alternaria alternata Search Results


alternaria alternata fries keissler  (ATCC)
92
ATCC alternaria alternata fries keissler
Impact of application with an edible coating based on nanochitosan (NCt) and its composite with rosmarinic acid/Se nanoparticles (NCt/RA/SeNPs) on the growth of <t> Alternaria </t> <t> alternata, </t> in vitro and on experimentally infected persimmon fruits after 21 days of storage at 15 °C.
Alternaria Alternata Fries Keissler, supplied by ATCC, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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a alternata  (DSMZ)
92
DSMZ a alternata
Fig. 6. Pathogen-induced expression of the GUS reporter gene under the control of different derivatives of the AtWRKY33 promoter. A, Schematic diagram of the 5′ upstream region of the AtWRKY33 gene. Bent arrows marked with P1 to P6 represent the different 5′ ends of the AtWRKY33 promoter used to generate transgenic Arabidopsis AtWRKY33::GUS expres- sion lines. The transcription start site is marked with +1, and the first exon indicated. Putative W box DNA elements are boxed and those relevant for this publication are marked W1 to W4. B, Histochemical GUS activity staining in leaves of different AtWRKY33promoter::GUS transgenic reporter lines challenged with Alternaria brassicicola or A. <t>alternata</t> (mid two leaves in b, AtWRKY33-P1::GUS lines). Fungal suspension was applied (25- to 50-µl droplets per leaf) and staining performed 5 and 6 days postinocu- lation. Representative leaves from both T2 and T3 transgenic lines har- boring the indicated AtWRKY33::GUS reporter constructs are shown. Three independent repetitions, each using leaves from several transgenic lines, were performed.
A Alternata, supplied by DSMZ, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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lactobacillus reuteri  (ATCC)
93
ATCC lactobacillus reuteri
Fig. 6. Pathogen-induced expression of the GUS reporter gene under the control of different derivatives of the AtWRKY33 promoter. A, Schematic diagram of the 5′ upstream region of the AtWRKY33 gene. Bent arrows marked with P1 to P6 represent the different 5′ ends of the AtWRKY33 promoter used to generate transgenic Arabidopsis AtWRKY33::GUS expres- sion lines. The transcription start site is marked with +1, and the first exon indicated. Putative W box DNA elements are boxed and those relevant for this publication are marked W1 to W4. B, Histochemical GUS activity staining in leaves of different AtWRKY33promoter::GUS transgenic reporter lines challenged with Alternaria brassicicola or A. <t>alternata</t> (mid two leaves in b, AtWRKY33-P1::GUS lines). Fungal suspension was applied (25- to 50-µl droplets per leaf) and staining performed 5 and 6 days postinocu- lation. Representative leaves from both T2 and T3 transgenic lines har- boring the indicated AtWRKY33::GUS reporter constructs are shown. Three independent repetitions, each using leaves from several transgenic lines, were performed.
Lactobacillus Reuteri, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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alternaria alternata  (ATCC)
95
ATCC alternaria alternata
Fig. 6. Pathogen-induced expression of the GUS reporter gene under the control of different derivatives of the AtWRKY33 promoter. A, Schematic diagram of the 5′ upstream region of the AtWRKY33 gene. Bent arrows marked with P1 to P6 represent the different 5′ ends of the AtWRKY33 promoter used to generate transgenic Arabidopsis AtWRKY33::GUS expres- sion lines. The transcription start site is marked with +1, and the first exon indicated. Putative W box DNA elements are boxed and those relevant for this publication are marked W1 to W4. B, Histochemical GUS activity staining in leaves of different AtWRKY33promoter::GUS transgenic reporter lines challenged with Alternaria brassicicola or A. <t>alternata</t> (mid two leaves in b, AtWRKY33-P1::GUS lines). Fungal suspension was applied (25- to 50-µl droplets per leaf) and staining performed 5 and 6 days postinocu- lation. Representative leaves from both T2 and T3 transgenic lines har- boring the indicated AtWRKY33::GUS reporter constructs are shown. Three independent repetitions, each using leaves from several transgenic lines, were performed.
Alternaria Alternata, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/alternaria+alternata/Alternaria+alternata/pm30799037-252-14-16
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alternaria alternata strain atcc 13963  (ATCC)
94
ATCC alternaria alternata strain atcc 13963
