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t benhamiae strain ihem 20161  (ATCC)


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    Structured Review

    ATCC t benhamiae strain ihem 20161
    T Benhamiae Strain Ihem 20161, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 84 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/20161/Fusarium+falciforme%3B+Strain%3A+Fu3/pm39980131-27-1-11
    Average 95 stars, based on 84 article reviews
    t benhamiae strain ihem 20161 - by Bioz Stars, 2026-09
    95/100 stars

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    Related Articles

    other:

    Article Title: Fermentation of acidic-pretreated glycerol for enhanced 1,3-PDO production by immobilized Clostridium butyricum JKT 37 on coconut shell activated carbon
    Article Snippet: Rodriguez A, Wojtusik M, Ripoll V, Santos VE, Garcia-Ochoa F (2016) 1, 3-Propanediol production from glycerol with a novel biocatalyst Shimwellia blattae ATCC 33430: operational conditions and kinetics in batch cultivations.

    Marker:

    Article Title: Gut microbiome in tumorigenesis and therapy of colorectal cancer.
    Article Snippet: Shenzhen Branch, Guangdong Laboratory for Lingnan Modern Agriculture, Genome Analysis Laboratory of the Ministry of Agriculture, Agricultural Genomics Institute at Shenzhen, Chinese Academy of Agricultural Sciences, Shenzhen, People's Republic of China Hubei Hongshan Laboratory, College of Biomedicine and Health, Huazhong Agricultural University, Wuhan, People's Republic of China Hubei Key Laboratory of Agricultural Bioinformatics, College of Life Science and Technology, Interdisciplinary Sciences Institute, Huazhong Agricultural University, Wuhan, People's Republic of China Shenzhen Institute of Nutrition and Health, Huazhong Agricultural University, Shenzhen, People's Republic of China

    Bacteria:

    Article Title: Gut microbiome in tumorigenesis and therapy of colorectal cancer.
    Article Snippet: Shenzhen Branch, Guangdong Laboratory for Lingnan Modern Agriculture, Genome Analysis Laboratory of the Ministry of Agriculture, Agricultural Genomics Institute at Shenzhen, Chinese Academy of Agricultural Sciences, Shenzhen, People's Republic of China Hubei Hongshan Laboratory, College of Biomedicine and Health, Huazhong Agricultural University, Wuhan, People's Republic of China Hubei Key Laboratory of Agricultural Bioinformatics, College of Life Science and Technology, Interdisciplinary Sciences Institute, Huazhong Agricultural University, Wuhan, People's Republic of China Shenzhen Institute of Nutrition and Health, Huazhong Agricultural University, Shenzhen, People's Republic of China

    Article Title: Genomic insight into iron acquisition by sulfate-reducing bacteria in microaerophilic environments.
    Article Snippet: Sulfate-reducing bacteria (SRB) are broadly distributed throughout the biosphere and are an ecological and physiological group of microorganisms known for anaerobic growth, performing dissimilatory reduction of sulfates (Widdel et al. 2007).. However, although commonly referred to as obligate anaerobes, SRB have systems to prevent cell death when exposed to O2 (Barton and Fauque 2022).. SRB grow at the oxicanoxic interface in waste water biofilms (Santegoeds et al. 1998; Okabe et al. 2005), microbial mats (Canfield and Des Marais, 1991; Krekeler et al. 1997; Teske et al. 1998; Minz et al. 1999), lake sediments (Sass et al. 1997), marine environments and sediments (Jørgensen and Bak 1991; Teske et al. 1996), in marine intertidal zones (Smith et al. 2019), on the surface and inside cells of plant roots (Küsel et al. 1995; Blaabjerg Abstract Historically, sulfate-reducing bacteria (SRB) have been considered to be strict anaerobes, but reports in the past couple of decades indicate that SRB tolerate exposure to O2 and can even grow in aerophilic environments.

