Microbial development in distillers wet grains produced during fuel ethanol production from corn (Zea mays)

2007 ◽  
Vol 53 (9) ◽  
pp. 1046-1052 ◽  
Author(s):  
R. Michael Lehman ◽  
Kurt A. Rosentrater

Distillers grains are coproduced with ethanol and carbon dioxide during the production of fuel ethanol from the dry milling and fermentation of corn grain, yet there is little basic microbiological information on these materials. We undertook a replicated field study of the microbiology of distillers wet grains (DWG) over a 9 day period following their production at an industrial fuel ethanol plant. Freshly produced DWG had a pH of about 4.4, a moisture content of about 53.5% (wet mass basis), and 4 × 105 total yeast cells/g dry mass, of which about 0.1% were viable. Total bacterial cells were initially below detection limits (ca. 106 cells/g dry mass) and then were estimated to be ∼5 × 107 cells/g dry mass during the first 4 days following production. Culturable aerobic heterotrophic organisms (fungi plus bacteria) ranged between 104 and 105 CFU/g dry mass during the initial 4 day period, and lactic acid bacteria increased from 36 to 103 CFU/g dry mass over this same period. At 9 days, total viable bacteria and yeasts and (or) molds topped 108 CFU/g dry mass and lactic acid bacteria approached 106 CFU/g dry mass. Community phospholipid fatty acid analysis indicated a stable microbial community over the first 4 days of storage. Thirteen morphologically distinct isolates were recovered, of which 10 were yeasts and molds from 6 different genera, 2 were strains of the lactic-acid-producing Pediococcus pentosaceus and only one was an aerobic heterotrophic bacteria, Micrococcus luteus . The microbiology of DWG is fundamental to the assessment of spoilage, deleterious effects (e.g., toxins), or beneficial effects (e.g., probiotics) in its use as feed or in alternative applications.

2014 ◽  
Vol 1040 ◽  
pp. 319-322
Author(s):  
E.V. Bulycheva ◽  
E.I. Korotkova ◽  
O.A. Voronova

In this paper for investigation of the medicine «Lactobacterin» containing lactic acid bacteria was used luminescence method. It is shown, that spectrum of the Lactobacilli has 3 peaks from different substances. It is shown that during 2 hours the bacterial cells are alive.


Author(s):  
Anik Ma'unatin ◽  
Harijono Harijono ◽  
Elok Zubaidah ◽  
Muhaimin Rifa'i

Background and Objectives: Lontar (Borassus flabellifer L.) is widely grown in Indonesia and one of its products is palm sap. Palm sap contains a high level of sugar, making it suitable as a medium to increase the lactic acid bacteria (LAB) production of exopolysaccharides (EPS). This study aimed to isolate the EPS-producing LAB from palm sap and evaluate its EPS production. LAB isolation was carried out on MRS agar containing 0.5% CaCO3 . Materials and Methods: The screening and production of EPS were carried out on MRS media supplemented with 10% sucrose. The molecular identification of the selected EPS-producing LAB was based on 16S rDNA. A quantitative analysis of EPS polymer dry mass and total sugar was conducted using one-way ANOVA. Results: In this study, five EPS-producing LABs were found: Fructobacillus fructosus N4, Leuconostoc mesenteroides N5, Leuconostoc mesenteroides N7, Leuconostoc mesenteroides N9, and Fructobacillus fructosus N10. The highest EPS yield in liquid media was 10.997 ± 1.591 g/L by Leuconostoc mesenteroides N7, whereas the lowest was 4.505 ± 0.459 g/L by Fructobacillus fructosus N10. Conclusion: This study found Fructobacillus fructosus strains as EPS producers that have never been reported before.


2019 ◽  
Vol 8 (4) ◽  
pp. 12858-12860

In the field of microbiology, digital image analysis methods are receiving significant attention to automatically interpret images of bacterial cells. An automatic procedure to extract and classify images of lactic acid bacteria (LAB) is presented in this paper. Edge based watershed method with automatically generated markers were used to retain the image information at fine scales. The experiment was conducted on images containing one type of bacteria. The scanning electron microscopic (SEM) images of lactic acid bacteria (LAB) are used in this experiment. The image analysis and classification technique described in this paper is quick and simple to recognize organisms based on their morphological characteristics. The classification results indicate that routine methods for the detection, enumeration and identification of bacteria can be automated with use of direct microscopic methods


2017 ◽  
Vol 2 (2) ◽  
pp. 79
Author(s):  
Suryani Suryani ◽  
Dedi Nofiandi ◽  
Husni Mukhtar ◽  
Melona Siska ◽  
Abdi Dharma ◽  
...  

