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  1. Article: Impacts of Rhizobium Strain Ar02 on the Nodulation, Growth, Nitrogen (N₂) Fixation Rate and ion Accumulation in Phaseolus vulgaris L. under Salt Stress

    Kouki, Saoussen / L’taief, Boulbaba / Al-Qthanin, Rahamh N. / Sifi, Bouaziz

    Legume research. 2021 Dec., v. 44, no. 12

    2021  

    Abstract: ... on the nodulation, growth, nitrogen (N₂) fixation rate and ion accumulation within Phaseolus vulgaris L. under ...

    Abstract Phaseolus vulgaris L.-rhizobia symbiosis has effectively enhanced common bean productivity via multiple biological mechanisms. This study aims to assess the impacts of the strain of Rhizobium on the nodulation, growth, nitrogen (N₂) fixation rate and ion accumulation within Phaseolus vulgaris L. under salt stress. The Coco Blanc cultivar of the common bean was inoculated with the Ar02 rhizobia strain at 15 days after germination. Bean plants were inoculated in perlite culture to which salt was added in concentrations of 0, 25, 50 and 75 mmol L⁻¹ NaCl. Inoculation with the Ar02 rhizobia strain led to infective and effective symbiosis with the common bean plants exposed to saline solutions and non-saline solutions, respectively. Nodule biomass and nitrogen content declined under salt stress but maintained a higher number of nodules and nodule biomass at 75 mM NaCl. Plant root and shoot length increased with higher biomass under saline conditions, significantly more than the non-inoculated plant without salt. However, the progressive addition of NaCl reduced the growth of the root and shoot and the biomass within the inoculated plant. Salinity led to increased Na+ within the plant’s shoot, along with a reduction in Ca⁺² and K⁺ concentrations. The shoot’s Ca⁺², Na⁺ and K⁺ content were higher in the inoculated plant than the noninoculated. The salt tolerance in common bean plants inoculated with Ar02 rhizobia was linked with the plant’s capability to sustain nodulation and enhance Na+ concentration in the shoot. Furthermore, salt tolerance within the same variety inoculated with Rhizobium was linked to a decline in the Ca⁺ and K⁺ concentrations in the shoot region of salt-exposed plants.
    Keywords Phaseolus vulgaris ; Rhizobium ; beans ; biomass ; cultivars ; germination ; nitrogen ; nitrogen content ; nodulation ; perlite ; research ; roots ; salinity ; salt stress ; salt tolerance ; symbiosis
    Language English
    Dates of publication 2021-12
    Size p. 1529-1533.
    Publishing place Agricultural Research Communication Centre
    Document type Article
    ISSN 0976-0571
    DOI 10.18805/LRF-4716
    Database NAL-Catalogue (AGRICOLA)

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  2. Article ; Online: Synthesis and antiproliferative activity of oxazinocarbazole and N,N-bis(carbazolylmethyl)amine derivatives.

    Issa, Samar / Walchshofer, Nadia / Kassab, Issam / Termoss, Hussein / Chamat, Soulaima / Geahchan, Aziz / Bouaziz, Zouhair

    European journal of medicinal chemistry

    2010  Volume 45, Issue 6, Page(s) 2567–2577

    Abstract: The synthesis, structure elucidation and antitumoral activity of novel heterocyclic compounds containing a carbazole nucleus are reported. Oxazinocarbazoles were synthesized by application of the Mannich reaction to the corresponding hydroxylated ... ...

