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Relevant bibliographies by topics / Chitinase inducing medium

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Journal articles

Academic literature on the topic 'Chitinase inducing medium'

Author: Grafiati

Published: 3 June 2025

Last updated: 31 July 2025

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Journal articles on the topic "Chitinase inducing medium"

1

P., W. H. K. P. Daulagala. "Induction and Expression of Chitinases from Four Sub Species of Bacillus thuringiensis." Journal of Advances in Microbiology 3, no. 1 (2017): 1–8. https://doi.org/10.9734/JAMB/2017/34084.

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Chitin is a naturally occurring linear polymer of <em>N</em>-acetylglucosamine and the major structural component of fungal cell walls and exoskeletons of insects and arthropods. Chitinases are the enzymes that breakdown chitin to economically important derivatives and found in a range of organisms including bacteria, insects, crustaceans, invertebrates, some vertebrates and higher plants. In the present study, four <em>Bacillus thuringiensis </em>(<em>Bt</em>)<em> </em>isolates were grown in media supplemented with 0.1% (w/v) regenerated chitin and chitinase inducing medium and screened for c

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2

Krasnobaeva, I. L., N. M. Kovalenko*, and E. V. Popova. "The effect of chitin on the biological activity of Bacillus subtilis strains." PLANT PROTECTION NEWS 103, no. 4 (2020): 233–40. http://dx.doi.org/10.31993/2308-6459-2020-103-4-13272.

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The aim of the work was to assess the effect of various forms of chitin and chitosan during submerged cultivation of Bacillus subtilis strains, which form the basis of the laboratory sample Vitaplan, CL, on the synthesis of chitinase, as well as on the antagonistic activity and inducing effect of B. subtilis strains in the pathosystems of wheat - Cochliobolus sativus and Puccinia recondita f. sp. tritici. The inclusion of chitin in the form of dry powder or chitin and chitosan in the form of a colloidal suspension into the medium for deep cultivation of bacteria showed that only colloidal chit

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3

Prasad, H. M. Kallesh, J. B. Mythili, Tejaswini ., Lalitha Anand, H. J. Rashmi, and C. Suneetha. "Optimization of Regeneration Protocol and Agrobacterium Mediated Transformation in Carnation (Dianthus caryophyllus L.)." Journal of Horticultural Sciences 4, no. 2 (2009): 120–27. http://dx.doi.org/10.24154/jhs.v4i2.528.

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An efficient and reproducible regeneration protocol for carnation genotypes Arka Flame and IIHRS-1 has been developed from leaf and stem explants. Although IIHRS-1 showed slightly higher regeneration (55%) compared to Arka Flame (49.2%), there was no significant difference in their regeneration response. However, significant difference in regeneration potential was observed with leaf explant exhibiting higher regeneration potential (5.5 shoots/explant) as compared to (4.9) stem explant. Among various plant growth regulator combinations tested for regeneration, the best regeneration response an

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4

Lv, Hang, Shuwu Zhang, Nan Ma, Solomon Boamah, and Bingliang Xu. "Trichoderma longibrachiatum (T6) Peptaibols Inhibiting the Monilia yunnanensis Growth and Inducing Pear Fruit Resistance in Its Infection." Antioxidants 13, no. 12 (2024): 1517. https://doi.org/10.3390/antiox13121517.

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Pear fruit brown rot, caused by Monilia yunnanensis, affects pear fruit yields and quality. The present study determined Trichoderma longibrachiatum T6 (T6) peptaibols as a biological control alternative to synthetic fungicides and assessed its efficacy against M. yunnanensis through dual plate culture and surface spraying at different concentrations. T6 peptaibols effectively inhibited M. yunnanensis growth, achieving an 85.99% inhibitory rate at 1250 µg/mL after inoculation on PDA medium for 5 days, and 84.57% control efficacy on pear fruit with the same concentration at 6 days. Treatment wi

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5

Ma, Liang, Ling Chen, Lei Zhang, et al. "RNA Sequencing Reveals Xyr1 as a Transcription Factor Regulating Gene Expression beyond Carbohydrate Metabolism." BioMed Research International 2016 (2016): 1–20. http://dx.doi.org/10.1155/2016/4841756.

