Preparation of antibacterial microfibre

Three different kinds of antibacterial microfibres (270D, 300D and 330D) have been developed by adding 2-4 wt % nano silver masterbatch in the melt spinning process. The mechanical properties, silver content and morphology have been examined with tensile tester, inductively coupled plasma-optical emission spectrometer and scanning electron microscope respectively. Their antibacterial abilities are also studied with KS K 0693:2011. The results show that the added nano-particles have little influence on mechanical properties of antibacterial microfibres and their max strain and tenacity are similar to that of common manmade fibre. The fineness of the 270D, 300D and 330D samples are found to be 0.23, 0.26 and 0.30 den, and the corresponding added silver contents are 265.5, 231 and 259 ppm respectively. It is also observed that all samples bacteriostatic reduction rates are about 99.9% for both Staphylococcus aureus and Klebsiella pneumonia before washing. But after washing, it drops to 65.4%/75%, 91.9%/97.7% and 94.8%/99.9% respectively for both the bacteria in case of 270D, 300D and 330D samples. It is concluded that 300D and 330D microfibre samples have good antibacterial ability before and after washing

Preparation of antibacterial microfibre

145-149<span style="font-size:11.0pt;mso-bidi-font-size: 10.0pt;font-family:" times="" new="" roman";mso-fareast-font-family:"times="" roman";="" mso-bidi-font-family:"times="" roman";mso-ansi-language:en-gb;mso-fareast-language:="" en-us;mso-bidi-language:ar-sa"="" lang="EN-GB">Three different kinds of antibacterial microfibres (270D, 300D and 330D) have been developed by adding 2-4 wt % nano silver masterbatch in the melt spinning process. The mechanical properties, silver content and morphology have been examined <span style="font-size:11.0pt;mso-bidi-font-size:10.0pt; font-family:" times="" new="" roman";mso-fareast-font-family:pmingliu;mso-bidi-font-family:="" "times="" roman";mso-ansi-language:en-gb;mso-fareast-language:zh-tw;="" mso-bidi-language:ar-sa"="" lang="EN-GB">with<span style="font-size:11.0pt; mso-bidi-font-size:10.0pt;font-family:" times="" new="" roman";mso-fareast-font-family:="" "times="" roman";mso-bidi-font-family:"times="" roman";mso-ansi-language:="" en-gb;mso-fareast-language:en-us;mso-bidi-language:ar-sa"="" lang="EN-GB"> tensile tester, inductively coupled plasma-optical emission spectrometer and scanning electron microscope respectively. <span style="font-size: 11.0pt;mso-bidi-font-size:10.0pt;font-family:" times="" new="" roman";mso-fareast-font-family:="" pmingliu;mso-bidi-font-family:"times="" roman";mso-ansi-language:en-gb;="" mso-fareast-language:zh-tw;mso-bidi-language:ar-sa"="" lang="EN-GB">Their antibacterial abilit<span style="font-size:11.0pt;mso-bidi-font-size:10.0pt; font-family:" times="" new="" roman";mso-fareast-font-family:pmingliu;mso-bidi-font-family:="" "times="" roman";mso-ansi-language:en-gb;mso-fareast-language:zh-tw;="" mso-bidi-language:ar-sa"="" lang="EN-GB">ies<span style="font-size:11.0pt; mso-bidi-font-size:10.0pt;font-family:" times="" new="" roman";mso-fareast-font-family:="" "times="" roman";mso-bidi-font-family:"times="" roman";mso-ansi-language:="" en-gb;mso-fareast-language:en-us;mso-bidi-language:ar-sa"="" lang="EN-GB"> are also studied with <span style="font-size:11.0pt;mso-bidi-font-size: 10.0pt;font-family:" times="" new="" roman";mso-fareast-font-family:"times="" roman";="" mso-bidi-font-family:"times="" roman";mso-ansi-language:en-gb;mso-fareast-language:="" en-us;mso-bidi-language:ar-sa"="" lang="EN-GB">KS K 0693:2011. The results<span style="font-size:11.0pt;mso-bidi-font-size:10.0pt; font-family:" times="" new="" roman";mso-fareast-font-family:"times="" roman";="" mso-bidi-font-family:"times="" roman";mso-ansi-language:en-gb;mso-fareast-language:="" en-us;mso-bidi-language:ar-sa"="" lang="EN-GB"> show that the added nano-particles have little influence on mechanical properties of antibacterial microfibres and their max strain and tenacity are similar to that of common manmade fibre. The fineness of the 270D, 300D and 330D samples are found to be 0.23, 0.26 and 0.30 den, and the corresponding added silver contents are 265.5, 231 and 259 ppm respectively. It is also observed that all samples bacteriostatic reduction rates are about 99.9% for both Staphylococcus aureus and Klebsiella pneumonia before washing. But after washing, it drops to 65.4%/75%, 91.9%/97.7% and 94.8%/99.9% respectively for both the bacteria in case of 270D, 300D and 330D samples. It is concluded that 300D and 330D microfibre samples have good antibacterial ability before and after washing.</span

Expression and characterization of a human cDNA that complements the temperature-sensitive defect in dolichol kinase activity in the yeast sec59-1 mutant: the enzymatic phosphorylation of dolichol and diacylglycerol are catalyzed by separate CTP-mediated kinase activities in Saccharomyces cerevisiae

