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    • 专利摘要:
    Recombinant strain, method of production of aspartic proteases of Galium verum and use in the dairy industry. Construction of a recombinant strain that overexpresses vegetable aspartic proteases of the species Galium verum used as vegetable coagulants, procedure for obtaining and using these coagulants in the dairy products industry. (Machine-translation by Google Translate, not legally binding)
    公开号:ES2673702A1
    申请号:ES201631665
    申请日:2016-12-23
    公开日:2018-06-25
    发明作者:Tomás GONZÁLEZ VILLA；Lucía FEIJOO SIOTA；José Luis RODRÍGUEZ RAMA；Trinidad DE MIGUEL BOUZAS
    申请人:Universidade de Santiago de Compostela；
    IPC主号:
    专利说明:

    DESCRIPTION

    RECOMBINING CEPA, METHOD OF PRODUCTION OF ASPARTIC PROTEASES OF GALIUM VERUM AND USE IN THE MILK INDUSTRY.
     5
    TECHNICAL SECTOR OF THE INVENTION
    The present invention is within the field of biology and biotechnology. It refers to the use of recombinant DNA technology for the production of industrial proteins. More particularly, the present invention relates to cells or microorganisms containing polynucleotides derived from the plant species Galium verum, which encode aspartic proteases, and the production of aspartic proteases for industrial use.
    STATE OF THE TECHNIQUE
    Coagulation of milk by enzymes is a basic step in the manufacture of most cheeses. Milk mainly contains two types of proteins: the 15 caseins, which precipitate during the coagulation process, and whey proteins, which remain soluble; of the protein fraction only caseins will constitute the cheese. Caseins constitute approximately 80% of milk proteins and there are mostly four types: αs1-, αs2-, β- and κ-caseins. These proteins are part of spherical structures called 20 micelles, on whose surface are the κ-caseins, which are those that give stability to the structure.
    All enzymes (rennet and coagulants) used industrially for cheese making belong to the group of aspartic proteases (PAs) (EC 3.4.23) and hydrolyze the k-casein in the Phe105-Met106 bond. 25
    The milk coagulation process consists of two phases, in the first phase, the PAs hydrolyze the Phe105-Met106 junction of the k-casein by dividing the protein molecule into two: hydrophobic para-k-casein and a hydrophilic part known as caseymacropeptide ; In the second phase, the coagulation of the micelles of the caseins that were destabilized by the proteolytic attack occurs. 30
    The type of coagulant used in cheese making has a great influence on the organoleptic characteristics of the final product.
    The rennet and coagulants currently used can be classified into four types: animal rennet (chymosin), microbial PAs of Rhizomucor miehei, Rhizomucor pusillus or Endothia parasitica), fermentation produced chymosin (FPC: fermentation produced chymosin) in yeasts (Saccharomyces cerevisiae and kluyveromy lactis) and fungi (Aspergillus niger) and vegetable coagulants (Kumar et al. 2010). These PAs 5 are produced as inactive precursors, which are converted into active enzymes by autocatalytic division of the N-terminal part called the propeptide.
    Within the category of vegetable coagulants are aqueous extracts of flowers of different species of the Cynara genus, whose pistils express a large number of PAs. The basic investigations carried out on these PAs and the 10 belonging to other plant species, have revealed that the primary structure of most of the PAs of plants that have been characterized is similar to that of mammals and microorganisms and includes: a signal peptide in the amino terminal end, a propeptide involved in inactivation or in the correct folding, stability and cell signaling and a fragment known as plant-specific insert 15 (PSI) located between the amino and carboxy terminal end, which comprises approximately 100 amino acids and maintains its structure thanks to three disulfide bridges. PSI has only been identified in plants and is similar to the precursor of mammalian saposins, its biological function has not been fully established.
    Plant PAs are synthesized as inactive precursors and converted into active enzymes by processing involving several proteolytic steps. The processing includes the removal of the signal peptide and the propeptide, resulting in a heterodimeric or monomeric enzyme. The heterodimeric PAs are constituted by a heavy chain (HC) and a light chain (LC) that remain linked by hydrophobic interactions, hydrogen bonds or disulfide bridges, the processing of these PAs to their active form generally includes total or partial elimination of the PSI. The removal of the propeptide for the enzyme to be active may be triggered by accessory molecules or require a decrease in pH (Simoes and Faro, 2004).
    Formerly, plant extracts were used for the manufacture of cheese that contained various PAs, some are still used locally today, such as the berries of the Solanum dobium plant or several papilionoideae species that have been used to make a traditional cheese in Sudan “Jibna beida” and other dairy products in Angola (Kheir et al. 2011); the juice extracted from Calotropis procera (apple of sodoma) that is used in regions of Nigeria and Benin; in the south of 35
    China ginger root is used to produce a kind of "tofu" much appreciated. Other plants that have been investigated as a source of proteases are: seeds of Balanites, Solanum, albizia, asparagus and fruits such as kiwi and melon (Mazorra-Manzano et al. 2013).
    Many of the plant extracts that have been studied so far are not useful in the manufacture of cheeses since they have a high proteolytic activity in relation to their coagulant activity, which results in a too rapid clot hydrolysis, causing a reduction in the Defective production and / or cheeses due to the bitterness generated by hydrophobic peptides released at maturation. Other drawbacks of the use of vegetable coagulants 10 are: the cost of collecting and processing plant material and the standardization of the coagulant force between lots. However, others such as the aqueous extracts of the flowers of Cynara cardunculus, C. humilis and C. scolymus, whose pistils express a large number of PAs (Sarmento et al. 2009) have shown to be good milk coagulants and are used Nowadays, at an artisanal level 15 in several areas of Spain and Portugal for the manufacture of goat and sheep cheeses such as Casar de Cáceres, Torta del Casar, La Serena, Los Ibores, Serra da estrela or Flor de Guía (Harboe et al ., 2010).
    The use of these alternative coagulants favors the obtaining of cheeses different from those we usually find in the market, this is because the majority of 20 PAs of plants break the α-, β- and k-caseins, while the animal chymosin Normally used for cheese production only breaks the kappa casein. PAs of the species Cynara cardunculus have been expressed in different microorganisms and their properties have been studied as vegetable coagulants of milk: cyprosin B (Sampaio et al., 2008)) and cardosin B (Almeida et al. 2015). The production of plant PAs using microorganisms allows their obtaining in large quantities, without dependence on the time of flowering or the need for storage of the plant material and the possibility of standardizing the coagulant obtained, thus eliminating the inconvenience of the use of extracts obtained from the plant. 30

