scholarly journals Studies on Vascular Infection of Fusarium oxysporum f. sp. cubense Race 4 in Banana by Field Survey and Green Fluorescent Protein Reporter

2013 ◽  
Vol 2 (1) ◽  
pp. 44-51 ◽  
Author(s):  
Rong F. Xiao ◽  
Yu-Jing Zhu ◽  
Yan-Dan Li ◽  
Bo Liu
Keyword(s):  
Green Fluorescent Protein ◽  
Fusarium Oxysporum ◽  
Field Survey ◽  
Fluorescent Protein ◽  
Infection Process ◽  
Gene Encoding ◽  
Effective Prevention ◽  
Green Fluorescent ◽  
Banana Wilt ◽  
Race 4

Fusarium wilt of banana (Musa spp.) caused by Fusarium oxysporum f. sp. cubense (Foc) is one of the most serious banana fungal diseases in the world. Understanding the infection process of Foc is important for development of effective ways in disease control. In order to follow infection and colonization of this pathogen from root to rhizome and pseudostem tissues of banana, a highly pathogenic strain FJAT-3076 of Foc race 4 (Foc4) was transformed with gene encoding green fluorescent protein (GFP) and the fungus carrying gfp (FJAT-3076-GFP) was used to inoculate banana plants (Cavendish cv. B.F.). After inoculation for 3 to 10 d, it was observed that the conidia and their germ-tubes had penetrated into epidermis of young roots. The hyphae were found inside the root xylem 10 d after inoculation in the rhizome and pseudostem xylem after inoculation for 17 d. All plants infected by Foc died in 24 d after inoculation. It was also observed that Foc had spread all over the xylem and part of hyphae reached the pseudostem surface. Hyphal population was found the highest in the pseudostem, lower in root and least in rhizome. Field survey confirmed that Foc4 were mostly present in the base of pseudostem and less in the rhizome. Thus, effective prevention of the Foc hyphae movement from the rhizome up to the pseudostem might delay or control banana wilt disease.

scholarly journals Microplate Bioassay for Nisin in Foods, Based on Nisin-Induced Green Fluorescent Protein Fluorescence

2003 ◽  
Vol 69 (7) ◽  
pp. 4214-4218 ◽  
Author(s):  
J. Reunanen ◽  
P. E. J. Saris
Keyword(s):  
Green Fluorescent Protein ◽  
Lactococcus Lactis ◽  
Culture Supernatant ◽  
Fluorescent Protein ◽  
Green Fluorescent Protein Fluorescence ◽  
Regulatory Proteins ◽  
Protein Fluorescence ◽  
Gene Encoding ◽  
Two Component ◽  
Green Fluorescent

ABSTRACT A plasmid coding for the nisin two-component regulatory proteins, NisK and NisR, was constructed; in this plasmid a gfp gene (encoding the green fluorescent protein) was placed under control of the nisin-inducible nisF promoter. The plasmid was transformed into non-nisin-producing Lactococcus lactis strain MG1614. The new strain could sense extracellular nisin and transduce it to green fluorescent protein fluorescence. The amount of fluorescence was dependent on the nisin concentration, and it could be measured easily. By using this strain, an assay for quantification of nisin was developed. With this method it was possible to measure as little as 2.5 ng of pure nisin per ml in culture supernatant, 45 ng of nisin per ml in milk, 0.9 μg of nisin in cheese, and 1 μg of nisin per ml in salad dressings.

scholarly journals Identification and Characterization of a Novel Gene Involved in the trans-Specific Nematicidal Activity of Photorhabdus luminescens LN2

2009 ◽  
Vol 75 (12) ◽  
pp. 4221-4223 ◽  
Author(s):  
Xuehong Qiu ◽  
Richou Han ◽  
Xun Yan ◽  
Mingxing Liu ◽  
Li Cao ◽  
...  
Keyword(s):  
Green Fluorescent Protein ◽  
Fluorescent Protein ◽  
Transposon Mutagenesis ◽  
Nematicidal Activity ◽  
Photorhabdus Luminescens ◽  
Gene Encoding ◽  
Heterorhabditis Indica ◽  
Green Fluorescent ◽  
Identification And Characterization

ABSTRACT Photorhabdus luminescens subsp. akhurstii LN2 from Heterorhabditis indica LN2 showed nematicidal activity against axenic Heterorhabditis bacteriophora H06 infective juveniles (IJs). Transposon mutagenesis identified an LN2 mutant that supports the growth of H06 nematodes. Tn5 disrupted the namA gene, encoding a novel 364-residue protein and involving the nematicidal activity. The green fluorescent protein-labeled namA mutant was unable to colonize the intestines of H06 IJs.

