In Vitro Antiproliferative Activity Of Amaryllidaceae Species Against The K562 Human Leukaemia Cell Line

ArticleAcute lymphocytic leukaemia is the most common leukemic cancer reported in children. Chemotherapy is the preferred treatment even though it continues to pose negative side effects of toxicity. Medicinal plants are reported to provide alternative treatment with lower toxicity levels. The three Amaryllidaceae species; Crinum bulbispermum, Boophone disticha, and Amaryllis belladonna Linnaeus have been reported for their anti-leukemic properties. These claims, however, lack supporting scientific data. The study aimed to investigate the anti-proliferative activity of the three Amaryllidaceae species against the human K562 leukaemia cells, as well as their phytochemical composition. The plants’ roots, bulbs and leaves were extracted with water, and sequentially with selected organic solvents. Cell antiproliferation was investigated using the SRB assay. Thin Layer Chromatography was performed to compare chemical profiles of different plant parts, and of plant samples collected fromdifferent geographic areas. Most plant parts tested positive for terpenoids and flavonoids. Only the bulbs contained phytosterols and alkaloids. Plant samples of C. bulbispermum obtained from two geographic areas had similar chemical profiles. Water bulb extract of C. bulbispermum and B. disticha showed over 70% cell growth inhibition at concentration of 10mg/ml, while their methanol extracts showed over 50% cell growth inhibition at 100mg/ml and 10mg/ml.Methanol root extract of A. belladonna L exhibited 100% cell growth inhibition at the concentration of 50mg/ml and over 80% at 25mg/ml concentration. In general, the polar extracts exhibited highest activity. The cell antiproliferation results obtained in this study support the use of the selected Amaryllidaceae species to treat leukemia as currently practiced in traditionalmedicine. The consistency of the constituents of the species, despite of their collection points, could enable standardization of traditionalmedicines

Report containing learning, reflection and evaluation based on social learning:

This report forms the seventh deliverable in the NWRS2 citizen monitoring project and builds on the previous 6 deliverables, which include methodology for the project (Del 1), an assessment of civil society involvement in water policy (Del 2), an overview of the social learning approach and introduction to the case studies (Del 3), draft citizen monitoring guidelines (Del 4), an update on social learning to-date, including action plans (Del 5) and a report on a description and assessment of the case studies (Del 6). This report describes the last social learning module of the ‘Changing Practice’ course and highlights preliminary reflections on the learning that has taken place during this course. The report also describes the plans that were taken at the follow up research meeting. Finally we present the approach towards evaluating the role of social learning in the project as a whole

Citizen Monitoring of The National Water Resource Strategy 2 (NWRS2)

In 2014, the South African Water Caucus (SAWC), a network of non-governmental organisations (NGOs) and community-based organisations (CBOs) who are active in the water sec-tor, embarked on a social learning and action research journey supported by the South African Water Research Commission (WRC) to deepen its monitoring of South Africa’s Second Na-tional Water Resources Strategy (NWRS2). They focused on three issues in three cases study areas

Purification, characterization and three-dimensional structure prediction of multicopper oxidase Laccases from Trichoderma lixii FLU1 and Talaromyces pinophilus FLU12

Abstract Broad-spectrum biocatalysts enzymes, Laccases, have been implicated in the complete degradation of harmful pollutants into less-toxic compounds. In this study, two extracellularly produced Laccases were purified to homogeneity from two different Ascomycetes spp. Trichoderma lixii FLU1 (TlFLU1) and Talaromyces pinophilus FLU12 (TpFLU12). The purified enzymes are monomeric units, with a molecular mass of 44 kDa and 68.7 kDa for TlFLU1 and TpFLU12, respectively, on SDS-PAGE and zymogram. It reveals distinct properties beyond classic protein absorption at 270–280 nm, with TlFLU1's peak at 270 nm aligning with this typical range of type II Cu site (white Laccase), while TpFLU12's unique 600 nm peak signifies a type I Cu 2+ site (blue Laccase), highlighting the diverse spectral fingerprints within the Laccase family. The K m and k cat values revealed that ABTS is the most suitable substrate as compared to 2,6-dimethoxyphenol, caffeic acid and guaiacol for both Laccases. The bioinformatics analysis revealed critical His, Ile, and Arg residues for copper binding at active sites, deviating from the traditional two His and a Cys motif in some Laccases. The predicted biological functions of the Laccases include oxidation–reduction, lignin metabolism, cellular metal ion homeostasis, phenylpropanoid catabolism, aromatic compound metabolism, cellulose metabolism, and biological adhesion. Additionally, investigation of degradation of polycyclic aromatic hydrocarbons (PAHs) by purified Laccases show significant reductions in residual concentrations of fluoranthene and anthracene after a 96-h incubation period. TlFLU1 Laccase achieved 39.0% and 44.9% transformation of fluoranthene and anthracene, respectively, while TpFLU12 Laccase achieved 47.2% and 50.0% transformation, respectively. The enzyme structure–function relationship study provided insights into the catalytic mechanism of these Laccases for possible biotechnological and industrial applications