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Caractérisation biomoléculaire et biotechnologique des souches de « Saccharomyces cerevisiae » issues des cépages Algériens
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| dc.contributor.author | BERBER, Nadia | |
| dc.date.accessioned | 2017-11-08T15:09:09Z | |
| dc.date.available | 2017-11-08T15:09:09Z | |
| dc.date.issued | 2017-10-31 | |
| dc.identifier.uri | http://hdl.handle.net/123456789/550 | |
| dc.description.abstract | RESUME Le raisin est un fruit exemplaire de la diversité microbienne, il est considéré comme l’habitat de multiples micro-organismes parmi les quels les levures. Dans ce cadre, cette étude consiste à isoler des souches indigènes de la levure « Saccharomyces cerevisiae » à partir de moût raisin (1er jour de fermentation) issus des différents cépages algériens (Muscat noir, Cinsault et Carignan), et à les identifier d’abord sur le plan microscopique puis moléculaire où on s’intéresse d’une part à l’étude de la région Delta par PCR-Delta, et d’autre part la variabilité de l’ADNr , plus exactement la région ITS1-5,8S-ITS2 par PCR-ITS-RFLP. Sur les 34 isolats de levures isolés, 06 genres et 12 espèces différentes ont été caractérisées selon leur profil moléculaire et différenciées par l’emploi de deux enzymes de restriction (HinfI et HaeIII). Parmi ces espèces, 03 souches de Saccharomyces cerevisiaeMn11 (9ème j) (AT), Cn11 (9ème j) (MOS) et Cr3 (9ème J) (MOS) ont été identifiées, ayant des formes végétatives ovoïdes, se propagent par bourgeonnement monopolaire, caractérisées par un puissant pouvoir fermentaire (forte production de CO2 et d’éthanol) et possédant l’enzyme « invertase ». Les 31 souches restantes sont des espèces non Saccharomyces, identifiées comme appartenant à différents genres tels que Torulaspora, Candida, Pichia, Hanseniaspora et Zygosaccharomyces. Elles se multiplient par différents modes de reproduction (monopolaire, bipolaire et multipolaire) et sont caractérisées par des formes végétatives cylindriques, parfois sphériques, allongées ou courtes. Cependant, les levures non Saccharomyces sont très présentes, même majoritaires, dans les moûts de raisin du Muscat noir, du Cinsault et de Carignan par rapport aux levures Saccharomyces. Mots clés: Raisin, Levures, Saccharomyces cerevisiae, PCR-Delta, PCR-ITS-RFLP, Invertase. SUMMARY The grape is an exemplary fruit of the microbial diversity, it is considered as the habitat of multiple microorganisms among which the yeasts. In this framework, this study consists of isolating native strains of the "Saccharomyces cerevisiae" yeast from grape must (first day of fermentation) from different Algerian grape varieties (Muscat noir, Cinsault and Carignan), and to identify them first on the microscopic and then on the molecular level, where we are interested on the one hand in the study of the Delta region by PCR-Delta, and on the other hand the variability of the rDNA, region ITS1-5,8S-ITS2 by PCR-RFLP-ITS. Of the 34 isolated yeast isolates, 06 genera and 12 different species were characterized according to their molecular profile and differentiated by the use of two restriction enzymes (HinfI and HaeIII). Among these species, 03 strains of Saccharomyces cerevisiae Mn11 (9th J) (AT), Cn11 (9th J) (MOS) and Cr3 (9th J) (MOS) were identified, with ovoid vegetative forms, propagated by monopolar budding, Characterized by a strong fermentative power (high production of CO2 and ethanol) and possessing the enzyme « invertase». The remaining 31 strains are non-Saccharomyces species, identified as belonging to different genera such as Torulaspora, Candida, Pichia, Hanseniaspora and Zygosaccharomyces. They multiply by different modes of reproduction (monopolar, bipolar and multipolar) and are characterized by cylindrical vegetative forms, sometimes spherical, elongated or short. However, non-Saccharomyces yeasts are very present, even in the majority, in the grape musts of Muscat noir, Cinsault and Carignan compared to Saccharomyces yeasts. Key words: Grape, Yeasts, Saccharomyces cerevisiae, PCR-Delta, PCR-RFLP-ITS, Invertase. | en_US |
| dc.language.iso | fr | en_US |
