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Experimental Investigations on the Effects of Carbon and Nitrogen Sources on Concomitant Amylase and Polygalacturonase Production by Trichoderma viride BITRS-1001 in Submerged Fermentation.

Biotechnology research international

Juwon AD, Emmanuel OF.
PMID: 22919504
Biotechnol Res Int. 2012;2012:904763. doi: 10.1155/2012/904763. Epub 2012 Jul 15.

The paper investigates the effects of different commercial carbon and nitrogen sources on the concomitant synthesis of amylase and polygalacturonase enzymes with the aim of optimizing them for maximal enzyme production. The microorganism used in this work was the...

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Juwon AD, Emmanuel OF. Experimental Investigations on the Effects of Carbon and Nitrogen Sources on Concomitant Amylase and Polygalacturonase Production by Trichoderma viride BITRS-1001 in Submerged Fermentation. Biotechnol Res Int. 2012;2012:904763doi: 10.1155/2012/904763.
Juwon, A. D., & Emmanuel, O. F. (2012). Experimental Investigations on the Effects of Carbon and Nitrogen Sources on Concomitant Amylase and Polygalacturonase Production by Trichoderma viride BITRS-1001 in Submerged Fermentation. Biotechnology research international, 2012904763. https://doi.org/10.1155/2012/904763
Juwon, Arotupin Daniel, and Emmanuel, Ogunmolu Funso. "Experimental Investigations on the Effects of Carbon and Nitrogen Sources on Concomitant Amylase and Polygalacturonase Production by Trichoderma viride BITRS-1001 in Submerged Fermentation." Biotechnology research international vol. 2012 (2012): 904763. doi: https://doi.org/10.1155/2012/904763
Juwon AD, Emmanuel OF. Experimental Investigations on the Effects of Carbon and Nitrogen Sources on Concomitant Amylase and Polygalacturonase Production by Trichoderma viride BITRS-1001 in Submerged Fermentation. Biotechnol Res Int. 2012;2012:904763. doi: 10.1155/2012/904763. Epub 2012 Jul 15. PMID: 22919504; PMCID: PMC3418636.
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Retting and degumming of natural fibers by pectinolytic enzymes produced from Bacillus tequilensis SV11-UV37 using solid state fermentation.

SpringerPlus

Chiliveri SR, Koti S, Linga VR.
PMID: 27218009
Springerplus. 2016 May 04;5:559. doi: 10.1186/s40064-016-2173-x. eCollection 2016.

The present study demonstrated the simultaneous production and optimization of pectinolytic enzymes (pectate lyase and polygalacturonase) under SSF from Bacillus tequilensis SV11-UV37 using wheat bran as a substrate, which is commercially viable and cost-effective. Optimization by one variable-at-a-time-approach showed...

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Chiliveri SR, Koti S, Linga VR. Retting and degumming of natural fibers by pectinolytic enzymes produced from Bacillus tequilensis SV11-UV37 using solid state fermentation. Springerplus. 2016;5:559doi: 10.1186/s40064-016-2173-x.
Chiliveri, S. R., Koti, S., & Linga, V. R. (2016). Retting and degumming of natural fibers by pectinolytic enzymes produced from Bacillus tequilensis SV11-UV37 using solid state fermentation. SpringerPlus, 5559. https://doi.org/10.1186/s40064-016-2173-x
Chiliveri, Swarupa Rani, et al. "Retting and degumming of natural fibers by pectinolytic enzymes produced from Bacillus tequilensis SV11-UV37 using solid state fermentation." SpringerPlus vol. 5 (2016): 559. doi: https://doi.org/10.1186/s40064-016-2173-x
Chiliveri SR, Koti S, Linga VR. Retting and degumming of natural fibers by pectinolytic enzymes produced from Bacillus tequilensis SV11-UV37 using solid state fermentation. Springerplus. 2016 May 04;5:559. doi: 10.1186/s40064-016-2173-x. eCollection 2016. PMID: 27218009; PMCID: PMC4854858.
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Cladosporium cladosporioides from the perspectives of medical and biotechnological approaches.

3 Biotech

AlMatar M, Makky EA.
PMID: 28330073
3 Biotech. 2016 Jun;6(1):4. doi: 10.1007/s13205-015-0323-4. Epub 2015 Dec 31.

