Identification and Distribution of Bacillus Species in Doenjang by Whole-Cell Protein Patterns and 16S rRNA Gene Sequence Analysis
Institute of Life Sciences & Resources and Graduate School of Biotechnology, Kyung Hee University, Yongin, Korea. Journal of Microbiology and Biotechnology
(Impact Factor: 1.53).
08/2010; 20(8):1210-4. DOI: 10.4014/jmb.1002.02008
Many bacteria are involved in fermentation of doenjang and Bacillus species are known to perform significant roles. Although the SDS-PAGE technique has been frequently used for classification and identification of bacteria in various samples, there has been no investigation of the microbial diversity in doenjang. This study aims to investigate the identification and distribution of dominant Bacillus species in doenjang using SDS-PAGE profiles of whole cell proteins and 16S rDNA sequencing. SDS-PAGE of whole cell proteins of the reference Bacillus strains yielded differential banding patterns that could be considered to be highly specific fingerprints. Bacterial strains isolated from doenjang samples were grouped using whole cell protein patterns, which were confirmed by the analysis of 16S rDNA sequencing. B. subtilis was found to be the most dominant strain in most of the samples, and B. licheniformis and B. amyloliquefaciens were less frequently detected. The results obtained in this study showed that a combined identification method, SDS-PAGE patterns of whole cell proteins and subsequent 16S rDNA sequence analysis, could successfully identify Bacillus species isolated from doenjang.
Available from: Maria Anita Mendes
- "These methods are time-consuming and do not provide an insight into the physiological properties of the microorganism.    Koichi Tanaka, the winner of the Nobel Prize in Chemistry in 2002, developed a method using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry "
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ABSTRACT: RATIONALEDue to increases in greenhouse gas emissions, it is necessary to explore renewable sources of energy. Interesting alternatives are biofuels derived from microalgae. One challenge is the development of a detailed microalgae database compiling species identifications and characterizations that would facilitate microalgae selection for biomass production. Mass spectrometric (MS) analysis using a matrix-assisted laser desorption/ionization (MALDI) source is an advanced technique that enables advancement in this biological area. In this work a MALDI time-of-flight (TOF)MS method for the rapid identification of proteins in whole cells of selected microalgae species was studied. Furthermore, the efficiency of different matrix and solvent systems was tested. MS analyses were performed using an UltrafleXtreme MALDI-TOF mass spectrometer operating in linear positive ion mode. METHODS
Mass spectra were acquired in a mass range from 4000 to 20,000 Da with ions generated from Smartbeam laser irradiation using a frequency of 2000 Hz, a PIE 100 ns and a lens 7 kV. The voltage was 25 kV for the first ion source and 23 kV for the second. Each spectrum was generated by averaging of 10,000 laser shots and the laser irradiance was set at 95-100%. RESULTSSimilar mass spectra were obtained for all matrices (SA, HCCA, DHB and sDHB); however, the use of the sDHB matrix resulted in spectrum profiles with a greater amount number of proteins, a better signal/noise (S/N) ratio and higher intensities for the majority of microalgae analyzed. Trifluoroacetic acid (TFA) content was also studied and the best results in terms of S/N ratio, number of proteins and signal intensities were obtained with 0.1% TFA in the matrix solvent. The addition of isopropanol did not produce improvement in the quality of spectrum profiles. CONCLUSIONS
Therefore, the optimal matrix for the analysis of protein from intact microalgae cells is sDHB with TA50 as the matrix solvent and without isopropanol. These conditions allow the acquisition of high quality spectrum profiles. Copyright (c) 2014 John Wiley & Sons, Ltd.
Available from: Jing Wang
- "The presence of cfr was screened by PCR with previously described primers
. Species identification of the cfr-carrying strains was performed by the API-Staph System (bioMérieux, France) and further confirmed by 16S rRNA sequencing
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The emergence and wide distribution of the transferable gene for linezolid resistance, cfr, in staphylococci of human and animal origins is of great concern as it poses a serious threat to the public health. In the present study, we investigated the emergence and presence of the multiresistance gene, cfr, in retail meat sourced from supermarkets and free markets of Guangzhou, China.
A total of 118 pork and chicken samples, collected from Guangzhou markets, were screened by PCR for cfr. Twenty-two Staphylococcus isolates obtained from 12 pork and 10 chicken samples harbored cfr. The 22 cfr-positive staphylococci isolates, including Staphylococcus equorum (n = 8), Staphylococcus simulans (n = 7), Staphylococcus cohnii (n = 4), and Staphylococcus sciuri (n = 3), exhibited 17 major SmaI pulsed-field gel electrophoresis (PFGE) patterns. In 14 isolates, cfr was located on the plasmids. Sequence analysis revealed that the genetic structures (including ΔtnpA of Tn558, IS21-558, ΔtnpB, and tnpC of Tn558, orf138, fexA) of cfr in plasmid pHNTLD18 of a S. sciuri strain and in the plasmid pHNLKJC2 (including rep, Δpre/mob, cfr, pre/mob and partial ermC) of a S. equorum strain were identical or similar to the corresponding regions of some plasmids in staphylococcal species of animal and human origins.
To the best of our knowledge, this is the first study to report the presence of the multiresistance gene, cfr, in animal meat. A high occurrence of cfr was observed in the tested retail meat samples. Thus, it is important to monitor the presence of cfr in animal foods in China.
Available from: Reham Elbaz
- "Cellular protein samples were prepared according to Kim et al. (2010). Flasks (250 ml) each containing 50 ml LB broth were inoculated with the bacterial species and incubated overnight at 20, 25, 30, 35, 40, 45 and 50 @BULLETC by shaking until OD 600 ~0.4, "
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ABSTRACT: Three gram positive bacterial isolates, isolated from soil and identified as Bacillus licheniformis, Bacillus circulans and Geobacillus thermoglucosidasius were grown at 20, 35, and 50 o C then subjected to cellular fatty acids analysis. Although in different amounts, the fatty acids (10:0), (12:0), (14:0), (16:0) and (17:0) were detected in cells of the three bacterial isolates obtained from all the incubation temperatures. Increasing temperature from 20 to 50 o C raised the proportion of the saturated fatty acids by 26.10%, 09.89% and 29.61% in B. licheniformis, B. circulans and G. thermoglucosidasius, respectively. Cellular protein contents and protein banding pattern on SDS-PAGE of the three isolates were estimated at 20, 25, 30, 35, 40, 45 and 50 o C. The highest amount of protein concentration in all isolates was obtained at 20ºC. In contrast, the highest number of protein bands was not obtained from these treatments.
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