| dc.publisher | Advances inEnvironmental Biology, 10(12) December 2016, Pages: 55-61 AENSI Journals Advances inEnvironmental Biology ISSN-1995-0756 EISSN-1998-1066 Journal home page: http://www.aensiweb.com/AEB/ Copyright © 2016 by authors and Copyright,American-Eurasian Network for Scientific Information (AENSI Publication). Isolation and Molecular Identification (PCR-Delta and PCR-RFLP-ITS) of the yeast from Black muscat grape cultived in El malah (Wilaya of Ain Temouchent, Algeria) 1Nadia BERBER,2Rachid AISSAOUI, 1Ahmed Mohamed Ali BEKADA, 3Morvan COARER 1Technology of Food and Nutrition Laboratory (University of Abdelhamid Ibn Badis, Mostaganem), 27000, ALGERIA. 2Bioconversion Laboratory (University of Mustapha STAMBOULI, Mascara), 29000, ALGERIA. 3Microbiology and Biotechnology Laboratory (French Institute of Vine and Wine of Nantes), 44000, France. Address For Correspondence: Nadia BERBER, Technology of Food and Nutrition Laboratory (University of Abdelhamid Ibn Badis, Mostaganem), 27000, ALGERIA. E-mail: nadia.berber27@gmail.com This work is licensed under the Creative Commons Attribution International License (CC BY).http://creativecommons.org/licenses/by/4.0/ Received 16 November 2016; Accepted 17 December 2016; Available online 22 December 2016 ABSTRACT The grape is an exemplary product of microbial diversity, it is considered as home to many wild microorganisms (yeast). In this context, we explored in this study, the divergence of the indigenous yeast flora in the vineyards of the region El Malah (Wilaya of Ain Temouchent, Algeria) by collecting varietal grape samples (Black Muscat). A high molecular diversity of the flora has been demonstrated, using two molecular techniques, where one is interested in the study of variability of rDNA, more precisely the region 5,8S rRNA ITS1-ITS2 by PCR-RFLP-ITS and the region Delta by PCR-Delta is an additional study which helped sort the yeast Saccharomyces and non Saccharomyces.So 6 yeast species belonging to the 11 studied at 4 different types were characterized according to their molecular profiles. Thus the strains studied were characterized by two restriction enzymes (HinfI and HaeIII). Meanwhile, microscopic and macroscopic studies of classical identification of yeast were able to strengthen these results. Among the yeast species identified: Torulaspora delbrueckii, Torulaspora pretoriensis, Candida solani, Candida pseudointermedia and Saccharomyces cerevisiae. This variety is an excellent tank of non Saccharomyces yeasts as evidenced by the results.However, the tools of molecular biology have brought a notorious revolution in precise yeast identification tests. The PCR-RFLP-ITS is one of the most widely used methods of identification. KEYWORDS:Grape, Yeast, Black Muscat, PCR-Delta, PC-RFLP-ITS, HinfI, HaeIII. INTRODUCTION Yeasts are naturally present on soils, plant surfaces, especially grape berries, or in wine-growing areas [3,23]. Their dissemination is assured by wind, insects and humans through its various interventions on the environment [1,13].The yeast species present on the surface of the grape berries are significantly limited in number. The density of the yeasts evolves during the maturation of the grapes. The evolution of yeast populations may be related to the increase in the area of the bay and the availability of nutrients: during the maturation of the bunch, the berries grow, the nutrient content Surface area increases, sugar concentration increases and acidity decreases [4,9].The representation of the different yeasts varies during the development of the grape berry according to several parameters: grape variety, climatic conditions, soil, wine practices, age of vines, health status of the cluster and the degree of maturity of the grape [8,10,33]. Black Muscat is a black table grape varietal. It is characterized by beautiful black cohosh, juicy flesh, staining grain is sometimes clear. This variety is fairly resistant to drought and likes in sunny areas. The grape 56 Nadia BERBER et al, 2016 Advances in Environmental Biology, 10(12) December 2016, Pages: 55-61 whether table or tank is the habitat of many wild microorganisms since it is considered the kingdom of yeasts. However, the high sugar content of the Muscat grape must (300 g / l) promotes the growth of yeast, these microorganisms play an essential role in the food