<p><em>Virgin Coconut Oil is an oil of coconut milk fermentation that has many uses such as can prevent HIV, because it functions as antibacterial, antifungal and antiviral. Antibacterial, antifungal and antiviral agents are found in bacteria lactic acid bacteriocin, a peptide that can destroy bacterial cells and pathogenic fungi and viral cells. The aim of this study was to identify molecularly lactic acid bacteria isolated and morphologically identified and biochemical tests, from fermented coconut milk. Apparently lactic acid bacteria is Lactobacillus paracasei strain 1.7.</em></p><p> </p><p>Virgin Coconut Oil adalah minyak dari fermentasi santan kelapa yang mempunyai banyak sekali kegunaan diantaranya  dapat mencegah HIV, karena berfungsi sebagai antibakteri, antijamur dan antivirus. Zat antibakteri, antijamur dan antivirus itu terdapat pada bakteri asam laktat yaitu bakteriosin, berupa peptida yang dapat menghancurkan sel bakteri dan jamur patogen serta sel virus. Tujuan penelitian ini adalah mengidentifikasi secara molekular bakteri asam laktat  yang telah diisolasi dan diidentifikasi secara morfologi dan uji – uji biokimia, dari santan yang difermentasi.  Ternyata bakteri asam laktat nya adalah Laktobacillus paracasei strain 1.7.</p><p> </p>


The Analyst ◽  
2015 ◽  
Vol 140 (17) ◽  
pp. 5920-5928 ◽  
Author(s):  
Stéphanie Passot ◽  
Julie Gautier ◽  
Frédéric Jamme ◽  
Stéphanie Cenard ◽  
Paul Dumas ◽  
...  

Combining synchrotron-FTIR microspectroscopy and fluorescence microscopy made it possible the simultaneous assessment of biochemistry and physiological state of small bacterial cells for better understanding the mechanisms of cell cryotolerance.


2007 ◽  
Vol 73 (14) ◽  
pp. 4673-4676 ◽  
Author(s):  
Taketo Kawarai ◽  
Soichi Furukawa ◽  
Hirokazu Ogihara ◽  
Makari Yamasaki

ABSTRACT We found that species combinations such as Lactobacillus casei subsp. rhamnosus IFO3831 and Saccharomyces cerevisiae Kyokai-10 can form a mixed-species biofilm in coculture. Moreover, the Kyokai-10 yeast strain can form a biofilm in monoculture in the presence of conditioned medium (CM) from L. casei IFO3831. The active substance(s) in bacterial CM is heat sensitive and has a molecular mass of between 3 and 5 kDa. In biofilms from cocultures or CM monocultures, yeast cells had a distinct morphology, with many hill-like protrusions on the cell surface.


2018 ◽  
Vol 22 (1) ◽  
pp. 1
Author(s):  
Rohmatussolihat Rohmatussolihat ◽  
Puspita Lisdiyanti ◽  
Yopi Yopi ◽  
Yantyati Widyastuti ◽  
Endang Sukara

Lactic acid bacteria (LAB) are important for prevention of spoilage and pathogenic bacterial growth in foods due to their ability to generate antimicrobial substances. The objective of this study was to screen LAB for antimicrobial activity and to optimize culture medium for antimicrobial production using Response Surface Methodology (RSM) with Central Composite Design (CCD). Optimization of antimicrobial production of selected LAB was conducted with different combinations of glucose, NaCl, inoculum, and temperature. Our experimental results showed that from 129 LAB isolates, 55 showed significant inhibition against Bacillus subtilis, Escherichia coli, Micrococcus luteus, Staphylococcus aureus, Aspergillus niger, and Candida albicans. No isolates inhibited the growth of Aspergillus flavus. Lactobacillus plantarum LIPI13-2-LAB011 was selected for further study on culture medium optimization to inhibit the growth of C. albicans. From statistical analysis, the production of antimicrobial substances was significantly influenced by temperature, NaCl, and concentration of glucose. Furthermore, the optimum concentrations of glucose, concentration of inoculum, temperature, and NaCl were 1.63 %, 3.03%, 33.74°C, and 3.4%, respectively, with a maximum predicted inhibition index of 1.916, which increased 3.56-fold compared to that obtained in medium before optimization processes. The result was confirmed as when the optimum concentration of nutritions used, the inhibition index increased 3.12-fold.


