Potato tuber skin (suberin), isolated enzymatically, was depolymerized with BF3‐CH3OH, and the structure and composition of the aliphatic monomers were determined by combined gas chromatography‐mass spectrometry. 18‐Hydroxyoctadec‐9‐enoic acid and octadec‐9‐ene‐1,18‐dioic acid were the major components. Products of epoxidation and subsequent hydration of the Δ9 double bond of these compounds, 10,16‐dihydroxy hexadecanoic acid, and much smaller quantities of 9,16‐dihydroxyhexadecanoic acid and 8,16‐dihydroxyhexadecanoic acid also were present. The other significant feature of the monomer composition of potato skin was that it contained substantial quantities of C20−C28 fatty acids, fatty alcohols, and ω‐hydroxy acids. Based upon these studies, a method of distinguishing between suberin and cutin and a biosynthetic pathway for suberin monomers are suggested.

Seventy-nine Actinomycetes were isolated from soils of Kalapatthar (5545m), Mount Everest region. Twenty seven (34.18%) of the isolates showed an antibacterial activity against at least one test-bacteria among two Gram positive and nine Gram negative bacteria in primary screening by perpendicular streak method. Thirteen (48.15%) showed antibacterial activity in secondary screening. The result showed that three of the isolates, K.6.3, K.14.2, and K.58.5 were highly active with an inhibition zone e"20mm and broad spectrum antibacterial activity including two methicillin resistant Staphylococcus aureus (MRSA) strains. Minimum inhibitory concentration (MIC) of antibacterial metabolites of the isolate K.6.3 was 1mg/ml, and that of isolates K.14.2 and K.58.5 was 2mg/ml. Two spots were detected on thin layer chromatography plate from each of the metabolites which was completely different from the spot produced by vancomycin. The active isolates from primary screening were heterogeneous in their overall macroscopic, biochemical, and physiological characteristics through unweighted pair group method using average (UPGMA) cluster analysis. Delineation of the three active isolates showing potent broad spectrum antibacterial activity revealed that they belonged to distinct taxonomic groups.

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BackgroundCholera, an infectious disease caused by Vibrio cholerae, is a major public health problem and is a particularly burden in developing countries including Nepal. Although the recent worldwide outbreaks of cholera have been due to V. cholerae El Tor, the classical biotypes are still predominant in Nepal. Serogroup O1 of the V. cholerae classical biotype was the primary cause of a cholera outbreak in Kathmandu in 2012. Thus, this study was designed to know serotypes and biotypes of V. cholerae strains causing recent outbreak with reference to drug resistant patterns. Moreover, we also report the toxigenic strains of V. cholerae from both environmental and clinical specimens by detecting the ctx gene.MethodsTwenty four V. cholerae (n = 22 from stool samples and n = 2 from water samples) isolated in this study were subjected to Serotyping and biotyping following the standard protocols as described previously. All of the isolates were tested for antimicrobial susceptibility patterns using the modified Kirby-Bauer disk diffusion method as recommended by CLSI guidelines. The screening of the ctx genes (ctxA2-B gene) were performed by PCR method using a pair of primers; C2F (5′-AGGTGTAAAATTCCTTGACGA-3′) and C2R (5′-TCCTCAGGGTATCCTTCATC-3′) to identify the toxigenic strains of V. cholerae.ResultsAmong twenty four V. cholerae isolates, 91.7% were clinical and 8.3% were from water samples. Higher rate of V. cholerae infection was found among adults of aged group 20–30 years. All isolates were serogroups O1 of the V. cholerae classical biotype and sub serotype, Ogawa. All isolates were resistant to ampicillin, nalidixic acid and cotrimoxazole. 90.9% were resistant to erythromycin however, tetracycline was found to be the most effective drug for the isolates. All isolates were multidrug resistant (MDR) and possessed a ctx gene of approximately 400 base pairs indicating the toxigenic strains.ConclusionHundred percent strains of V. cholerae were MDR possessing a ctx gene. It suggests that toxigenic strains be identified and proper antibiotic susceptibility testing be conducted. This will allow effective empirical therapy to be used to treat and control cholera.