    Probiotics:

    Article Title: Gut microbiome in tumorigenesis and therapy of colorectal cancer.
    Article Snippet: Shenzhen Branch, Guangdong Laboratory for Lingnan Modern Agriculture, Genome Analysis Laboratory of the Ministry of Agriculture, Agricultural Genomics Institute at Shenzhen, Chinese Academy of Agricultural Sciences, Shenzhen, People's Republic of China Hubei Hongshan Laboratory, College of Biomedicine and Health, Huazhong Agricultural University, Wuhan, People's Republic of China Hubei Key Laboratory of Agricultural Bioinformatics, College of Life Science and Technology, Interdisciplinary Sciences Institute, Huazhong Agricultural University, Wuhan, People's Republic of China Shenzhen Institute of Nutrition and Health, Huazhong Agricultural University, Shenzhen, People's Republic of China

    In Vitro:

    Article Title: Gut microbiome in tumorigenesis and therapy of colorectal cancer.
    Article Snippet: Shenzhen Branch, Guangdong Laboratory for Lingnan Modern Agriculture, Genome Analysis Laboratory of the Ministry of Agriculture, Agricultural Genomics Institute at Shenzhen, Chinese Academy of Agricultural Sciences, Shenzhen, People's Republic of China Hubei Hongshan Laboratory, College of Biomedicine and Health, Huazhong Agricultural University, Wuhan, People's Republic of China Hubei Key Laboratory of Agricultural Bioinformatics, College of Life Science and Technology, Interdisciplinary Sciences Institute, Huazhong Agricultural University, Wuhan, People's Republic of China Shenzhen Institute of Nutrition and Health, Huazhong Agricultural University, Shenzhen, People's Republic of China

    Activity Assay:

    Article Title: Gut microbiome in tumorigenesis and therapy of colorectal cancer.
    Article Snippet: Shenzhen Branch, Guangdong Laboratory for Lingnan Modern Agriculture, Genome Analysis Laboratory of the Ministry of Agriculture, Agricultural Genomics Institute at Shenzhen, Chinese Academy of Agricultural Sciences, Shenzhen, People's Republic of China Hubei Hongshan Laboratory, College of Biomedicine and Health, Huazhong Agricultural University, Wuhan, People's Republic of China Hubei Key Laboratory of Agricultural Bioinformatics, College of Life Science and Technology, Interdisciplinary Sciences Institute, Huazhong Agricultural University, Wuhan, People's Republic of China Shenzhen Institute of Nutrition and Health, Huazhong Agricultural University, Shenzhen, People's Republic of China

    Isolation:

    Article Title: Subtilisin 6 From the Dermatophyte Trichophyton benhamiae Is a Marker of Infection but Not a Unique Virulence Factor.
    Article Snippet: Background: Trichophyton benhamiae is a common dermatophyte whose natural host is the guinea pig and which causes highly inflammatory skin lesions in humans.. The subtilisin 6 (SUB6) of this fungus belongs to a family of 12 SUB genes.. Its encoding gene, overexpressed in vivo but not in vitro, has been considered a potentially important virulence factor, but its role in pathogenesis remains to be elucidated.

    Adhesive:

    Article Title: Promise of Combining Antifungal Agents in Denture Adhesives to Fight Candida Species Infections.
    Article Snippet: Lactoferricin B and SMAP28 were active against both C. albicans ATCC 64124 and HMV4C in water, but had anti-C. albicans activities outside the range of concentrations used in our assays in 1% denture adhesive (p < 0.05, Table 1). .. 4 Journal of Prosthodontics 00 (2016) 1–8 C© 2016 by the American College of Prosthodontists Sphingosine, dihydrosphingosine, and phytosphingosine were also active against C. albicans ATCC 64124 and HMV4C in water, but had anti-C. albicans activities outside the range of concentrations used in our assays in 1% denture adhesive (p < 0.05, Table 1). .. The MBCs of sphingosine for C. albicans ATCC 64124 and the MBCs of sphingosine, dihydrosphingosine, and phytosphingosine for C. albicans HMV4C were all lower in water than that in 1% denture adhesive (p < 0.05, Table 1).