2021 ◽  
Author(s):  
Ryan M Kalinoski ◽  
Wenqi Li ◽  
Justin K Mobley ◽  
Xiaowen Chen ◽  
Sue E Nokes ◽  
...  

Lactic acid bacteria (LAB) contamination during fuel ethanol fermentation can lead to significant economic loses. To circumvent this, fuel ethanol plants add antibiotics prophylactically, but their overuse has resulted in...


2015 ◽  
Vol 5 (3) ◽  
pp. 101-106
Author(s):  
Dinesh Kumar Kumawat ◽  
Nadim Chishty

  Lactic acid bacteria (LAB) are a group of gram positive, non spore forming, cocci or rod shaped, catalase negative organisms. Generally they are known as "GRAS" (Generally Recognized As Safe) organisms. In the present study, an attempt was made to isolate lactic acid bacteria from gut of two freshwa-ter fishes in Udaipur region to obtain various efficient LAB strains for indus-trial applications. A total of 12 bacterial isolates were isolated from different fishes caught from Pichola lake, Udaipur on MRS agar at 37oC. All the isolates were tested for catalase activity, colony morphology and gram staining. Further these isolates were checked for technological properties (antibacterial activity, antibiotic susceptibility and bile salt tolerance). Based on technologi-cal properties results, two isolate (F-4 & F-11) have been tentatively selected for use as probiotic cultures in the aquaculture industries. They have strong antibacterial activity against various pathogens viz. Staphylococcus aureus (ATCC 9144), Micrococcus luteus (ATCC 10240), Listeria monocytogens (MTCC 1143) and have bile salt tolerance limit up to 0.7%. These are the main features for selection of probiotic candidates. To differentiate the same species molecular typing was attempted, 16S rRNA gene amplification was done using specific 16S rDNA primers and amplified gene products were di-gested with different restriction endonuclease enzymes viz EcoRI and HindIII. A total of 2 different groups out of 12 isolates were obtained. This finding reveals that isolated LAB are useful for aquaculture and also used in food preservation.


2020 ◽  
Vol 10 (5) ◽  
pp. 170-176
Author(s):  
A.P. Paliy ◽  
S.O. Gujvinska ◽  
M.V. Kalashnyk

The aim of this work was to develop a technological regulation for the production of probiotic based on lacto- and bifidobacteria in the form of intestinal-soluble capsules for farm animals. Three experimental series of probiotic drug were made in the form of enteric capsules based on lactic acid bacteria. It has been established that the Bifidobacterium adolectentis No 17-316 strain and the Lactobacillus plantarum No 7-317 strain are the most adapted for the bacterial consortium. These strains have high biological activity and correspond to certain authentic characteristics. The pharmaceutical composition is proposed in the form of capsules with following ingredients: 50% of dry biomass of Lactobacillus plantarum No 7-317 and Bifidobacterium adolectentis No 17-316 strains, 5% of glucose, 5% of lactose, 9% of aerosil and 31% of starch. The content of lyophilized bacteria in one capsule is not less than 1 × 107 CFU of bifidobacteria/cm3 and 1 × 107 CFU of lactobacilli/cm3. A scheme of the manufacturing process of the drug in form of capsules includes the following stages: production of nutrient media and working solutions; growing cultures of lacto- and bifidobacteria, freeze drying of cultures of lacto- and bifidobacteria, obtaining a dry mass of lactic acid bacteria for encapsulation, encapsulation of the drug, control of the manufactured product before release, marking, packaging of capsules, transportation, storage of a drug.


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