industry. They participate in the development of many food products (bread, dairy, brewery) and the production of metabolites (lipids, proteins, enzymes), but also the upgrading of agricultural and industrial waste. However, many yeast species produce a very important primary metabolite namely ethanol, used as fuel or for other industrial purposes [17]. Two strains of bacteria were isolated from the gut of termite in different media. It was observed that these isolates have produced ethanol from rice straw (7.52 ± 0.5 to 9.33 ± 0.4 g/L) followed by corn stove (6.35 ±0.6 to 6.95 ±0.5 g/L) having theoretical yields of ethanol 43.31 % (rice straw) and 39.62 % ( corn stove) [16]. The aim of this study is to isolate, characterize microscopically and identify the indigenous species of yeasts found in the grape variety (Black Muscat) grown in the region of El Maleh (Ain Temouchent, Algeria) to develop and express the diversity of the phylogenetic heritage based on the two molecular techniques (PCR-Delta and PCR-RFLP-ITS). Our work is an initiative for the creation of a "Souchier" typical yeast our country Algeria. MATERIAL AND METHODS Grape picking Source (Black Muscat): The samples are taken randomly in the month of September 2014 in the vineyards of the city El Malah, a town located 11 Km from Ain Temouchent. We collected with sterile scissors, about 500 g healthy grapes, and it was collected in sterile bags. A laboratory arrival, they are scuffed and crushed to obtain a mash and ferment for one day at 25 ° C in order to increase the viability and quantityof the desired yeast [30]. Isolation, purification and conservation of cultures: We conducted a series of seeding by the method streaks on plates of agar cultures (YPG + Gentamicin) which aims to have pure cultures. The operation is repeated in each time taking random an isolated colony. Next, the purified strains are placed in a glycerol solution (sterile) with approximately 25% and stored in the freezer at -18 ° C. Microbiological identification: Study of characters crop: After incubating the cultures for 3 days at 25-28 ° C on agar medium (YPG + Gentamicin), macroscopic observation can describe the appearance of colonies (size, pigmentation, contour, viscosity ...) [17]. The cellular characteristics: Microscopic observation to define the shape, arrangement and mode of cell division. These characteristics are observed on microscopic slides to fresh (40 x objective) [25]. Molecular identification: DNA extraction: The isolation of DNA from biological samples is a crucial step in the process of DNA-based molecular biological assays [27]. Before extracting genomic DNA from strains levuriennes, these have been cultured in the medium (liquid YPG + Gentamicin), then a small amount of culture was taken and centrifuged to separate the cells. After the supernatant was removed and the lysis of the resulting pellet of cells was performed by addition of a volume of 660 μl of SDS-50TE mix (lysis buffer).Then the mixture was incubated at 65°C for 10 minutes. To neutralize the medium, a volume of 340 μl of potassium acetate was added to the mixture, the latter is placed in the refrigerator for 30 minutes until the suspension became semi-solid. Then a second centrifugation was performed for 10 minutes and a volume of 750 μl of supernatant was mixed with 750 μl of isopropanol followed by a final centrifugation to precipitate DNA. Then, the collected DNA pellet was rinsed gently with approximately 100 μl of 95% ethanol, then suspended in a volume of 300 μl of TE1x (storage buffer) and incubated at 65 ° C for 15 minutes. Finally, the DNA was stored refrigerated 4°C until use. (According to IFV Nantes, 2012). Amplifying the target region by the two molecular techniques (PCR-Delta and PCR-RFLP-ITS): PCR-Delta (Delta 12 / Delta 21): Typing of strains of Saccharomyces cerevisiae is performed by PCR using the method developed by [18] with the primers: δ 12 (5'-TCAACAATGGAATCCCAAC-3 ') δ 21 (5'-CATCATTAACACCGTATATGA-3 ').The reaction mixture is summarized in Table 1. 