    Abstract The synthesis, structure elucidation and antitumoral activity of novel heterocyclic compounds containing a carbazole nucleus are reported. Oxazinocarbazoles were synthesized by application of the Mannich reaction to the corresponding hydroxylated derivatives leading to 41 new molecules. Their cytotoxic activity was evaluated against various human tumor cell lines including three leukemic cell lines: CEM and Jurkat (type T), Raji (type B); breast cancer cell line (MCF-7); colorectal cancer cell line (Caco-2). A primary screening at 100 microM allowed the selection of the 10 most active compounds, which showed an antiproliferative activity on all the cell lines. A dose-effect study between 12.5 and 100 microM sorted two compounds with a significant activity: 5t and 7e against leukemic cell lines CEM, Jurkat and Raji with IC50 values around 12 microM.
    MeSH term(s) Amines/chemical synthesis ; Amines/chemistry ; Amines/pharmacology ; Antineoplastic Agents/chemical synthesis ; Antineoplastic Agents/chemistry ; Antineoplastic Agents/pharmacology ; Carbazoles/chemical synthesis ; Carbazoles/chemistry ; Carbazoles/pharmacology ; Cell Line, Tumor ; Cell Proliferation/drug effects ; Dimerization ; Dose-Response Relationship, Drug ; Humans ; Mannich Bases/chemistry ; Oxazines/chemical synthesis ; Oxazines/chemistry ; Oxazines/pharmacology
    Chemical Substances Amines ; Antineoplastic Agents ; Carbazoles ; Mannich Bases ; N,N-bis(carbazolylmethyl)amine ; Oxazines
    Language English
    Publishing date 2010-06
    Publishing country France
    Document type Journal Article
    ZDB-ID 188597-2
    ISSN 1768-3254 ; 0009-4374 ; 0223-5234
    ISSN (online) 1768-3254
    ISSN 0009-4374 ; 0223-5234
    DOI 10.1016/j.ejmech.2010.02.045
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: N-(Hydroxymethyl)ibogaine.

    Jarraya, Raoudha Mezghani / Bouaziz, Amira / Hamdi, Besma / Ben Salah, Abdelhamid / Damak, Mohamed

    Acta crystallographica. Section E, Structure reports online

    2008  Volume 64, Issue Pt 9, Page(s) o1739

    Abstract: The title compound (systematic name: 16-hydroxy-methyl-12-methoxy-ibogamine), C(21)H(28)N(2)O(2 ...

    Abstract The title compound (systematic name: 16-hydroxy-methyl-12-methoxy-ibogamine), C(21)H(28)N(2)O(2), was prepared by reaction of ibogaine with a formaldehyde-acetic acid solution (pH = 4). The crystal structure of this new product, belonging to the iboga indole family, is stabilized by an inter-molecular O-H⋯N hydrogen bond. The identity of the compound was confirmed by one- and two-dimensional NMR spectroscopic techniques.
    Language English
    Publishing date 2008-08-09
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2041947-8
    ISSN 1600-5368
    ISSN 1600-5368
    DOI 10.1107/S1600536808025324
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Effect of two weeks of rTMS on brain activity in healthy subjects during an n-back task: a randomized double blind study.

    Gaudeau-Bosma, Christian / Moulier, Virginie / Allard, Anne-Camille / Sidhoumi, Djedia / Bouaziz, Noomane / Braha, Sonia / Volle, Emmanuelle / Januel, Dominique

    Brain stimulation

    2013  Volume 6, Issue 4, Page(s) 569–575

    Abstract: ... activated during the n-back working memory task.: Objective: The aim of this randomized ... double-blind study was to determine the impact of rTMS applied to the DLPFC on brain activity during an n-back task ... sham coil). Subjects performed an n-back task during two functional magnetic resonance imaging sessions ...

