10 research outputs found
Single Chirality Extraction of Single-Wall Carbon Nanotubes for the Encapsulation of Organic Molecules
The hollow inner spaces of single-wall carbon nanotubes
(SWCNTs)
can confine various types of molecules. Many remarkable phenomena
have been observed inside SWCNTs while encapsulating organic molecules
(peapods). However, a mixed electronic structure state of the surrounding
SWCNTs has impeded a detailed understanding of the physical/chemical
properties of peapods and their device applications. We present a
single-chirality purification method for SWCNTs that can encapsulate
organic molecules. A single-chiral state of (11,10) SWCNTs with a
diameter of 1.44 nm, which is large enough for molecular encapsulation,
was obtained after a two-step purification method: metal-semiconductor
sorting and cesium-chloride sorting. The encapsulation of C<sub>60</sub> to the (11,10) SWCNTs was also succeeded, promising a route toward
single-chirality peapod devices
Cocrystal or Salt Crystallization for Active Pharmaceutical Ingredients By Using Deep Eutectic Solvents
Active pharmaceutical ingredients (APIs) often exhibit
physicochemical
problems that one can remedy by various methods (e.g., salt formation,
grinding, ordered mixtures, and cocrystal or amorphous formation).
Crystallizing salts or cocrystals from solutions of an API and a coformer
is widely used today. In recent years, green chemistry and sustainable
development goals have been an active area of research, and a production
method is required for reducing the use of organic solvents and implementing
a low environmental load. In this study, deep eutectic solvents (DESs)
were used as the mother liquids for crystallization and environmentally
friendly solvents. The DESs were made by combining three types of
choline salts and a coformer compound of malonic acid. Nine model
APIs were then dissolved in each DES and crystals precipitated from
the DESs. As a result, five kinds of cocrystals or salts precipitated
in 10 conditions, two of which were identified for the first time
in this study. Crystallization by using DESs is a potent alternative
for discovering novel cocrystals or salts with low environmental impact
Spectroscopic Characterization of Nanohybrids Consisting of Single-walled Carbon Nanotubes and Fullerodendron
<div><p>Hydrogen gas, which can be used in fuel cells to generate electricity, is considered the ultimate clean energy source. Recently, it was reported that a photo-induced electron transfer system consisting of single-walled carbon nanotubes (SWCNTs) and fullerodendrons shows photo-catalytic activity with a very high quantum yield for splitting water under visible light irradiation. However, the mechanism of high efficiency hydrogen generation is not yet clearly understood. We report here the spectroscopic characterizations of the SWCNT-fullerodendron composites. The results indicate two important fundamental properties of the composite system. First, fullerodendrons preferentially interact with the semiconducting SWCNTs instead of with their metallic counterparts. Second, the photo-induced electron transfer process from the C<sub>60</sub> moiety of fullerodendrons to SWCNTs occurs more efficiently with an increasing tube diameter.</p>
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Biochemical Characterization of UDP-<i>N</i>-acetylmuramoyl-L-alanyl-D-glutamate: <i>meso</i>-2,6-diaminopimelate ligase (MurE) from <i>Verrucomicrobium spinosum</i> DSM 4136<sup>T</sup>
<div><p><i>Verrucomicrobium spinosum</i> is a Gram-negative bacterium that is related to bacteria from the genus <i>Chlamydia</i>. The bacterium is pathogenic towards <i>Drosophila melanogaster</i> and <i>Caenorhabditis elegans</i>, using a type III secretion system to facilitate pathogenicity. <i>V. spinosum</i> employs the recently discovered l,l-diaminopimelate aminotransferase biosynthetic pathway to generate the bacterial cell wall and protein precursors diaminopimelate and lysine. A survey of the <i>V. spinosum</i> genome provides evidence that the bacterium should be able to synthesize peptidoglycan <i>de novo</i>, since all of the necessary genes are present. The enzyme UDP-<i>N</i>-acetylmuramoyl-l-alanyl-d-glutamate: <i>meso</i>-2,6-diaminopimelate ligase (MurE) (E.C. 6.3.2.15) catalyzes a reaction in the cytoplasmic step of peptidoglycan biosynthesis by adding the third amino acid residue to the peptide stem. The <i>murE</i> ortholog from <i>V. spinosum</i> (<i>murE</i><sub>Vs</sub>) was cloned and was shown to possess UDP-MurNAc-l-Ala-d-Glu:<i>meso</i>-2,6-diaminopimelate ligase activity <i>in vivo</i> using functional complementation. <i>In vitro</i> analysis using the purified recombinant enzyme demonstrated that MurE<sub>Vs</sub> has a pH optimum of 9.6 and a magnesium optimum of 30 mM. <i>meso</i>-Diaminopimelate was the preferred substrate with a <i>K</i><sub>m</sub> of 17 µM, when compared to other substrates that are structurally related. Sequence alignment and structural analysis using homology modeling suggest that key residues that make up the active site of the enzyme are conserved in MurE<sub>Vs</sub>. Our kinetic analysis and structural model of MurE<sub>Vs</sub> is consistent with other MurE enzymes from Gram-negative bacteria that have been characterized. To verify that <i>V. spinosum</i> incorporates diaminopimelate into its cell wall, we purified peptidoglycan from a <i>V. spinosum</i> culture; analysis revealed the presence of diaminopimelate, consistent with that of a bona fide peptidoglycan from Gram-negative bacteria.</p></div
The monomer unit of the peptidoglycan structure.
