{"title":"Spontaneous formation, gene regulation of Trichoderma and slow decomposition in cocopeat","authors":"Avinash Sharma , Mainu Hazarika , Punabati Heisnam , Himanshu Pandey , V.S. Devadas , Praveen Kumar , Devendra Singh , Amit Vashishth , Monoj Sutradhar , Rani Jha","doi":"10.1016/j.nxsust.2024.100051","DOIUrl":null,"url":null,"abstract":"<div><p>Cocopeat has various distinguishing properties that encourage the slow decomposition and spontaneous <em>Trichoderma</em> growth. The cocopeat synthesizes responsive chemicals and regulatory mechanisms which assist in the <em>Trichoderma</em> growth. The exact chemical stimulant and efficient mechanisms governing the spontaneous <em>Trichoderma</em> growth in cocopeat remain unknown. The high lignin and cellulose concentration produces actinomycetes and deuteromycetes, which trigger slow decomposition in cocopeat. The chemical components, temperature, pH, nutrients, and aeration all have a direct impact <em>Trichoderma</em> growth and slow decomposition. The chemical constituents lignin, suberin, cutin, pectin, cellulose, and hemicellulose are analyzed with sodium hydroxide solution and examined using scanning electron microscopy (SEM), energy dispersive x-ray spectroscopy (EDAX), fourier transform infrared (FTIR) spectra, x-ray diffraction (XRD), and thermogravimetry. The decomposition dynamics are determined using a mettler thermogravimetric analyzer. Simultaneously thermogravimetry and differential scanning calorimetry are used to examine the stages of decomposition. The decomposition reactions are investigated using the distributed active energy model (DAEM). The glucose Murashige and Skoog (MS) media, chitin Murashige and Skoog (MS) media, Murashige and Skoog (MS) basal media, high-density oligonucleotide microarray, expressed sequence tag-based transcript and Blast2GO suite, hierarchical clustering and heat representation are involved in examination of <em>Trichoderma</em> species. The Upside regulating genes respond to signal transduction, transcription, translation, post-translational modification, and protein folding with the signal transcription factor Pac1 (PacC) for <em>Trichoderma</em> species growth. The dye decolorization assay, genome-wide gene family evolutionary analysis, and whole-genome sequencing were used to discover prospective genes for detecting high or slow decomposition in fungi. The methodologies and technology have the potential to investigate <em>Trichoderma</em> type, response chemicals, and mechanisms underlying <em>Trichoderma</em> growth and slow decomposition in cocopeat.</p></div>","PeriodicalId":100960,"journal":{"name":"Next Sustainability","volume":"4 ","pages":"Article 100051"},"PeriodicalIF":0.0000,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S294982362400028X/pdfft?md5=2459b0b65ac6efc08de4aa3a532dad6e&pid=1-s2.0-S294982362400028X-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Next Sustainability","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S294982362400028X","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Cocopeat has various distinguishing properties that encourage the slow decomposition and spontaneous Trichoderma growth. The cocopeat synthesizes responsive chemicals and regulatory mechanisms which assist in the Trichoderma growth. The exact chemical stimulant and efficient mechanisms governing the spontaneous Trichoderma growth in cocopeat remain unknown. The high lignin and cellulose concentration produces actinomycetes and deuteromycetes, which trigger slow decomposition in cocopeat. The chemical components, temperature, pH, nutrients, and aeration all have a direct impact Trichoderma growth and slow decomposition. The chemical constituents lignin, suberin, cutin, pectin, cellulose, and hemicellulose are analyzed with sodium hydroxide solution and examined using scanning electron microscopy (SEM), energy dispersive x-ray spectroscopy (EDAX), fourier transform infrared (FTIR) spectra, x-ray diffraction (XRD), and thermogravimetry. The decomposition dynamics are determined using a mettler thermogravimetric analyzer. Simultaneously thermogravimetry and differential scanning calorimetry are used to examine the stages of decomposition. The decomposition reactions are investigated using the distributed active energy model (DAEM). The glucose Murashige and Skoog (MS) media, chitin Murashige and Skoog (MS) media, Murashige and Skoog (MS) basal media, high-density oligonucleotide microarray, expressed sequence tag-based transcript and Blast2GO suite, hierarchical clustering and heat representation are involved in examination of Trichoderma species. The Upside regulating genes respond to signal transduction, transcription, translation, post-translational modification, and protein folding with the signal transcription factor Pac1 (PacC) for Trichoderma species growth. The dye decolorization assay, genome-wide gene family evolutionary analysis, and whole-genome sequencing were used to discover prospective genes for detecting high or slow decomposition in fungi. The methodologies and technology have the potential to investigate Trichoderma type, response chemicals, and mechanisms underlying Trichoderma growth and slow decomposition in cocopeat.