    DESCRIPTION OF THE INVENTION
    The plant species Galium verum, whose scientific name refers to its coagulant capacity (in Greek gala, galaktos means milk), also known as "cuajaleches" contains in its genome at least two genes that code for 35
    PAs which have been called preprogaline A (GenBank: AFX73038.1) and preprogaline B (GenBank: AFX73039.1) (Feijoo-Siota et al. 2012). These aspartic proteases could be used in the elaboration of dairy products, especially cheeses and in their accelerated maturation due to the hydrolysis pattern of the milk caseins they present. Like the proteases of the species 5 Cynara cardunculus could also be used in the production of dairy products with bioactive peptides (Silva et al. 2006),
    The present invention relates to a recombinant strain for the production of recombinant PAs of the species Galium verum that have been deposited in the Spanish Type Culture Collection (CECT), with the number CECT 13141, method of production and use in industry milky This recombinant strain secretes the enzyme to the culture medium where it is activated, due to this and because the yeast used as a host secretes few endogenous proteins to the culture medium, the process for obtaining and purifying it is simple. The recombinant aspartic protease described herein has milk coagulant activity and its cutting pattern on caseins 15 differs from the animal, microbial or vegetable coagulants currently used for the manufacture of dairy products. According to this, aspartic protease could produce cheeses with novel characteristics.

    Therefore, in a first aspect, the invention relates to a vector comprising a polynucleotide with the nucleotide sequence shown in SEQ ID NO: 1 or in SEQ ID NO: 2, or a variant thereof having a degree of identity of at least 80% with respect to said SEQ ID NO: 1 or SEQ ID NO: 2, or sequences included in SEQ ID NO: 1 or in SEQ ID NO: 2 encoding peptide fragments of PAs Galium verum that maintain the breakage properties of α-, β- and κ-caseins and that encode a peptide with aspartic protease activity of the plant species Galium verum.

    In this specification, the percentage of nucleotide sequence identity is understood as the percentage of coincidences of the same nucleotides between two aligned sequences, along the entire length of both sequences.

    In another aspect, the invention relates to a cell or microorganism comprising said vector, or the peptide encoded by said vector, where the host cell or microorganism is transfected or transformed with the vector and cultured under conditions that promote expression and recovery. of the peptide.

    This specification refers to conditions that promote the expression and recovery of the peptide as those conditions of culture medium, temperature, pH and incubation time necessary for the correct expression of the polynucleotide to be obtained obtaining the protein in its active form or 5 inactive.

    On the other hand, the invention also relates to a cell or microorganism that has integrated in its genome the polynucleotide with the nucleotide sequence shown in SEQ ID NO: 1 or in SEQ ID NO: 2, or a variant thereof having a degree of identity of at least 80% with respect to said SEQ ID NO: 1 or SEQ ID NO: 2, or sequences encoding peptide fragments of aspartic proteases of Galium verum that maintain the breakage properties of α -, β- and κ-caseins and encoding a peptide with aspartic protease activity.
     fifteen
    On the other hand, the invention also relates to a method for producing PAs that consists of culturing the cell or microorganism that contains a vector or has integrated in its genome the polynucleotide with the nucleotide sequence shown in SEQ ID NO: 1 or in SEQ ID NO: 2, or a variant thereof that has an identity degree of at least 80% with respect to said SEQ ID NO: 1 or SEQ ID 20 NO: 2, or sequences encoding peptide fragments of Galium verum PAs that maintain the breakage properties of α-, β- and k-caseins and that encode a peptide with aspartic protease activity when incubated in a culture medium at a pH, temperature and agitation that promote expression and recovery of the peptide.
     25
    On the other hand, the invention relates to a method for producing PAs in their inactive form by obtaining them from the culture of the cell or microorganism that contains a vector or has integrated into its genome the nucleotide sequences mentioned above by their culture in a buffer medium at basic pH. These PAs can be activated before use by incubation at acidic pH. 30

    On the other hand, the invention also relates to the use of the coagulant obtained directly from a host cell or microorganism transformed or transfected with the vector or that have integrated the polynucleotide into its genome, for the coagulation of milk, of milk mixtures of different animal origin or 35 drinks partly made up of milk.