Fig. 6. Pathogen-induced expression of the GUS reporter gene under the control of different derivatives of the AtWRKY33 promoter. A, Schematic diagram of the 5′ upstream region of the AtWRKY33 gene. Bent arrows marked with P1 to P6 represent the different 5′ ends of the AtWRKY33 promoter used to generate transgenic Arabidopsis AtWRKY33::GUS expres- sion lines. The transcription start site is marked with +1, and the first exon indicated. Putative W box DNA elements are boxed and those relevant for this publication are marked W1 to W4. B, Histochemical GUS activity staining in leaves of different AtWRKY33promoter::GUS transgenic reporter lines challenged with Alternaria brassicicola or A. <t>alternata</t> (mid two leaves in b, AtWRKY33-P1::GUS lines). Fungal suspension was applied (25- to 50-µl droplets per leaf) and staining performed 5 and 6 days postinocu- lation. Representative leaves from both T2 and T3 transgenic lines har- boring the indicated AtWRKY33::GUS reporter constructs are shown. Three independent repetitions, each using leaves from several transgenic lines, were performed.
Alternaria Alternata Strain Atcc 13963, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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b subtilis atcc 6663  (ATCC)
93
ATCC b subtilis atcc 6663
Fig. 6. Pathogen-induced expression of the GUS reporter gene under the control of different derivatives of the AtWRKY33 promoter. A, Schematic diagram of the 5′ upstream region of the AtWRKY33 gene. Bent arrows marked with P1 to P6 represent the different 5′ ends of the AtWRKY33 promoter used to generate transgenic Arabidopsis AtWRKY33::GUS expres- sion lines. The transcription start site is marked with +1, and the first exon indicated. Putative W box DNA elements are boxed and those relevant for this publication are marked W1 to W4. B, Histochemical GUS activity staining in leaves of different AtWRKY33promoter::GUS transgenic reporter lines challenged with Alternaria brassicicola or A. <t>alternata</t> (mid two leaves in b, AtWRKY33-P1::GUS lines). Fungal suspension was applied (25- to 50-µl droplets per leaf) and staining performed 5 and 6 days postinocu- lation. Representative leaves from both T2 and T3 transgenic lines har- boring the indicated AtWRKY33::GUS reporter constructs are shown. Three independent repetitions, each using leaves from several transgenic lines, were performed.
B Subtilis Atcc 6663, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/alternaria+alternata/Alternaria+alternata/pmc12488318-258-3-5
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culture derived alternaria alternata  (ATCC)
94
ATCC culture derived alternaria alternata
Fig. 6. Pathogen-induced expression of the GUS reporter gene under the control of different derivatives of the AtWRKY33 promoter. A, Schematic diagram of the 5′ upstream region of the AtWRKY33 gene. Bent arrows marked with P1 to P6 represent the different 5′ ends of the AtWRKY33 promoter used to generate transgenic Arabidopsis AtWRKY33::GUS expres- sion lines. The transcription start site is marked with +1, and the first exon indicated. Putative W box DNA elements are boxed and those relevant for this publication are marked W1 to W4. B, Histochemical GUS activity staining in leaves of different AtWRKY33promoter::GUS transgenic reporter lines challenged with Alternaria brassicicola or A. <t>alternata</t> (mid two leaves in b, AtWRKY33-P1::GUS lines). Fungal suspension was applied (25- to 50-µl droplets per leaf) and staining performed 5 and 6 days postinocu- lation. Representative leaves from both T2 and T3 transgenic lines har- boring the indicated AtWRKY33::GUS reporter constructs are shown. Three independent repetitions, each using leaves from several transgenic lines, were performed.
Culture Derived Alternaria Alternata, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/alternaria+alternata/Alternaria+alternata+(Fries)+Keissler/pmc02872482-95-30-33
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4642 hq263343 kj817328 medium method b  (ATCC)
93
ATCC 4642 hq263343 kj817328 medium method b
Fig. 6. Pathogen-induced expression of the GUS reporter gene under the control of different derivatives of the AtWRKY33 promoter. A, Schematic diagram of the 5′ upstream region of the AtWRKY33 gene. Bent arrows marked with P1 to P6 represent the different 5′ ends of the AtWRKY33 promoter used to generate transgenic Arabidopsis AtWRKY33::GUS expres- sion lines. The transcription start site is marked with +1, and the first exon indicated. Putative W box DNA elements are boxed and those relevant for this publication are marked W1 to W4. B, Histochemical GUS activity staining in leaves of different AtWRKY33promoter::GUS transgenic reporter lines challenged with Alternaria brassicicola or A. <t>alternata</t> (mid two leaves in b, AtWRKY33-P1::GUS lines). Fungal suspension was applied (25- to 50-µl droplets per leaf) and staining performed 5 and 6 days postinocu- lation. Representative leaves from both T2 and T3 transgenic lines har- boring the indicated AtWRKY33::GUS reporter constructs are shown. Three independent repetitions, each using leaves from several transgenic lines, were performed.
4642 Hq263343 Kj817328 Medium Method B, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/alternaria+alternata/Alternaria+alternata+(Fries)+Keissler/pmc06165096__antibiotics___07___00083___s001-122-159-158
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Image Search Results