57 Nadia BERBER et al, 2016 Advances in Environmental Biology, 10(12) December 2016, Pages: 55-61 Table 1: The composition of the reaction mixture used for PCR-Delta according to (IFV) Products Volume (μl ) Volumes (μl) H2O 1220 1230 Tampon 10X 160 160 dNTP 64 64 Delta 1 or 12 8(40pmol ̸ reaction) 8 Delta 2 or 21 8(40pmol ̸ reaction) 8 Mgcl2 80 80 PCR-RFLP-ITS: The sequence ITS1 5.8S rRNA ITS2 present a conserved region in the majority of yeast species and the variable regions. The primersITS1 (5'-TCCGTAGGTGAACCTGCGG-3 ') and ITS4 (5'-TCCTCCGCTTATTGATATGC-3') described as universal primers by [35]. The reaction mixture is summarized in Table 2. Then, in order to identify the different species of yeast, the products of PCR-ITS are treated with two restriction enzymes HinfI and HaeIII [3]. Table 2: The composition of the reaction mixture used for PCR-ITS according to (IFV) Products Volume (μl) Volume (μl) H2O 1220 1230 Tampon 10X 160 160 dNTP 64 64 ITS1 12,8 (40pmol ̸ reaction) 12,8 ITS4 12,8 (40pmol ̸ reaction) 12,8 Mgcl2 80 80 DMSO 31(2%) 31(2%) Purification of a DNA fragment (PCR-Delta +PCR-RFLP-ITS) double-strand is performed by electrophoresis on Agarose gel. The gel is mixed with ethidium bromide and cast hot in the electrophoresis tank. 20 μl contained in each tube PCR, mixed with 5 μl of loading buffer containing bromphenol blue, are deposited on the wells. Fragments of known molecular weight DNA called markers are also deposited: they are used to correlate the migration distance of the DNA fragments to their size (in base pairs). In this study, the number and length of the fragments were compared to the size marker (100 bp). according to (IFV).Then, applying a voltage of 120V / 30 minutes until the migration of the fragments [5].The nucleotide different bands resulting from the electrophoresis are shown on the gel under UV light (254 nm) and photographed with a camera UV. RESULTS AND DISCUSSION Isolation and purification by successive subcultures made after collection of yeasts in September 2014 from the Black Muscat grapes grown in the El Maleh area (Wilaya of Ain Temouchent). This allowed us to get a collection of 11 yeast isolates. Study cultivation of isolated yeasts: Macroscopic examination of cultures "levuriennes" after incubation at 25 ° C for 4-5 days shows generally well isolated colonies are whitish, cream or sometimes yellowish opaque and irregular outline, they have an intense smell. Microscopic observation has allowed us to identify cell shape of isolated isolates and vegetative reproduction modes. Of the 11 individual isolates, 10 are spherical or cylindrical, elongated or short form and are budding as vegetative reproduction mode. The remaining isolate is characterized by an oval shape and has a monopolar budding, it has a smell of yeast. The uniformity of cells confirms the purification of isolates studied. According to [17], yeasts are in the form of independent free single cell or combined in pairs with characteristic morphology for example: spherical, ovoid, cylindrical, apiculé, bottled, pyramidal. Molecular study of isolated yeasts: DNA extraction: DNA extraction has allowed us to observe a small white mass rushed to the microtube bottom, then it was inoculated in a buffer prior TE1x and must keep to the time of use. PCR-Delta: This technique allows to distinguish between the species Saccharomyces and Non Saccharomyces our results, the graph (Fig.1) shows that the first 10 isolates of the species Non Saccharomyces since no amplification profile is observed on their columns, so they belong to other species or they will be identified by 58 Nadia BERBER et al, 2016 Advances in Environmental Biology, 10(12) December 2016, Pages: 55-61 PCR-RFLP-ITS. Regarding the last isolate (isolate 11), we see the emergence of three bands on the different molecular size column (300 + 350 + 800 bps), then we can predict that this isolate belongs to the species Saccharomyces. The study of the ecology of Non Saccharomyces yeast known significant growth since the last few years, we focus not only on the distribution of species found on grapes but also their succession during alcoholic fermentation [1,6,20,30,32]. Many of the Non Saccharomyces yeast can colonize the surface of grape berries. Indeed, school supports the idea that although minority, Saccharomyces yeasts from the surface of the grapes, and that their presence or absence exchange of a cluster to another, within the same plot [9,19,28].