Dolichol kinase (DK) catalyzes the CTP-mediated phosphorylation of dolichol in eukaryotic cells, the terminal step in dolichyl monophosphate (Dol-P) biosynthesis de novo. In S. cerevisiae, the SEC59 gene encodes a protein essential for the expression of DK, an enzyme activity that is required for cell viability and normal rates of lipid intermediate synthesis and protein N-glycosylation. This study identifies a cDNA clone from human brain that encodes the mammalian homolog of DK (hDK1p). hDK1 is capable of complementing the growth defect, elevating DK activity, and consequently increasing Dol-P levels in vivo and restoring normal N-glycosylation of carboxypeptidase Y at the restrictive temperature in the temperature-sensitive mutant sec59-1. The CTP-mediated phosphorylation of diacylglycerol (DAG) is unaffected by either the temperature-sensitive mutation in the sec59-1 strain, overexpression of the SEC59 gene, or the mammalian homolog hDK1 under conditions that produced a loss or elevation in the level of DK activity. Additionally, overexpression of hDK1p in Sf-9 cells resulted in a 15-fold increase in DK activity but not DAG kinase activity in crude microsomal fractions. The cloned cDNA contains an open reading frame that would encode a protein with 538 amino acids and a molecular weight of 59,268 kDa. Consistent with this prediction, new polypeptides were detected with an apparent molecular weight of 59-60 kDa when His6-tagged constructs of hDK1 or the SEC59 gene were expressed in Sf-9 cells or the temperature-sensitive sec59-1 mutant cells, respectively. These results identify the first cDNA clone encoding a protein required for the expression of DK activity, possibly the catalytic subunit, in a mammalian cell, and establish that the phosphorylation of dolichol and DAG are catalyzed by separate kinase activities in yeas

Minimizing Freshwater Consumption in the Wash-Off Step in Textile Reactive Dyeing by Catalytic Ozonation with Carbon Aerogel Hosted Bimetallic Catalyst

In textile reactive dyeing, dyed fabrics have to be rinsed in the wash-off step several times to improve colorfastness. Thus, the multiple rinsing processes drastically increase the freshwater consumption and meanwhile generate massive waste rinsing effluents. This paper addresses an innovative alternative to recycle the waste effluents to minimize freshwater consumption in the wash-off step. Accordingly, catalytic ozonation with a highly effective catalyst has been applied to remedy the waste rinsing effluents for recycling. The carbon aerogel (CA) hosted bimetallic hybrid material (Ag–Fe2O3@CA) was fabricated and used as the catalyst in the degradation of residual dyes in the waste rinsing effluents by ozonation treatments. The results indicate the participation of Ag–Fe2O3@CA had strikingly enhanced the removal percentage of chemical oxidation demand by 30%. In addition, it has been validated that waste effluents had been successfully reclaimed after catalytic ozonation with Ag–Fe2O3@CA. They could be additionally reused to reduce freshwater consumption in the wash-off step, but without sacrificing the color quality of corresponding fabrics in terms of color difference and colorfastness. This study may be the first to report the feasibility of catalytic ozonation in minimization of freshwater consumption in the wash-off step in textile reactive dyeing

Expression and characterization of a human cDNA that complements the temperature-sensitive defect in dolichol kinase activity in the yeast sec59-1 mutant: the enzymatic phosphorylation of dolichol and diacylglycerol are catalyzed by separate CTP-mediated kinase activities in Saccharomyces cerevisiae

ISSN:0959-665

Distribution of recombinant UNC50 protein.

<p>Hep3B cells at approximately 40% confluence were transfected with 1 μg pEGFP-N1-UNC50. After 48-hour transfection, cells were fixed in 4% paraformaldehyde and stained for Golgi apparatus, endoplasmic reticulum, and early endosome markers AKR7A2, calnexin 1, and early endosomal autoantigen 1 (EEA1), respectively. Cells were examined under a fluorescence microscope at corresponding excitation light. Scale bar is 10 μm.</p

UNC50 Prompts G1/S Transition and Proliferation in HCC by Regulation of Epidermal Growth Factor Receptor Trafficking

<div><p>Background</p><p>UNC50 has long been recognized as a Golgi apparatus protein in yeast, and is involved in nicotinic receptor trafficking in <i>Caenorhabditis elegans</i>, but little is known about <i>UNC50</i> gene function in human biology despite it being conserved from yeast to high eukaryotes.</p><p>Objectives</p><p>We investigated the relation between UNC50 and human hepatocellular carcinoma (HCC) and the potential mechanisms underlying HCC development.</p><p>Methods</p><p><i>UNC50</i> mRNA expression patterns in 12 HCC and adjacent non-cancerous tissues determined using northern blotting were confirmed by real-time PCR in another 44 paired tissues. Microarray experiments were used to screen for global effects of UNC50 knockdown in the Hep3B cell line, and were confirmed by real-time PCR, western blotting, flow cytometry, and tetrazolium assay in both UNC50 overexpression and knockdown Hep3B cells.</p><p>Results</p><p>UNC50 expression levels were upregulated in HCC tissues in comparison with the adjacent non-cancerous tissues. UNC50 knockdown reduced mRNA levels of the downstream targets of the epidermal growth factor receptor (EGFR) pathway: cyclin D1 (<i>CCND1</i>), <i>EGF</i>, matrix metalloproteinase-7 (<i>MMP7</i>), aldose reductase-like 1 (<i>AKR1B10</i>), cell surface–associated mucin 1 (<i>MUC1</i>), and gastrin (<i>GAST</i>). Moreover, UNC50 influenced EGF, inducing cell cycle entry by affecting cell surface EGFR amounts.</p><p>Conclusions</p><p><i>UNC50</i> may plays some roles in HCC progression by affecting the EGFR pathway.</p></div