<p>The disaccharide moiety is composed of the amino sugars <i>N</i>-acetylglucosamine (GlcNAc) and <i>N</i>-acetylmuramic (MurNAc) linked via a β-1,4 glycosidic bond. The amino acid at position 3 of the stem peptide is <i>meso</i>-diaminopimelic acid (R =  COOH) in most Gram-negative bacteria and l-lysine (R = H) in most Gram-positive bacteria.</p
Homolgy model of MurE<sub>Vs</sub>.
<p>(a) The homology model of MurE<sub>Vs</sub> highlighting domains A (grey), B (violet) and C (pink). (b) Shows the structure model of MurE<sub>Vs</sub> bound to UDP-MurNAc-tripeptide (UMT) product (yellow). (c) Active site residue hypothesized to bind to UMT product is shown in red. The structure has been rotated 90° on the right panel for the better viewing of the binding pocket. (d) Cross eye stereo view showing the interaction between amino acid residues of the binding site and UMT product.</p
Expression and purification of recombinant MurE<sub>Vs</sub> using His-tag affinity chromatography.
<p>Lane (1) protein makers (kDa); Lane (2) 10 µg of soluble protein from uninduced cells; Lane (3) 10 µg of soluble protein from induced cells; Lane (4) 1 µg of purified recombinant MurE<sub>Vs</sub>. The proteins were resolved on 10% (w/v) acrylamide gel and were stained using Coomassie blue.</p
Analysis of crude and purified PG from <i>V. spinosum</i> DSM 4136<sup>T</sup>.
a<p>Crude and purified PG designate the macromolecule before and after, respectively, treatment with pancreatin, pronase and trypsin (see Materials and Methods).</p
List of genes involved in PG metabolism of <i>V. spinosum</i> DSM 4136<sup>T</sup>.
<p>The annotated gene product names are from NCBI (<a href="http://www.ncbi.nlm.nih.gov/protein/" target="_blank">www.ncbi.nlm.nih.gov/protein/</a>) queried of February 28, 2013. The pencillin-binding proteins (PBP) class designations are denoted by activity based on <b><u>p</u></b>rotein <b><u>fam</u></b>ily (pfam) domains. Class A and class B PBPs are high-molecular mass PBPs while class C PBPs are low-molecular mass PBPs. Class A PBPs are predicted to have both transglycosylase and transpeptidase activities; class B PBPs are predicted to have only transpeptidase activity; class C PBPs are predicted to have d,d-carboxypeptidase activity.</p
Multiple amino acid sequence alignment of five representative sequences of MurE.
<p>The residues that are predicted to be involved in binding in the active site are marked with a star below the sequence. The sequence identity score against MurE from <i>V. spinosum</i> was: <i>C. trachomatis,</i> 37%; <i>E. coli,</i> 35%; <i>P. carotovorum</i>, 36%; and <i>M. tuberculosis</i>. The multiple amino acid sequence alignment figure was generated using the ESPript 2.2 server (<a href="http://espript.ibcp.fr/ESPript/cgi-bin/ESPript.cgi" target="_blank">http://espript.ibcp.fr/ESPript/cgi-bin/ESPript.cgi</a>).</p