Fungi are important natural product sources that have enormous potential for the production of novel compounds for use in pharmacology, agricultural applications and industry. Compared with other natural sources such as plants, fungi are highly diverse but understudied. However,...

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AlMatar M, Makky EA. Cladosporium cladosporioides from the perspectives of medical and biotechnological approaches. 3 Biotech. 2015;6(1):4doi: 10.1007/s13205-015-0323-4.
AlMatar, M., & Makky, E. A. (2016). Cladosporium cladosporioides from the perspectives of medical and biotechnological approaches. 3 Biotech, 6(1), 4. https://doi.org/10.1007/s13205-015-0323-4
AlMatar, Manaf, and Makky, Essam A. "Cladosporium cladosporioides from the perspectives of medical and biotechnological approaches." 3 Biotech vol. 6,1 (2016): 4. doi: https://doi.org/10.1007/s13205-015-0323-4
AlMatar M, Makky EA. Cladosporium cladosporioides from the perspectives of medical and biotechnological approaches. 3 Biotech. 2016 Jun;6(1):4. doi: 10.1007/s13205-015-0323-4. Epub 2015 Dec 31. PMID: 28330073; PMCID: PMC4697913.
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Cytological localization of thePGIP genes in the embryo suspensor cells ofPhaseolus vulgavis L.

TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik

Frediani M, Cremonini R, Salvi G, Caprari C, Desiderio A, D'Ovidio R, Cervone F, De Lorenzo G.
PMID: 24190264
Theor Appl Genet. 1993 Nov;87(3):369-73. doi: 10.1007/BF01184925.

Polygalacturonase-inhibiting protein (PGIP) is a cell wall protein which inhibits fungalendopolygalacturonases. A small gene family encodesPGIP in the genome of common bean, as indicated by Southernblot experiments performed at high-stringency conditions. Southern-blot analysis of DNA extracted from different cultivars...

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Frediani M, Cremonini R, Salvi G, et al. Cytological localization of thePGIP genes in the embryo suspensor cells ofPhaseolus vulgavis L. Theor Appl Genet. 1993;87(3):369-73doi: 10.1007/BF01184925.
Frediani, M., Cremonini, R., Salvi, G., Caprari, C., Desiderio, A., D'Ovidio, R., Cervone, F., & De Lorenzo, G. (1993). Cytological localization of thePGIP genes in the embryo suspensor cells ofPhaseolus vulgavis L. TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik, 87(3), 369-73. https://doi.org/10.1007/BF01184925
Frediani, M, et al. "Cytological localization of thePGIP genes in the embryo suspensor cells ofPhaseolus vulgavis L." TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik vol. 87,3 (1993): 369-73. doi: https://doi.org/10.1007/BF01184925
Frediani M, Cremonini R, Salvi G, Caprari C, Desiderio A, D'Ovidio R, Cervone F, De Lorenzo G. Cytological localization of thePGIP genes in the embryo suspensor cells ofPhaseolus vulgavis L. Theor Appl Genet. 1993 Nov;87(3):369-73. doi: 10.1007/BF01184925. PMID: 24190264.
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Induction of polygalacturonase and the formation of oxalic acid by pectin in brown-rot fungi.

World journal of microbiology & biotechnology

Green F, Clausen CA, Kuster TA, Highley TL.
PMID: 24414906
World J Microbiol Biotechnol. 1995 Sep;11(5):519-24. doi: 10.1007/BF00286366.

Extracellular polygalacturonase (PG) production was estimated in vitro, using liquid cultures of three species of brown-rot decay fungi (Postia placenta, Gloeophyllum trabeum and Serpula incrassata), by cup-plate assay, assay of reducing sugars, and decrease in viscosity. Although all three...

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Green F, Clausen CA, Kuster TA, et al. Induction of polygalacturonase and the formation of oxalic acid by pectin in brown-rot fungi. World J Microbiol Biotechnol. 1995;11(5):519-24doi: 10.1007/BF00286366.
Green, F., Clausen, C. A., Kuster, T. A., & Highley, T. L. (1995). Induction of polygalacturonase and the formation of oxalic acid by pectin in brown-rot fungi. World journal of microbiology & biotechnology, 11(5), 519-24. https://doi.org/10.1007/BF00286366
Green, F, et al. "Induction of polygalacturonase and the formation of oxalic acid by pectin in brown-rot fungi." World journal of microbiology & biotechnology vol. 11,5 (1995): 519-24. doi: https://doi.org/10.1007/BF00286366
Green F, Clausen CA, Kuster TA, Highley TL. Induction of polygalacturonase and the formation of oxalic acid by pectin in brown-rot fungi. World J Microbiol Biotechnol. 1995 Sep;11(5):519-24. doi: 10.1007/BF00286366. PMID: 24414906.
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Detection of polygalacturonases and pectin esterases in lactic acid bacteria.