    Abstract Background: Repetitive transcranial magnetic stimulation (rTMS) has shown significant efficiency in the treatment of several psychiatric disorders. In depressive disorders, the dorsolateral prefrontal cortex (DLPFC) is the main target for rTMS, but the effects of this stimulation on cognitive functions and their neural correlates are not well known. Previous works have established that the left DLPFC is reliably activated during the n-back working memory task.
    Objective: The aim of this randomized double-blind study was to determine the impact of rTMS applied to the DLPFC on brain activity during an n-back task in healthy subjects.
    Methods: After randomization, twenty subjects received either active treatment (10 sessions; 1 session a day; frequency = 10 Hz; intensity = 110% of motor threshold) or placebo treatment (sham coil). Subjects performed an n-back task during two functional magnetic resonance imaging sessions (one before stimulation, and one after 10 active or sham rTMS sessions).
    Results: No significant changes, neither in mood nor in performance in the n-back task, were shown. A significant group-by-time interaction effect was found in the bilateral middle frontal gyrus and in the left caudate nucleus.
    Conclusions: These results show that rTMS applied on the left DLPFC had close and remote effects on brain areas involved in working memory.
    MeSH term(s) Adolescent ; Adult ; Aged ; Brain/physiology ; Double-Blind Method ; Female ; Functional Laterality/physiology ; Functional Neuroimaging ; Humans ; Magnetic Resonance Imaging ; Male ; Memory, Short-Term/physiology ; Middle Aged ; Neuropsychological Tests ; Transcranial Magnetic Stimulation/methods
    Language English
    Publishing date 2013-07
    Publishing country United States
    Document type Journal Article ; Randomized Controlled Trial ; Research Support, Non-U.S. Gov't
    ZDB-ID 2394410-9
    ISSN 1876-4754 ; 1935-861X
    ISSN (online) 1876-4754
    ISSN 1935-861X
    DOI 10.1016/j.brs.2012.10.009
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article: N-Methyl-isosalsoline from Hammada scoparia.

    Jarraya, Raoudha Mezghani / Bouaziz, Amira / Hamdi, Besma / Ben Salah, Abdelhamid / Damak, Mohamed

    Acta crystallographica. Section E, Structure reports online

    2008  Volume 64, Issue Pt 9, Page(s) o1714

    Abstract: The title compound (systematic name: 1,2-dimethyl-6-meth-oxy-1,2,3,4-tetra-hydro-isoquinolin-7-ol), C(12)H(17)NO(2), is a major alkaloid isolated from Hammada scoparia leaves. It belongs to the isoquinoline family and it was characterized by NMR ... ...

    Abstract The title compound (systematic name: 1,2-dimethyl-6-meth-oxy-1,2,3,4-tetra-hydro-isoquinolin-7-ol), C(12)H(17)NO(2), is a major alkaloid isolated from Hammada scoparia leaves. It belongs to the isoquinoline family and it was characterized by NMR spectroscopy and X-ray crystallographic techniques. The absolute configuration could not be reliably determined. An intermolecular O-H⋯N hydrogen bond is present in the crystal structure.
    Language English
    Publishing date 2008-08-06
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2041947-8
    ISSN 1600-5368
    ISSN 1600-5368
    DOI 10.1107/S160053680802477X
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: N-(Hydroxymethyl)ibogaine

    Mohamed Damak / Abdelhamid Ben Salah / Besma Hamdi / Amira Bouaziz / Raoudha Mezghani Jarraya

    Acta Crystallographica Section E, Vol 64, Iss 9, Pp o1739-o

    2008  Volume 1739

    Abstract: ... of this new product, belonging to the iboga indole family, is stabilized by an intermolecular O—H.N ...

    Abstract The title compound (systematic name: 16-hydroxymethyl-12-methoxyibogamine), C21H28N2O2, was prepared by reaction of ibogaine with a formaldehyde–acetic acid solution (pH = 4). The crystal structure of this new product, belonging to the iboga indole family, is stabilized by an intermolecular O—H.N hydrogen bond. The identity of the compound was confirmed by one- and two-dimensional NMR spectroscopic techniques.
    Keywords Chemistry ; QD1-999
    Language English
    Publishing date 2008-09-01T00:00:00Z
    Publisher International Union of Crystallography
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  7. Article ; Online: N-Methylisosalsoline from Hammada scoparia

    Mohamed Damak / Abdelhamid Ben Salah / Besma Hamdi / Amira Bouaziz / Raoudha Mezghani Jarraya

    Acta Crystallographica Section E, Vol 64, Iss 9, Pp o1714-o

    2008  Volume 1714

    Abstract: ... configuration could not be reliably determined. An intermolecular O—H.N hydrogen bond is present in the crystal ...