[21]do consider that grape berry on 1000 carries Saccharomyces cerevisiae. However, these same authors found that damaged grapes (naturally in the vineyard) are significant populations with Bay 1 of 4 carriers of Saccharomyces cerevisiae. However, according to other authors, Saccharomyces cerevisiae is undetectable on grapes [9,28]. In our study, major yeast species were represented by Non Saccharomyces yeast (10 isolates) while only one isolate was identified as Saccharomyces(isolate 11), so our work highlights the predominance of Non-Saccharomyces species or sound samples isolated from the grape must of Muscat black grape. During a spontaneous fermentation with native flora, Non-Saccharomyces yeasts predominate in the must during the pre-fermentation stage and at the beginning of the alcoholic fermentation before the yeast S. cerevisiae colonize the middle to complete the fermentation [36,12,30]. However, Non-Saccharomyces yeasts are very present, even the majority, in the grape must (Black Muscat) compared to Saccharomyces yeasts. Fig. 1: Profils PCR-Delta of 11 isolates. Lanes M correspond to molecular size standards (100-bp DNA ladder from IFV) PCR-RFLP-ITS: A total of 11 isolates of yeasts isolated from the Black Muscat grape juice were analyzed. To identify these yeasts, the region of the rRNA repeat unit comprises two non-coding regions referred to as internal transcribed spacers (ITS1 and ITS2) and the 5.8S rRNA gene were amplified and digested by two enzymes of restriction (HinfI and HaeIII). The profiles obtained from each isolate were compared with reference strains in the determination of the IFV Guide (2012). The results of this study are summarized in Table 3. The size of the PCR products and restriction fragments of the major species identified in this study are shown in Table 4. The species of yeasts isolated from the grape (black Muscat): 11 yeast isolates were identified as belonging to 4 genera and 6 different species: Torulaspora (05 strains), Hanseniaspora (03 strains), Candida (02 strains), Saccharomyces (01 strain) (Table 3). These different kinds of yeast are well documented in the literature as present on grapes and the start of alcoholic fermentation [36,1]. Table 3: Frequency of yeast species isolated from the grape “Black Muscat” Isolation source Species Frequency of isolation(Number of strains) Black Muscat grape variety Torulaspora delbrueckii Hanseniaspora uvarum Candida solani Candida pseudointermedia Torulaspora pretoriensis Saccharomyces cerevisiae 04 03 01 01 01 01 59 Nadia BERBER et al, 2016 Advances in Environmental Biology, 10(12) December 2016, Pages: 55-61 Table 4: Size in bp of the PCR products and the restriction fragments obtained with two different endonucleases (Hinf I and HaeII)of the major species identified in this study Species Amplified product (pb) Restriction fragments (pb) Hinf I HaeII Torulaspora delbrueckii (Strains 1, 2, 3,4) 800 410+380 800 Hanseniaspora uvarum (Strains 5, 6,7) 770 350+190+160 750 Candida solani (Souche 8) 600 280+300 400 Candida pseudointermedia (Strain 9) 400 200+110 400 Torulaspora pretoriensis (Strain 10) 800 380+200+190 800 The review of the results indicates that 5 selected yeast strains (strain 1, 2, 3, 4.10) belong to the genus Torulaspora (Table 4), according to the determination of IFV guide (2012), while 4 strains were identified as belonging to the species Torulaspora delbrueckii and the remaining strain (strain 10) belongs to the species Torulaspora pretoriensis. The molecular profile of three yeast strains (strain 5, 6, 7) indicates that they look like the species Hanseniaspora uvarum, according to the determination of IFV guide (2012). However, the molecular characterization and micro-macroscopic characteristics show that the strains (8) and (9) belonging to the species Candida solani and Candida pseudointermedia respectively. Furthermore, the combination of the two results (morphological and molecular studies) indicated that the strain (11) belongs to the species Saccharomyces cerevisiae. Grape berries are the primary source of yeast during the fermentation of the must [11](Fig 2, 3, 4). In different wine regions in the world, insulation works and identification of yeasts showed that