Impact of application with an edible coating based on nanochitosan (NCt) and its composite with rosmarinic acid/Se nanoparticles (NCt/RA/SeNPs) on the growth of Alternaria alternata, in vitro and on experimentally infected persimmon fruits after 21 days of storage at 15 °C.

Journal: Polymers

Article Title: Innovative Approach for Controlling Black Rot of Persimmon Fruits by Means of Nanobiotechnology from Nanochitosan and Rosmarinic Acid-Mediated Selenium Nanoparticles

doi: 10.3390/polym14102116

Figure Lengend Snippet: Impact of application with an edible coating based on nanochitosan (NCt) and its composite with rosmarinic acid/Se nanoparticles (NCt/RA/SeNPs) on the growth of Alternaria alternata, in vitro and on experimentally infected persimmon fruits after 21 days of storage at 15 °C.

Article Snippet: Alternaria alternata (Fries) Keissler (ATCC-44498) was employed to assess the antifungal potentiality of synthesized nanoparticles/nanocomposites.

Techniques: In Vitro, Infection

Fig. 6. Pathogen-induced expression of the GUS reporter gene under the control of different derivatives of the AtWRKY33 promoter. A, Schematic diagram of the 5′ upstream region of the AtWRKY33 gene. Bent arrows marked with P1 to P6 represent the different 5′ ends of the AtWRKY33 promoter used to generate transgenic Arabidopsis AtWRKY33::GUS expres- sion lines. The transcription start site is marked with +1, and the first exon indicated. Putative W box DNA elements are boxed and those relevant for this publication are marked W1 to W4. B, Histochemical GUS activity staining in leaves of different AtWRKY33promoter::GUS transgenic reporter lines challenged with Alternaria brassicicola or A. alternata (mid two leaves in b, AtWRKY33-P1::GUS lines). Fungal suspension was applied (25- to 50-µl droplets per leaf) and staining performed 5 and 6 days postinocu- lation. Representative leaves from both T2 and T3 transgenic lines har- boring the indicated AtWRKY33::GUS reporter constructs are shown. Three independent repetitions, each using leaves from several transgenic lines, were performed.

Journal: Molecular Plant-Microbe Interactions®

Article Title: Expression ofAtWRKY33Encoding a Pathogen- or PAMP-Responsive WRKY Transcription Factor Is Regulated by a Composite DNA Motif Containing W Box Elements

doi: 10.1094/mpmi-20-4-0420

Figure Lengend Snippet: Fig. 6. Pathogen-induced expression of the GUS reporter gene under the control of different derivatives of the AtWRKY33 promoter. A, Schematic diagram of the 5′ upstream region of the AtWRKY33 gene. Bent arrows marked with P1 to P6 represent the different 5′ ends of the AtWRKY33 promoter used to generate transgenic Arabidopsis AtWRKY33::GUS expres- sion lines. The transcription start site is marked with +1, and the first exon indicated. Putative W box DNA elements are boxed and those relevant for this publication are marked W1 to W4. B, Histochemical GUS activity staining in leaves of different AtWRKY33promoter::GUS transgenic reporter lines challenged with Alternaria brassicicola or A. alternata (mid two leaves in b, AtWRKY33-P1::GUS lines). Fungal suspension was applied (25- to 50-µl droplets per leaf) and staining performed 5 and 6 days postinocu- lation. Representative leaves from both T2 and T3 transgenic lines har- boring the indicated AtWRKY33::GUS reporter constructs are shown. Three independent repetitions, each using leaves from several transgenic lines, were performed.

Article Snippet: A. alternata and Pythium sylvaticum were obtained from DSMZ, the German National Resource Centre for Biological Material (Braunschweig, Germany), and S. sclerotiorum was kindly provided by W. Gieffers (MPIZ).

Techniques: Expressing, Control, Transgenic Assay, Activity Assay, Staining, Suspension, Construct