General methods for identification of carotenoids.

Abstract:

:General methods for identification of usual carotenoids including C18-HPLC retention time and spectroscopic methods, such as absorption spectra, mass spectra, NMR spectra, are briefly summarized.

journal_name

Biotechnol Lett

journal_title

Biotechnology letters

authors

Takaichi S

doi

10.1007/s10529-014-1479-4

subject

Has Abstract

pub_date

2014-06-01 00:00:00

pages

1127-8

issue

6

eissn

0141-5492

issn

1573-6776

journal_volume

36

pub_type

信件
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  • Isolation, purification and characterization of a pH tolerant and temperature stable proteinaceous protease inhibitor from marine Pseudomonas mendocina.

    abstract:OBJECTIVES:An extracellular protease inhibitor (BTPI-301) of trypsin was purified and characterized from an isolate of Pseudomonas mendocina. RESULTS:BTPI-301was purified to homogeneity by (NH4)2SO4, precipitation, DEAE Sepharose and CNBr-activated Sepharose chromatography. Homogeneity was proved by native PAGE and SD...

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    authors: Kaneko H,Minagawa H,Shimada J

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    journal_title:Biotechnology letters

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    doi:10.1007/s10529-009-0192-1

    authors: Dehestani A,Kazemitabar K,Ahmadian G,Jelodar NB,Salmanian AH,Seyedi M,Rahimian H,Ghasemi S

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  • Purification and some properties of an extracellular ribonuclease with antiviral activity against tobacco mosaic virus from Bacillus cereus.

    abstract::A new ribonuclease (RNase) with tobacco mosaic virus inhibition was isolated and purified from Bacillus cereus ZH14 through ammonium sulfate precipitation, ultrafiltration, ion-exchange chromatography of DEAE-Sephadex A-50 column, and gel chromatography of Sephacryl S-200HR column. The enzyme was purified approximatel...

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    abstract::We truncated the VP2 protein of infectious bursal disease virus into five fragments: V1-5. All fragments were displayed on the inner membrane of the Escherichia coli periplasm. After disruption of the outer membrane, spheroplasts that had anchored with the VP2 fragment were incubated with an anti-VP2 polyclonal antibo...

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    abstract:OBJECTIVES:The action modes of an endocellulase, EGA, and its domains (CD9 and CBM3) during enzymatic treatment of cotton fabrics were investigated. RESULTS:EGA, CD9 and CBM3 had the binding capacity to cellulose substrates, of which the filter paper was the substrate with the strongest binding capacity. Analyses of s...

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    pub_type: 杂志文章

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    authors: Panić M,Delač D,Roje M,Radojčić Redovniković I,Cvjetko Bubalo M

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    doi:10.1007/s10529-005-6721-7

    authors: Takada M,Nomura N,Okada H,Nakajima-Kambe T,Nakahara T,Uchiyama H

    更新日期:2005-06-01 00:00:00

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    abstract::The volumetric productivity of the beer fermentation process can be increased by using a higher pitching rate (i.e. higher inoculum size). However, the decreased yeast net growth observed in these high cell density brewery fermentations can adversely affect the physiological stability throughout subsequent yeast gener...

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    pub_type: 杂志文章

    doi:10.1007/s10529-009-0067-5

    authors: Verbelen PJ,Dekoninck TM,Van Mulders SE,Saerens SM,Delvaux F,Delvaux FR

    更新日期:2009-11-01 00:00:00

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    abstract::Many enzymes used as digestive aids exhibit, at best, moderate stability when incubated under gastrointestinal conditions. A supplemental β-galactosidase administered orally to treat lactose intolerance was conjugated to 40 kDa, branched polyethylene glycol (PEG). PEGylation increased the enzyme's relative activity at...

    journal_title:Biotechnology letters

    pub_type: 杂志文章

    doi:10.1007/s10529-010-0474-7

    authors: Turner KM,Pasut G,Veronese FM,Boyce A,Walsh G

    更新日期:2011-03-01 00:00:00

  • Identification of genes controlled by the manganese response regulator, ManR, in the cyanobacterium, Anabaena sp. PCC 7120.

    abstract::A computational search was carried out to identify additional binding sites for the manganese response regulator, ManR, in the genome of Anabaena sp. PCC 7120. This approach predicted ManR binding sites: the promoter regions of the genes of all3575-alr3576 and the gene of alr5134 from Anabaena sp. PCC 7120. Electropho...

    journal_title:Biotechnology letters

    pub_type: 杂志文章

    doi:10.1023/B:BILE.0000045639.26579.6f

    authors: Huang W,Wu QY

    更新日期:2004-09-01 00:00:00

  • The tandem affinity purification technology: an overview.

    abstract::Tandem affinity purification (TAP) is a methodology for the isolation of protein complexes from endogenous sources. It involves incorporation of a dual-affinity tag into the protein of interest and introduction of the construct into desired cell lines or organisms. Using the two affinity handles, the protein complex a...

    journal_title:Biotechnology letters

    pub_type: 杂志文章,评审

    doi:10.1007/s10529-011-0592-x

    authors: Li Y

    更新日期:2011-08-01 00:00:00