World journal of microbiology & biotechnology

Karam NE, Belarbi A.
PMID: 24414913
World J Microbiol Biotechnol. 1995 Sep;11(5):559-63. doi: 10.1007/BF00286373.

Of 80 strains of lactic acid bacteria tested, only Lactobacillus casei strains HNK10 and L1-8, Lactobacillus plantarum Lc5 and Lactococcus lactis NN01 produced polygalacturonases (EC 3.2.1.) and/or pectin-esterases (EC 3.1.1.). Crude extracellular extracts of strain L1-8 were able to...

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Karam NE, Belarbi A. Detection of polygalacturonases and pectin esterases in lactic acid bacteria. World J Microbiol Biotechnol. 1995;11(5):559-63doi: 10.1007/BF00286373.
Karam, N. E., & Belarbi, A. (1995). Detection of polygalacturonases and pectin esterases in lactic acid bacteria. World journal of microbiology & biotechnology, 11(5), 559-63. https://doi.org/10.1007/BF00286373
Karam, N E, and Belarbi, A. "Detection of polygalacturonases and pectin esterases in lactic acid bacteria." World journal of microbiology & biotechnology vol. 11,5 (1995): 559-63. doi: https://doi.org/10.1007/BF00286373
Karam NE, Belarbi A. Detection of polygalacturonases and pectin esterases in lactic acid bacteria. World J Microbiol Biotechnol. 1995 Sep;11(5):559-63. doi: 10.1007/BF00286373. PMID: 24414913.
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Tomatine Content in Host and Transgenic Tomatoes by Absorptiometric Measurement.

Bioscience, biotechnology, and biochemistry

Furui H, Inakuma T, Ishiguro Y, Kiso M.
PMID: 27315931
Biosci Biotechnol Biochem. 1998;62(3):556-7. doi: 10.1271/bbb.62.556.

Tomatine is a steroidal glycoalkaloid in tomato plants (Lycopersicon esculentum) and other Lycopersicon and Solanum Species. Tomatine is used as an indicator to evaluate the safety of transgenic tomatoes by FDA in U.S.A. We have developed a facile and...

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Furui H, Inakuma T, Ishiguro Y, et al. Tomatine Content in Host and Transgenic Tomatoes by Absorptiometric Measurement. Biosci Biotechnol Biochem. 1998;62(3):556-7doi: 10.1271/bbb.62.556.
Furui, H., Inakuma, T., Ishiguro, Y., & Kiso, M. (1998). Tomatine Content in Host and Transgenic Tomatoes by Absorptiometric Measurement. Bioscience, biotechnology, and biochemistry, 62(3), 556-7. https://doi.org/10.1271/bbb.62.556
Furui, H, et al. "Tomatine Content in Host and Transgenic Tomatoes by Absorptiometric Measurement." Bioscience, biotechnology, and biochemistry vol. 62,3 (1998): 556-7. doi: https://doi.org/10.1271/bbb.62.556
Furui H, Inakuma T, Ishiguro Y, Kiso M. Tomatine Content in Host and Transgenic Tomatoes by Absorptiometric Measurement. Biosci Biotechnol Biochem. 1998;62(3):556-7. doi: 10.1271/bbb.62.556. PMID: 27315931.
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The Transcription Factor AtDOF4.7 Is Involved in Ethylene- and IDA-Mediated Organ Abscission in Arabidopsis.

Frontiers in plant science

Wang GQ, Wei PC, Tan F, Yu M, Zhang XY, Chen QJ, Wang XC.
PMID: 27379143
Front Plant Sci. 2016 Jun 17;7:863. doi: 10.3389/fpls.2016.00863. eCollection 2016.

