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Fungal diversity in adult date palm(Phoenix dactylifera L.) revealed by culture-dependent and culture-independent approaches

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Journal of Zhejiang University-Science B(Biomedicine & Biotechnology) 2013年第12期14卷 1084-1099页

作者： Ines BEN CHOBBA Amine ELLEUCH Imen AYADI Lamia KHANNOUS Ahmed NAMSI Frederique CERQUEIRA Noureddine DRIRA Néji GHARSALLAH tatiana vallaeys Laboratoire de Biotechnologies Végétales Appliquées à l'Amélioration des Cultures LBVAAC Faculté des Sciences de SfaxB.P. 1171 3000 Sfax Tunisia UMR 5119 Université de Montpellier 2 Sciences et Techniques pl E. BataillonCC093 34095 Montpellier France Laboratoire de Microorganismes et de Biomolécules Centre de Biotechnologie de Sfax Université de Sfax Route Sidi MansourB.P. 1177 3018 Sfax Tunisia Laboratoire de Phytopathologie Oasienne Centre Régional de Recherches en Agriculture Oasienne à DegacheDegache 2260 Tunisia Plateforme Séquen age-Génotypage SFR "Montpellier Environnement Biodiversité" ISEM Université de Montpellier 234095 Montpellier France

Endophytic flora plays a vital role in the colonization and survival of host plants, especially in harsh environments, such as arid regions. This flora may, however, contain pathogenic species responsible for various troublesome host diseases. The present study is aimed at investigating the diversity of both cultivable and non-cultivable endophytic fungal floras in the internal tissues(roots and leaves) of Tunisian date palm trees(Phoenix dactylifera). Accordingly, 13 isolates from both root and leaf samples, exhibiting distinct colony morphology, were selected from potato dextrose agar(PDA) medium and identified by a sequence match search wherein their 18S–28S internal transcribed spacer(ITS) sequences were compared to those available in public databases. These findings revealed that the cultivable root and leaf isolates fell into two groups, namely Nectriaceae and Pleosporaceae. Additionally, total DNA from palm roots and leaves was further extracted and ITS fragments were amplified. Restriction fragment length polymorphism(RFLP) analysis of the ITS from 200 fungal clones(leaves: 100; roots: 100) using HaeIII restriction enzyme revealed 13 distinct patterns that were further sequenced and led to the identification of Alternaria, Cladosporium, Davidiella(Cladosporium teleomorph), Pythium, Curvularia, and uncharacterized fungal endophytes. Both approaches confirmed that while the roots were predominantly colonized by Fusaria(members of the Nectriaceae family), the leaves were essentially colonized by Alternaria(members of the Pleosporaceae family). Overall, the findings of the present study constitute, to the authors' knowledge, the first extensive report on the diversity of endophytic fungal flora associated with date palm trees(P. dactylifera).

关键词： Date palm tree(Phoenix dactylifera) Endophytic cultivable fungi rDNA internal transcribed spacer(ITS) Phylogenetic analysis Total DNA diversity analysis

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<i>Arthrobacter arilaitensis</i>Re117 as a Source of Solvent-Stable Proteases: Production, Characteristics, Potential Application in the Deproteinization of Shrimp Wastes and Evaluation in Liquid Laundry Commercial Detergents

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Advances in Bioscience and Biotechnology 2015年第2期6卷 105-119页

作者： Rayda Siala Ines Hammemi Sabrine Sellimi tatiana vallaeys Alya Sellami Kamoun Moncef Nasri Laboratory of Enzyme Engineering and Microbiology National School of Engineering of Sfax (ENIS) University of Sfax Sfax Tunisia Unité de Recherche Protection des Plantes Cultivées et Environnement Institut de l’Olivier Sfax Tunisia Laboratoire Ecosystèmes Lagunaires UMR 5119 Université de Montpellier Montpellier France

The present study describes the characterization of crude protease extract from Arthrobacter arilaitensis Re117 and its evaluation in solid and liquid detergent. One caseinolytic protease clear band was observed in zymogram. The crude alkaline protease showed optimum activity at pH 9.0 and 50°C, and it was highly stable over a wide range of pH from 8.0 to 9.0. Proteolytic enzymes showed extreme stability towards non-ionic surfactants (Tween 80, Tween 20 and Triton X-100) and stimulate activity towards oxidizing agents such as sodium perborate. They also showed high stability and compatibility with various laundry solid detergents from Tunisian market. The protease of A. arilaitensis Re117, was also tested for shrimp waste deproteinization to produce chitin. The protein removal with a ratio E/S of 20 was about 83%. The novelties of the Re117 protease include its high stability to organic solvents and surfactants. These unique properties make it an ideal choice for application in detergent formulations and enzymatic peptide synthesis. In addition, the enzyme may find potential applications in the deproteinization of shrimp wastes to produce chitin.

关键词： A. arilaitensis Shrimp Wastes Enzymatic Deproteinization Organic Solvent-Stable Protease Laundry Detergents Compatibility

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