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Xyr1 has been demonstrated to be the main transcription activator of (hemi)cellulases in the well-known cellulase producerTrichoderma reesei. This study comprehensively investigates the genes regulated by Xyr1 through RNA sequencing to produce the transcription profiles ofT. reeseiRut-C30 and itsxyr1deletion mutant (Δxyr1), cultured on lignocellulose or glucose.xyr1deletion resulted in 467 differentially expressed genes on inducing medium. Almost all functional genes involved in (hemi)cellulose degradation and many transporters belonging to the sugar porter family in the major facilitator supe

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6

Meitha, Karlia, Ristag Hanisia, Santiago Signorelli, Tessa Fauziah, Iriawati, and Rizkita Esyanti. "Extracellular DNA of Fusarium oxysporum f. sp. cubense as a Priming Agent for Inducing the Resistance of Banana Plantlets." Agronomy 13, no. 2 (2023): 441. http://dx.doi.org/10.3390/agronomy13020441.

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Fusarium wilt is one of the major causes of global losses in the banana industry. The application of extracellular DNA (eDNA) is explored as a natural fungicide. eDNA is categorized on the basis of the receiving cell’s perception, namely self and non-self. The application of self-eDNA in agriculture presents the potential for limiting the growth of pathogens, while non-self-eDNA, as a vaccine for plants. This study evaluated whether the eDNA from Fusarium oxysporum f. sp. cubense (Foc) could limit the growth of Foc itself (self-inhibition test) while increasing the resistance of banana plant (

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7

SISWANTO, Fetrina OKTAVIA, Asmini BUDIANI, , SUDARSONO, PRIYONO, and Surip MAWARDI. "Transformasi kopi robusta (Coffea canephora) dengan gen kitinase melalui Agrobagterium tumefaciens LBA4404 Transformation of robusta coffee (Coffea canephora) with chitinase gene mediated by Agrobacterium tumefaciens LBA4404." E-Journal Menara Perkebunan 71, no. 2 (2016). http://dx.doi.org/10.22302/iribb.jur.mp.v71i2.162.

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SummaryGenetic engineering of robusta coffee forresistance to pathogenic fungi is considered to beone of the potential approaches to overcome theproblem at robusta coffee plantation caused bypathogenic fungi. This research was aimed tointroduce chitinase (CHI) gene into embryogeniccalli of robusta coffee and regenerate theplantlets. Embryogenic calli were co-cultivatedwith Agrobacterium tumefaciens LBA4404harboring pCAMBIA1301 which containschitinase gene under 35S promoter. In thisresearch four concentrations (0, 50, 100 and150 mg/L) of acetosyringone (AC) were used inthe co-cultivation mediu

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8

SISWANTO, Fetrina OKTAVIA, Asmini BUDIANI, , SUDARSONO, PRIYONO, and Surip MAWARDI. "Transformasi kopi robusta (Coffea canephora) dengan gen kitinase melalui Agrobagterium tumefaciens LBA4404 Transformation of robusta coffee (Coffea canephora) with chitinase gene mediated by Agrobacterium tumefaciens LBA4404." E-Journal Menara Perkebunan 71, no. 2 (2016). http://dx.doi.org/10.22302/ppbbi.jur.mp.v71i2.162.

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Abstract:

SummaryGenetic engineering of robusta coffee forresistance to pathogenic fungi is considered to beone of the potential approaches to overcome theproblem at robusta coffee plantation caused bypathogenic fungi. This research was aimed tointroduce chitinase (CHI) gene into embryogeniccalli of robusta coffee and regenerate theplantlets. Embryogenic calli were co-cultivatedwith Agrobacterium tumefaciens LBA4404harboring pCAMBIA1301 which containschitinase gene under 35S promoter. In thisresearch four concentrations (0, 50, 100 and150 mg/L) of acetosyringone (AC) were used inthe co-cultivation mediu

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