Organ abscission is an important plant developmental process that occurs in response to environmental stress or pathogens. In Arabidopsis, ligand signals, such as ethylene or INFLORESCENCE DEFICIENT IN ABSCISSION (IDA), can regulate organ abscission. Previously, we reported that overexpression...

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Wang GQ, Wei PC, Tan F, et al. The Transcription Factor AtDOF4.7 Is Involved in Ethylene- and IDA-Mediated Organ Abscission in Arabidopsis. Front Plant Sci. 2016;7:863doi: 10.3389/fpls.2016.00863.
Wang, G. Q., Wei, P. C., Tan, F., Yu, M., Zhang, X. Y., Chen, Q. J., & Wang, X. C. (2016). The Transcription Factor AtDOF4.7 Is Involved in Ethylene- and IDA-Mediated Organ Abscission in Arabidopsis. Frontiers in plant science, 7863. https://doi.org/10.3389/fpls.2016.00863
Wang, Gao-Qi, et al. "The Transcription Factor AtDOF4.7 Is Involved in Ethylene- and IDA-Mediated Organ Abscission in Arabidopsis." Frontiers in plant science vol. 7 (2016): 863. doi: https://doi.org/10.3389/fpls.2016.00863
Wang GQ, Wei PC, Tan F, Yu M, Zhang XY, Chen QJ, Wang XC. The Transcription Factor AtDOF4.7 Is Involved in Ethylene- and IDA-Mediated Organ Abscission in Arabidopsis. Front Plant Sci. 2016 Jun 17;7:863. doi: 10.3389/fpls.2016.00863. eCollection 2016. PMID: 27379143; PMCID: PMC4911407.
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Extracellular polysaccharidases synthesized by the epiphytic lichen Evernia prunastri (L.) Ach.

Planta

Yagüe E, Orus MI, Estevez MP.
PMID: 24258502
Planta. 1984 Mar;160(3):212-6. doi: 10.1007/BF00402856.

Evernia prunastri Ach., an epiphytic lichen growing on Quercus rotundifolia Lam., produces a β-1,4-glucanase (EC 3.2.1.4) and a polygalacturonase (EC 3.2.1.15). The activity of these polysaccharidases increases as a response to incubation of the lichen with carboxymethylcellulose or sodium...

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Yagüe E, Orus MI, Estevez MP. Extracellular polysaccharidases synthesized by the epiphytic lichen Evernia prunastri (L.) Ach. Planta. 1984;160(3):212-6doi: 10.1007/BF00402856.
Yagüe, E., Orus, M. I., & Estevez, M. P. (1984). Extracellular polysaccharidases synthesized by the epiphytic lichen Evernia prunastri (L.) Ach. Planta, 160(3), 212-6. https://doi.org/10.1007/BF00402856
Yagüe, E, et al. "Extracellular polysaccharidases synthesized by the epiphytic lichen Evernia prunastri (L.) Ach." Planta vol. 160,3 (1984): 212-6. doi: https://doi.org/10.1007/BF00402856
Yagüe E, Orus MI, Estevez MP. Extracellular polysaccharidases synthesized by the epiphytic lichen Evernia prunastri (L.) Ach. Planta. 1984 Mar;160(3):212-6. doi: 10.1007/BF00402856. PMID: 24258502.
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Isolation and characterisation of cDNA clones for tomato polygalacturonase and other ripening-related proteins.

Plant molecular biology

Slater A, Maunders MJ, Edwards K, Schuch W, Grierson D.
PMID: 24306649
Plant Mol Biol. 1985 May;5(3):137-47. doi: 10.1007/BF00015677.

Gene expression during the ripening of tomato fruit was investigated by cDNA cloning and hybrid-select translation. A cDNA library was prepared from poly(A)-containing mRNA from ripe tomato fruit and sreened by differential hybridization. 146 ripening-related cDNA clones were found....