Colonization of Fusarium Wilt-Resistant and Susceptible Watermelon Roots by a Green-Fluorescent-Protein-tagged Isolate of Fusarium oxysporum f.sp. niveum

2013 ◽  
Vol 162 (4) ◽  
pp. 228-237 ◽  
Author(s):  
Guiyun Lü ◽  
Shaogui Guo ◽  
Haiying Zhang ◽  
Lihua Geng ◽  
Raymond D. Martyn ◽  
...  
Keyword(s):  
Green Fluorescent Protein ◽  
Fusarium Oxysporum ◽  
Fusarium Wilt ◽  
Fluorescent Protein ◽  
Green Fluorescent

scholarly journals Use of green fluorescent protein to monitor fungal growth in biomass hydrolysate

2018 ◽  
Vol 3 (1) ◽  
Author(s):  
Nancy N Nichols ◽  
Joshua C Quarterman ◽  
Sarah E Frazer
Keyword(s):  
Green Fluorescent Protein ◽  
Fluorescent Protein ◽  
Fungal Growth ◽  
Fermentation Inhibitors ◽  
Gene Encoding ◽  
Agricultural Residue ◽  
Biomass Hydrolysate ◽  
Physico Chemical ◽  
Colony Forming Units ◽  
Green Fluorescent

Abstract A reporter gene encoding green fluorescent protein (GFP) was introduced into the ascomycete Coniochaeta ligniaria NRRL30616, and fluorescence of cultures was monitored as a measure of cell growth. Fluorescence in the GFP-expressing strain was measured during growth of cells in defined and complex media as well as in the liquor derived from pretreatment of corn stover, an agricultural residue. Fluorescence mirrored growth of cultures, as measured by optical density and counts of colony forming units. Because traditional methods to monitor growth cannot be used in biomass liquors due to its fibrous, dark-colored nature, the speed and convenience of using GFP to monitor growth is advantageous. Fluorescence of cultures in biomass hydrolysate also correlated with the concentration of furfural in hydrolysate. Furfural and other compounds, present in hydrolysate due to physico-chemical pretreatment of biomass, are inhibitory to fermenting microbes. Therefore, measurement of fluorescence in GFP-expressing C. ligniaria is a proxy for measures of microbial growth and furfural consumption, and serves as a convenient indicator of metabolism of fermentation inhibitors in biomass hydrolysate.

scholarly journals Replication-Competent Rhabdoviruses with Human Immunodeficiency Virus Type 1 Coats and Green Fluorescent Protein: Entry by a pH-Independent Pathway

1999 ◽  
Vol 73 (8) ◽  
pp. 6937-6945 ◽  
Author(s):  
Eli Boritz ◽  
Jennifer Gerlach ◽  
J. Erik Johnson ◽  
John K. Rose
Keyword(s):  
Human Immunodeficiency Virus ◽  
Green Fluorescent Protein ◽  
Human Immunodeficiency Virus Type ◽  
Virus Type ◽  
Neutralizing Antibodies ◽  
Fluorescent Protein ◽  
Gene Encoding ◽  
Immunodeficiency Virus ◽  
Green Fluorescent

ABSTRACT We describe a replication-competent, recombinant vesicular stomatitis virus (VSV) in which the gene encoding the single transmembrane glycoprotein (G) was deleted and replaced by anenv-G hybrid gene encoding the extracellular and transmembrane domains of a human immunodeficiency virus type 1 (HIV-1) envelope protein fused to the cytoplasmic domain of VSV G. An additional gene encoding a green fluorescent protein was added to permit rapid detection of infection. This novel surrogate virus infected and propagated on cells expressing the HIV receptor CD4 and coreceptor CXCR4. Infection was blocked by SDF-1, the ligand for CXCR4, by antibody to CD4 and by HIV-neutralizing antibody. This virus, unlike VSV, entered cells by a pH-independent pathway and thus supports a pH-independent pathway of HIV entry. Additional recombinants carrying hybrid env-G genes derived from R5 or X4R5 HIV strains also showed the coreceptor specificities of the HIV strains from which they were derived. These surrogate viruses provide a simple and rapid assay for HIV-neutralizing antibodies as well as a rapid screen for molecules that would interfere with any stage of HIV binding or entry. The viruses might also be useful as HIV vaccines. Our results suggest wide applications of other surrogate viruses based on VSV.

Use of Green Fluorescent Protein To Detect Expression of an Endopolygalacturonase Gene of Colletotrichum lindemuthianum during Bean Infection

1999 ◽  
Vol 65 (4) ◽  
pp. 1769-1771 ◽  
Author(s):  
Bernard Dumas ◽  
Sylvie Centis ◽  
Nathalie Sarrazin ◽  
Marie-Thérèse Esquerré-Tugayé
Keyword(s):  
Green Fluorescent Protein ◽  
Fluorescence Microscopy ◽  
Fluorescent Protein ◽  
Colletotrichum Lindemuthianum ◽  
Fungal Genome ◽  
Appressorium Formation ◽  
Gene Encoding ◽  
Green Fluorescent ◽  
Microscopy Examination

ABSTRACT The 5′ noncoding region of clpg2, an endopolygalacturonase gene of the bean pathogenColletotrichum lindemuthianum, was fused to the coding sequence of a gene encoding a green fluorescent protein (GFP), and the construct was introduced into the fungal genome. Detection of GFP accumulation by fluorescence microscopy examination revealed thatclpg2 was expressed at the early stages of germination of the conidia and during appressorium formation both in vitro and on the host plant.

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