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      Enhanced candicidal compound production by a new soil isolate Penicillium verruculosum MKH7 under submerged fermentation

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          Abstract

          Background

          Microorganisms are a rich source of structurally diverse secondary metabolites that exert a major impact on the control of infectious diseases and other medical conditions. The biosynthesis of these metabolites can be improved by manipulating the nutritional or environmental factors. This work evaluates the effects of fermentation parameters on the production of a lactone compound effective against Candida albicans by Penicillium verruculosum MKH7 under submerged fermentation. Design–Expert version8.0 software was used for construction of the experimental design and statistical analysis of the experimental data.

          Results

          The important factors influencing antibiotic production selected in accordance with the Plackett–Burman design were found to be initial pH, temperature, peptone, MgSO 4.7H 2O. Orthogonal central composite design and response surface methodology were adopted to further investigate the mutual interaction between the variables and identify the optimum values that catalyse maximum metabolite production. The determination coefficient (R 2) of the fitted second order model was 0.9852. The validation experiments using optimized conditions of initial pH 7.4, temperature 27 °C, peptone 9.2 g/l and MgSO 4.7H 2O 0.39 g/l resulted in a significant increase (almost 7 fold from 30 to 205.5 mg/l) in the metabolite production which was in agreement with the prediction (211.24 mg/l). Stability of the compound was also assessed on the basis of its response to physical and chemical stresses.

          Conclusions

          So far as our knowledge goes, till date there are no reports available on the production of antibiotics by Penicillium verruculosum through media optimization using RSM. Optimization not only led to a 7 fold increase in metabolite yield but the same was achieved at much lesser time (8–10 days compared to the earlier 12–15 days). The enhanced yield of the antibiotic strongly suggests that the fungus P. verruculosum MKH7 can be efficiently used for antibiotic production on a large scale.

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          Most cited references49

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          The changing face of candidemia: emergence of non-Candida albicans species and antifungal resistance.

          To assess the changing epidemiology of candidemia in the 1990s, to evaluate the clinical implications for the presence of non-Candida albicans in blood, and to evaluate the presence of antifungal resistance in relation to prior antifungal administration. Multicenter prospective observational study of patients with positive blood cultures for Candida species or Torulopsis glabrata. Four tertiary care medical centers. Four hundred twenty-seven consecutive patients were enrolled. The frequency of candidemia due to non-C. albicans species significantly increased in each hospital throughout the 3.5-year study period (P = 0.01). Thirteen percent of candidemias occurred in patients who were already receiving systemic antifungal agents. Candidemias developing while receiving antifungal therapy were more likely caused by non-C. albicans species than by C. albicans species (P = 0.0005). C. parapsilosis and C. krusei were more commonly seen with prior fluconazole therapy, whereas T. glabrata was more commonly seen with prior amphotericin B therapy. Candida species isolated during episodes of breakthrough candidemia exhibited a significantly higher MIC to the antifungal agent being administered (P < 0.001). In this large scale study, the non-C. albicans species, especially T. glabrata, emerged as important and frequent pathogens causing fungemia. This finding has major clinical implications given the higher complication and mortality rate associated with the non-C. albicans species. The change in the pattern of candidemia might be partly attributed to the increase in number of immunocompromised hosts and the widespread use of prophylactic or empiric antifungal therapy. This is an ominous sign given the in vitro resistance of the non-C. albicans species to currently available antifungal agents.
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            Statistical media optimization and alkaline protease production from Bacillus mojavensis in a bioreactor

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              Use of response surface methodology for optimizing process parameters for the production of α-amylase by Aspergillus oryzae

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                Author and article information

                Contributors
                +9103762372951 , taruncbora@gmail.com
                Journal
                BMC Microbiol
                BMC Microbiol
                BMC Microbiology
                BioMed Central (London )
                1471-2180
                9 December 2016
                9 December 2016
                2016
                : 16
                : 288
                Affiliations
                [1 ]Biotechnology Division, CSIR-North-East Institute of Science & Technology, Jorhat, 785006 Assam India
                [2 ]Department of Life Sciences, Dibrugarh University, Dibrugarh, 786004 Assam India
                Article
                713
                10.1186/s12866-016-0713-8
                5225592
                27938325
                1e1aaa50-e00f-4381-b0a0-a30131f8112c
                © The Author(s). 2016

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 6 October 2015
                : 19 May 2016
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100001412, Council of Scientific and Industrial Research;
                Award ID: 31/25(123)2013-EMR-I
                Award Recipient :
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2016

                Microbiology & Virology
                Microbiology & Virology

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