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Slater A, Maunders MJ, Edwards K, et al. Isolation and characterisation of cDNA clones for tomato polygalacturonase and other ripening-related proteins. Plant Mol Biol. 1985;5(3):137-47doi: 10.1007/BF00015677.
Slater, A., Maunders, M. J., Edwards, K., Schuch, W., & Grierson, D. (1985). Isolation and characterisation of cDNA clones for tomato polygalacturonase and other ripening-related proteins. Plant molecular biology, 5(3), 137-47. https://doi.org/10.1007/BF00015677
Slater, A, et al. "Isolation and characterisation of cDNA clones for tomato polygalacturonase and other ripening-related proteins." Plant molecular biology vol. 5,3 (1985): 137-47. doi: https://doi.org/10.1007/BF00015677
Slater A, Maunders MJ, Edwards K, Schuch W, Grierson D. Isolation and characterisation of cDNA clones for tomato polygalacturonase and other ripening-related proteins. Plant Mol Biol. 1985 May;5(3):137-47. doi: 10.1007/BF00015677. PMID: 24306649.
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The tomato polygalacturonase gene and ripening-specific expression in transgenic plants.

Plant molecular biology

Bird CR, Smith CJ, Ray JA, Moureau P, Bevan MW, Bird AS, Hughes S, Morris PC, Grierson D, Schuch W.
PMID: 24272499
Plant Mol Biol. 1988 Sep;11(5):651-62. doi: 10.1007/BF00017465.

Polygalacturonase (PG) is the major cell wall degrading enzyme of tomato fruit. It is developmentally regulated and is synthesised de novo in ripening fruit. Genomic clones encoding a PG gene of tomato (Lycopersicon esculentum Mill cv. Ailsa Craig) have...

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Bird CR, Smith CJ, Ray JA, et al. The tomato polygalacturonase gene and ripening-specific expression in transgenic plants. Plant Mol Biol. 1988;11(5):651-62doi: 10.1007/BF00017465.
Bird, C. R., Smith, C. J., Ray, J. A., Moureau, P., Bevan, M. W., Bird, A. S., Hughes, S., Morris, P. C., Grierson, D., & Schuch, W. (1988). The tomato polygalacturonase gene and ripening-specific expression in transgenic plants. Plant molecular biology, 11(5), 651-62. https://doi.org/10.1007/BF00017465
Bird, C R, et al. "The tomato polygalacturonase gene and ripening-specific expression in transgenic plants." Plant molecular biology vol. 11,5 (1988): 651-62. doi: https://doi.org/10.1007/BF00017465
Bird CR, Smith CJ, Ray JA, Moureau P, Bevan MW, Bird AS, Hughes S, Morris PC, Grierson D, Schuch W. The tomato polygalacturonase gene and ripening-specific expression in transgenic plants. Plant Mol Biol. 1988 Sep;11(5):651-62. doi: 10.1007/BF00017465. PMID: 24272499.
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Comparative genomics of a cannabis pathogen reveals insight into the evolution of pathogenicity in Xanthomonas.

Frontiers in plant science

Jacobs JM, Pesce C, Lefeuvre P, Koebnik R.
PMID: 26136759
Front Plant Sci. 2015 Jun 16;6:431. doi: 10.3389/fpls.2015.00431. eCollection 2015.

Pathogenic bacteria in the genus Xanthomonas cause diseases on over 350 plant species, including cannabis (Cannabis sativa L.). Because of regulatory limitations, the biology of the Xanthomonas-cannabis pathosystem remains largely unexplored. To gain insight into the evolution of Xanthomonas...

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Jacobs JM, Pesce C, Lefeuvre P, et al. Comparative genomics of a cannabis pathogen reveals insight into the evolution of pathogenicity in Xanthomonas. Front Plant Sci. 2015;6:431doi: 10.3389/fpls.2015.00431.
Jacobs, J. M., Pesce, C., Lefeuvre, P., & Koebnik, R. (2015). Comparative genomics of a cannabis pathogen reveals insight into the evolution of pathogenicity in Xanthomonas. Frontiers in plant science, 6431. https://doi.org/10.3389/fpls.2015.00431
Jacobs, Jonathan M, et al. "Comparative genomics of a cannabis pathogen reveals insight into the evolution of pathogenicity in Xanthomonas." Frontiers in plant science vol. 6 (2015): 431. doi: https://doi.org/10.3389/fpls.2015.00431
Jacobs JM, Pesce C, Lefeuvre P, Koebnik R. Comparative genomics of a cannabis pathogen reveals insight into the evolution of pathogenicity in Xanthomonas. Front Plant Sci. 2015 Jun 16;6:431. doi: 10.3389/fpls.2015.00431. eCollection 2015. PMID: 26136759; PMCID: PMC4468381.
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Showing 1 to 12 of 365 entries