    Abstract The title compound (systematic name: 1,2-dimethyl-6-methoxy-1,2,3,4-tetrahydroisoquinolin-7-ol), C12H17NO2, is a major alkaloid isolated from Hammada scoparia leaves. It belongs to the isoquinoline family and it was characterized by NMR spectroscopy and X-ray crystallographic techniques. The absolute configuration could not be reliably determined. An intermolecular O—H.N hydrogen bond is present in the crystal structure.
    Keywords Chemistry ; QD1-999
    Language English
    Publishing date 2008-09-01T00:00:00Z
    Publisher International Union of Crystallography
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  8. Article: Target specificity of human immunodeficiency virus type 1 NCp7 requires an intact conformation of its CCHC N-terminal zinc finger.

    Ramboarina, S / Druillennec, S / Morellet, N / Bouaziz, S / Roques, B P

    Journal of virology

    2004  Volume 78, Issue 12, Page(s) 6682–6687

    Abstract: The modification of zinc-binding residues inside the conserved CCHC motif of human immunodeficiency virus type 1 NCp7, in particular into CCHH, induces a complete loss of infectivity. Since the mutant His28NCp7 has been shown to be devoid of infectivity ... ...

    Abstract The modification of zinc-binding residues inside the conserved CCHC motif of human immunodeficiency virus type 1 NCp7, in particular into CCHH, induces a complete loss of infectivity. Since the mutant His28NCp7 has been shown to be devoid of infectivity in vivo, the structure-function relationships of the mutant His28(12-53)NCp7 were investigated by nuclear magnetic resonance and surface plasmonic resonance. Although the Cys28-->His mutation modifies drastically the structure of the core domain (residues 12 to 53) of NCp7, His28(12-53)NCp7 still interacts with a 10-fold-lower affinity to specific nucleic acid targets, such as SL3, a stem-loop critically involved in viral RNA packaging, and without affinity change with the nonspecific, single-stranded nucleic acid poly(T). Moreover, His28(12-53)NCp7 and native (12-53)NCp7 displayed the same affinity with reverse transcriptase, but the natures of the complexes are probably different, accounting for the drastic reduction in the amount of RNA packaged in the mutated virus. We propose a structural model of His28(12-53)NCp7 that provides insights into the NCp7 structural features necessary for target recognition and that shows that the specific native structure of the zinc finger domain is strictly required for the optimal target selectivity of NCp7.
    MeSH term(s) Amino Acid Motifs ; Amino Acid Sequence ; Capsid Proteins/chemistry ; Capsid Proteins/genetics ; Capsid Proteins/metabolism ; Gene Products, gag/chemistry ; Gene Products, gag/genetics ; Gene Products, gag/metabolism ; HIV-1/chemistry ; HIV-1/genetics ; HIV-1/metabolism ; HIV-1/pathogenicity ; Humans ; Magnetic Resonance Spectroscopy ; Models, Molecular ; Molecular Sequence Data ; Mutation ; Protein Conformation ; Structure-Activity Relationship ; Surface Plasmon Resonance ; Viral Proteins ; Zinc Fingers/genetics ; gag Gene Products, Human Immunodeficiency Virus
    Chemical Substances Capsid Proteins ; Gene Products, gag ; NCP7 protein, Human immunodeficiency virus 1 ; Viral Proteins ; gag Gene Products, Human Immunodeficiency Virus
    Language English
    Publishing date 2004-06
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 80174-4
    ISSN 1098-5514 ; 0022-538X
    ISSN (online) 1098-5514
    ISSN 0022-538X
    DOI 10.1128/JVI.78.12.6682-6687.2004
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: QSAR Model of Indeno[1,2- b ]indole Derivatives and Identification of N -isopentyl-2-methyl-4,9-dioxo-4,9-Dihydronaphtho[2,3- b ]furan-3-carboxamide as a Potent CK2 Inhibitor

