Fluorescence , Temperature
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