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    Image Search Results


    (A)-(B) All constructs tested were described previously (5). The amino acid position of the recombination site of each construct was indicated above the construct. The red line indicates a mutated amino acid position. The domain swap constructs were fused with the C-terminal tag 3xHA, and AvrRp1-D.1 was fused with the C-terminal tag 4xcMYC. The strength of HR resulting from co-expression in N . benthamiana is shown. 9 individual plants were infiltrated and showed similar results. The table to the right indicates the relative strength of the HR induced by the co-expression of AvrRp1-D.1 with each Rp1 chimera or mutant (+++ is the strongest HR). Rp1-D21 was used as a positive control. (C) Yeast two-hybrid assay using strains co-expressing Rp1-D, -dp2, -dp6, and -dp7 fused to the GAL4 activation domain (AD) with AvrRp1-D.1 fused to the GAL4 DNA binding domain (BD) on control media lacking leucine and tryptophan (-LW) or selective media additionally lacking histidine (-LWH). Growth on selective media indicates protein-protein interactions. Interaction between T antigen with GAL4 activation domain and Lam or p53 with GAL4 DNA binding domain were used as negative/positive control, respectively. AD- or BD-binding proteins were detected using anti-GAL4 and anti-GAL4 (DBD). (D) Schematic diagram of the parts into which Rp1-D was divided for the yeast-two-hybrid assay shown in (E). (E) Yeast two-hybrid assay using strains co-expressing each part of Rp1-D or Rp1-dp7 shown in the schematic above fused to AD with AvrRp1-D.1 or Lam fused to BD on control media lacking leucine and tryptophan (-LW) or selective media additionally lacking histidine (-LWH). Pictures were taken 5 days after plating.

    Journal: PLOS Pathogens

    Article Title: Use of the Puccinia sorghi haustorial transcriptome to identify and characterize AvrRp1-D recognized by the maize Rp1-D resistance protein

    doi: 10.1371/journal.ppat.1012662

    Figure Lengend Snippet: (A)-(B) All constructs tested were described previously (5). The amino acid position of the recombination site of each construct was indicated above the construct. The red line indicates a mutated amino acid position. The domain swap constructs were fused with the C-terminal tag 3xHA, and AvrRp1-D.1 was fused with the C-terminal tag 4xcMYC. The strength of HR resulting from co-expression in N . benthamiana is shown. 9 individual plants were infiltrated and showed similar results. The table to the right indicates the relative strength of the HR induced by the co-expression of AvrRp1-D.1 with each Rp1 chimera or mutant (+++ is the strongest HR). Rp1-D21 was used as a positive control. (C) Yeast two-hybrid assay using strains co-expressing Rp1-D, -dp2, -dp6, and -dp7 fused to the GAL4 activation domain (AD) with AvrRp1-D.1 fused to the GAL4 DNA binding domain (BD) on control media lacking leucine and tryptophan (-LW) or selective media additionally lacking histidine (-LWH). Growth on selective media indicates protein-protein interactions. Interaction between T antigen with GAL4 activation domain and Lam or p53 with GAL4 DNA binding domain were used as negative/positive control, respectively. AD- or BD-binding proteins were detected using anti-GAL4 and anti-GAL4 (DBD). (D) Schematic diagram of the parts into which Rp1-D was divided for the yeast-two-hybrid assay shown in (E). (E) Yeast two-hybrid assay using strains co-expressing each part of Rp1-D or Rp1-dp7 shown in the schematic above fused to AD with AvrRp1-D.1 or Lam fused to BD on control media lacking leucine and tryptophan (-LW) or selective media additionally lacking histidine (-LWH). Pictures were taken 5 days after plating.

    Article Snippet: To generate a yeast expression vector with Rp1 alleles, their deletion constructs, and effector, Rp1 alleles and their deletion constructs were cloned into a yeast expression vector containing GAL4 activation domain (addgene #20161), and the effector gene was cloned the vector containing GAL4 binding domain (addgene #20162).

    Techniques: Construct, Expressing, Mutagenesis, Positive Control, Y2H Assay, Activation Assay, Binding Assay, Control, Protein-Protein interactions