    Samer Haidar / Christelle Marminon / Dagmar Aichele / Abdelhamid Nacereddine / Wael Zeinyeh / Abdeslem Bouzina / Malika Berredjem / Laurent Ettouati / Zouhair Bouaziz / Marc Le Borgne / Joachim Jose

    Molecules, Vol 25, Iss 1, p

    2019  Volume 97

    Abstract: ... derivatives were determined in vitro and one of them ( N -isopentyl-2-methyl-4,9-dioxo-4,9-dihydronaphtho[2,3 ...

    Abstract Casein kinase II (CK2) is an intensively studied enzyme, involved in different diseases, cancer in particular. Different scaffolds were used to develop inhibitors of this enzyme. Here, we report on the synthesis and biological evaluation of twenty phenolic, ketonic, and para -quinonic indeno[1,2- b ]indole derivatives as CK2 inhibitors. The most active compounds were 5-isopropyl-1-methyl-5,6,7,8-tetrahydroindeno[1,2- b ]indole-9,10-dione 4h and 1,3-dibromo-5-isopropyl-5,6,7,8-tetrahydroindeno[1,2- b ]indole-9,10-dione 4w with identical IC 50 values of 0.11 µM. Furthermore, the development of a QSAR model based on the structure of indeno[1,2- b ]indoles was performed. This model was used to predict the activity of 25 compounds with naphtho[2,3- b ]furan-4,9-dione derivatives, which were previously predicted as CK2 inhibitors via a molecular modeling approach. The activities of four naphtho[2,3- b ]furan-4,9-dione derivatives were determined in vitro and one of them ( N -isopentyl-2-methyl-4,9-dioxo-4,9-dihydronaphtho[2,3- b ]furan-3-carboxamide) turned out to inhibit CK2 with an IC 50 value of 2.33 µM. All four candidates were able to reduce the cell viability by more than 60% after 24 h of incubation using 10 µM.
    Keywords qsar ; cancer ; ck2 ; indeno[1,2- b ]indole ; naphtho[2,3- b ]furan-4,9-dione ; Organic chemistry ; QD241-441
    Subject code 540
    Language English
    Publishing date 2019-12-01T00:00:00Z
    Publisher MDPI AG
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  10. Article: Isolated laryngeal tuberculosis: A diagnostic dilemma.

    Bouatay, R / Bouaziz, N / Abdallah, H / Ben Hammouda, S / Koubaa, J

    International journal of surgery case reports

    2024  Volume 116, Page(s) 109376

    Abstract: Introduction and importance: Primary laryngeal tuberculosis (PLTB) is a rare condition. The symptoms and findings are not specific in most of the cases. Patients are diagnosed essentially based on histopathological examination and mycobacterial culture.! ...

    Abstract Introduction and importance: Primary laryngeal tuberculosis (PLTB) is a rare condition. The symptoms and findings are not specific in most of the cases. Patients are diagnosed essentially based on histopathological examination and mycobacterial culture.
    Case report: We report the case of a 42-year-old woman who presented to our hospital with dysphonia and dysphagia. Direct laryngoscopy revealed a lesion of the supraglottis. CT scan found a diffuse thickening of the entire surface of the larynx. A biopsy confirmed the diagnosis of tuberculosis.
    Clinical discussion: Primary laryngeal tuberculosis is a rare clinical entity despite its close anatomical and physiological proximity to the lungs.
    Conclusion: Clinician should keep in mind the existence of primary laryngeal tuberculosis to avoid delayed diagnosis and treatment, which can lead to high morbidity and mortality.
    Language English
    Publishing date 2024-02-10
    Publishing country Netherlands
    Document type Case Reports
    ISSN 2210-2612
    ISSN 2210-2612
    DOI 10.1016/j.ijscr.2024.109376
    Database MEDical Literature Analysis and Retrieval System OnLINE

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