Pichia,Candida, Metschnikowia, Kluyveromyces, Cryptococcus, Rhodotorula, Debaryomyces, Issatchenkia, Zygosaccharomyces, Saccharomycodes, Torulaspora Dekkera, Schizosaccharomyces and Sporidiobolus are most frequently found [31,12,26,30,22]. Other species Non-Saccharomyces as Candida zemplinina, Torulaspora delbrueckii and Hanseniaspora spp are also an important part of the diversity of the community of the bay and are present during the fermentation, in particular during the stages pre fermentative [36]. Fig. 2: Viewing the amplified region (rRNA 5,8S ITSI-ITSII) in 11 isolates M 1 2 3 4 5 6 7 8 9 10 11 M 100 pb Fig. 3: Viewing the region (rRNA 5, 8S ITSI-ITSII) digested by HinfI in 11 isolates Fig. 4: Viewing the region (rRNA 5, 8S ITSI-ITSII) digested by HaeII in 11 isolates 60 Nadia BERBER et al, 2016 Advances in Environmental Biology, 10(12) December 2016, Pages: 55-61 In our study, the grape must (Black Muscat) is an excellent reservoir of Non-Saccharomycesyeasts as evidenced by the results obtained, we met different fermentative species such as T. delbrueckii is a non-Saccharomyces yeast naturally present in the must and the grape berries which has been described in the literature for its positive impact on the quality and complexity of wines[6,7,15] and for the purity its fermentation with especially low production of volatile acidity, acetaldehyde, diacetyl and acetoin[2,24,34]. This yeast is also described as cryophile and osmotolerant [14].Among the Non-Saccharomyces yeasts isolated from our grape must, we have the species Hanseniaspora uvarum, Candida solani and Candia pseudointermedia. Indeed yeast fermentation activity low, mainly as the species of the genus Hanseniaspora and to a lesser degree the genera Candida predominate on grapes and in the early stages of fermentation. These results are in agreement with the literature. According to[2,30,1], at the earliest stages, the Basidomycetes species are dominant, and the increasing number of Ascomycetes species, especially those that have fermentation capacity is observed at maturity stages (Metschnikowia, Hanseniaspora, Candida , Pichia). This study highlights the variability of species in each genus of yeast especially in Torulaspora genres (T.delbrueckii, T. pretoriensis) and Candida (C.Solani, C.psendointermedia). However, only one species of Saccharomyces cerevisiae was isolated from the must. This is the main agent of fermentation. Fermentations are initiated by the growth of various species of Candida, Hanseniaspora, Metschnikowia, Pichia, Schizosaccharomyces, Torulaspora, and Zygosaccharomyces. Their growth is generally limited to the first two or three days of fermentation, after which they die off. Subsequently, the most strongly fermenting and more ethanol tolerant species of Saccharomyces take over the fermentation [11]. Conclusion: This study is based on the evaluation of a grape variety grown in Algeria (Black Muscat) .A genetic approach has been developed in this work and has achieved an identification of 11 isolates belonging to 4 genera and 6 different species: Torulaspora, Hanseniaspora,Candida and Saccharomyces. This variety is an excellent tank of Non Saccharomyces yeasts as evidenced by the results. 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Rational selection of non-Saccharomyces wine yeasts for mixed starters based on ester formation and enological traits.Food Microbiology, 25:778-785. [35] White, T.J., T. Bruns, S. Lee and J. Taylor, 1990. Analysis of phylogenetic relationships by amplification and direct seq uencing of ribosomal RNA genes tiré de PCR Protocols: A guide to Methods and Applications. M. A. Innis, D. H. [36] Zott, K., C. Miot-Sertier, O. Claisse, A. Lonvaud-Funel and I. Masneuf-Pomarede, 2008. Dynamics and diversity of non-Saccharomyces yeasts during the early stages in winemaking.International Journal of Food Microbiology, 125: 197-203. | en_US |
| dc.subject | Mots clés: Raisin, Levures, Saccharomyces cerevisiae, PCR-Delta, PCR-ITS-RFLP, Invertase..-Key words: Grape, Yeasts, Saccharomyces cerevisiae, PCR-Delta, PCR-RFLP-ITS, Invertase..-:: | en_US |
| dc.title | Caractérisation biomoléculaire et biotechnologique des souches de « Saccharomyces cerevisiae » issues des cépages Algériens | en_US |
| dc.type | Thesis | en_US |
