The prevalence of methicillin-resistant Staphylococcus aureus (MRSA) is slowly rising in Ethiopia for the past few decades. Therefore, novel classes of antibiotics are indispensable to combat the increased incidence of newly emerging multidrug-resistant bacteria like MRSA. Terrestrial flora is considered as a reservoir of novel bioactive secondary metabolites as they have provided us with the largest array of natural products. In this background, the present study is intended to evaluate the in-vitro antibacterial efficacy of five medicinal plants (Ocimum lamiifolium Hochst. ex Benth., Rosmarinus officinalis L, Catharanthus roseus Linn., Azadirachta indica A. Juss and Moringa stenopetala Bac) against a panel of seven biofilm-forming MRSA. The leaves of the plants were extracted in organic solvents of varying polarity and the resultant crude extracts of respective medicinal plants were inspected for their antimicrobial activity by well diffusion technique. Minimum inhibitory concentrations (MIC) and minimum bactericidal concentrations (MBC) of the plant extracts against MRSA were determined by the broth dilution method. Besides, an anti-biofilm assay of the most potent plant extract was also performed, after which its chemical constituents were delineated by combined Gas Chromatographic and Mass Spectroscopic profiling (GC-MS). The results revealed that, of the five plants, three species including M. stenopetala, R. officinalis, and O. lamifolium exhibited significant antibacterial activity. Organic solvents with high and medium polarity were excellent in extracting antimicrobials compared to nonpolar solvents. The broadest and highest rank of activity was observed in the crude ethanolic extract of M. stenopetala. Based on the MIC/MBC ratio, the crude ethanolic extract of M. stenopetala was determined to be bacteriostatic. Anti-biofilm assay showed that the extract of M. stenopetala fairly inhibited the growth of MRSA in the preformed biofilm matrix. The GC-MS analysis of M. stenopetala revealed the presence of twelve compounds with antimicrobial activity. The present study provides new insight into the development of novel drug leads to the management of MRSA.

Background. In developing countries, the prevalence of bacterial infections is quite rampant due to several factors such as the HIV/AIDS pandemic, lack of hygiene, overcrowding, and resistance to conventional antimicrobials. Hence the use of plant-based antimicrobial agents could provide a low-cost alternative therapy. Rosmarinus officinalis is reputed as a medicinal plant in Ethiopia; however, its antibacterial activity against many of the clinical isolates remains overlooked. Methods. Tender foliage of R. officinalis was collected and extracted in ethanol (EtOH) and evaluated for their antimicrobial activity against ten multidrug-resistant (MDR) clinical isolates, human type culture pathogens, and meat-borne bacterial isolates by employing agar well diffusion assay. Results. EtOH extract of R. officinalis efficiently subdued the growth of all tested MDR clinical isolates in varying degrees. Salmonella sp. and Staphylococcus aureus were found to be the most sensitive clinical isolates. Likewise, it efficiently repressed the growth of meat-borne pathogens, particularly, S. aureus and Salmonella sp. showing its potentiality to be used as a natural antibacterial agent in the meat processing industry. The mechanism of antibiosis of plant extract against meat-borne pathogens is inferred to be bactericidal. Chemical constituents of the crude plant extract were analysed by Gas Chromatography-Mass Spectroscopy (GC-MS), Fourier Transform Infrared (FT-IR), and UV-visible spectroscopy showing genkwanin (26%), camphor (13%), endo-borneol (13%), alpha-terpineol (12%), and hydroxyhydrocaffeic acid (13%) as the major compounds. Conclusion. Overall results of the present study conclude that R. officinalis could be an excellent source of antimicrobial agents for the management of drug-resistant bacteria as well as meat-borne pathogens.

Adsorbed on kaolinite, aromatic amines are readily condensed with formaldehyde to give the corresponding diaminodiphenylmethanes. The methodology is novel in its simplicity, selectivity and ecofriendly nature.

Natural Kaolinitic clays containing transition metals Fe and Ti in their lattice have been examined for their acidic properties and catalytic activity for the alkylation of benzene with benzyl chloride. Calcination of the clays at 550 °C and subsequent acid-activation using 2 M HCl (1 M = 1 mol dm−3) rendered the kaolinite surface highly acidic with very high acid amount. These clays exhibited high catalytic activity and selectivity for the conversion of benzyl chloride to diphenylmethane. Al(III), Fe(II), and Ti(II) ions exsolved from the lattice of kaolinites by acid activation relocate in the interlamellar space and boost the Brønsted acidity of coordinated hydroxo and proposed to initiate the alkylation. In fact kaolinites having structural transition metal, on acid activation exhibited higher acid amount and enhanced catalytic activity than kaolinites devoid of transition metals and recently studied alkylation catalysts such as synthetic TiO2–SiO2–Al2O3 and Fe2O3–SiO2–Al2O3. Natural kaolinitic clays having transition metals in their lattice possess disordered structure and hence on acid activation results in the generation of larger amounts of relocatable cations, higher surface area and higher acidity compared to an ideal kaolinite. Also their acid amount and catalytic activity retained up to five successive regeneration cycles studied.

In spite of the great advances in modern medicine in recent decades, medicines of plant origin are still in use for several ailments in different parts of the world. There is always an urge to develop novel, effective and inexpensive antimicrobials. This study was aimed to evaluate the antimicrobial activity and phytochemical composition of the leaf extract of Clematis hirsuta against selected human bacterial and fungal pathogens. Methods: The crude extracts of C. hirsuta leaves were prepared with five different solvents of varying polarity. Agar well diffusion assay on five different species of ATCC organisms, four clinical bacterial isolates, and four clinically isolated fungi were performed. The tube dilution method was used to determine the minimum inhibitory concentrations and the selected extract was subjected to bioassay-guided fractionation using column chromatography and the active fraction obtained were pooled and GC-MS, FT-IR, and CHN analysis were conducted, and this study is actually bioassay-guided research. Results: A varying patterns of antimicrobial activity against tested microorganism was observed. Acetone extract showed the highest spectrum of activity (17-32mm) in the well diffusion assay against bacteria and 16-23mm in the case of fungi. The MIC ranged from 7.5-60 mg/mL in the case of bacteria and 15-60 mg/mL against fungi. The bioassay-guided column chromatography of the acetone extract followed by GC-MS showed the presence of three major compounds, specifically O-ethylhydroxylamine (43%), 2-ethyl heptanoic acid (20.6%), and 1-nonyl cycloheptane (19.5%). The finding was confirmed by FT-IR and elemental analysis of TLCseparated fractions. Conclusion:The acetone extract showed better antimicrobial activity and the least minimum inhibition concentrations against bacteria compared to fungi. The observed antibacterial can be assigned to the presence of alkoxy amine, alkyl aliphatic acids, and cycloalkane. The overall findings substantiate the traditional usages of the parts of this plant, especially the leaves, in managing infectious diseases.