    On the other hand, the invention also relates to the use of the coagulant obtained directly from a host cell or microorganism transformed or transfected with the vector or that have integrated the polynucleotide into its genome mixed with other coagulants, for the coagulation of milk, of mixtures of milk of different animal origin or beverages partly composed of milk. 5

    In this specification, milk is understood as the product obtained from the females of mammals, in particular domestic mammals such as cow, goat, sheep, camel, buffalo, dromedary, mare, etc. Coagulation can be carried out in the types of milk described herein or in any of their mixtures. 10

    Another preferred embodiment of the present invention comprises the use of the active recombinant coagulant of Galium verum for the manufacture of dairy products, where dairy products can be obtained from any type of milk, mixtures or beverages partly composed of milk , more preferably for cheese making.
    In this specification an active recombinant coagulant is understood as an aspartic protease of plant origin produced in a host organism transformed with the DNA encoding said protease and having the ability to produce enzymatic coagulation of milk without the need for a process of 20 previous activation.

    DESCRIPTION OF THE FIGURES

    Figure 1. RACE PCR from the complementary DNA of G.verum. Products 25 were separated on a 1% agarose gel. Line 1: 5´RACE performed with the oligonucleotides (AP1 / pMgv2r) and line 2: 3´RACE (pMgv2f / AP1). Line 3 corresponds to the molecular weight marker.
    Figure 2. Schematic representation of the preprogaline B protein encoded by the gv2AP gene. Signal peptide (SP); propeptide (Pro); N-terminal domain with two catalytic sites (DTG and DSG); plant specific insert (PSI) containing two type B saposin domains (Sap_B2 and Sap_B1) and C-terminal domain; the fork symbol indicates an N-glycosylation site; Connected lines indicate predicted disulfide bridges (S-S). The triangle indicates the region of the protein against which the PV13 antibody used in Western blots was generated. 35
    Figure 3. Expression vector pGAPZα - gv2AP used to obtain the strain of Pichia pastoris producing progaline B (CECT13141). Construction was performed using the EcoRI and XbaI restriction sites so that the signal peptide of the gv2AP gene was replaced by the α factor carrying the vector and under the control of the constitutive promoter pGAP and the transcription terminator of the AOX1 gene ( AOX1TT). The construction was linearized by the BspHI restriction enzyme and integrated into the Pichia genome by homologous recombination.
    Figure 4. Analysis of the expression of recombinant progaline B in the supernatant of P. pastoris concentrated by precipitation with TCA. A / 10 SDS PAGE. Lines 2-4: Supernatants of the recombinant strain producing progaline B after 1 day, 2 days and 3 days of culture. Lines 5-7: Supernatant of the untransformed strain (negative control) after 1 day, 2 days and 3 days of culture. B / Western Blot. The supernatant from a 3-day culture was analyzed using loading buffer with (line 2) and without (line 3) β-mercaptoethanol using an antibody 15 (fig. 2 PV13) generated against a heavy chain peptide of progaline B Progaline B bands are indicated by arrows (HC: heavy chain; LC: light chain; glyc: glycosylated)

    Figure 5. Western blot analysis performed on the supernatant of the culture medium of the recombinant strain. Progaline B before (line 2) and after (line 1) being treated with endoglycosidase H. Samples were prepared without reducing agent (β-ME) in the loading buffer. M: biotinylated marker (Sigma B2787).
    Figure 6. Growth curve (- ● -) and enzymatic activity (−▪−) of the supernatant of the P. pastoris strain producing progaline B (CECT13141). The strain was incubated in YPD medium at a temperature of 28 ° C and stirring of 230 rpm for 195 h; The graph also shows the variation in the pH of the medium (… x…). The data presented in the graph represent the average of three measurements made on three different flasks. The incubation time with FTC-k-casein to determine the enzymatic activity was 2 hours. 30
    Figure 7. SDS-PAGE analysis of the proteolytic activity of progaline B and commercial coagulants on κ- (A /), α- (B /) and β- (C /) caseins for 2 hours at 35 ° C. Line 1 molecular weight marker. In all figures, line 2 corresponds to the hydrolysis of casein by progaline B incubated with pepstatin, lines 3-9 degradation of caseins with the following coagulants: (3) 35
    progaline B, (4) calf chymosin, (5) bovine chymosin produced by fermentation, (6) calf rennet, (7) adult bovine rennet, (8) microbial coagulant, (9) camel chymosin produced by fermentation. Line 10 corresponds to the κ-, α- and β-caseins incubated 2 hours at 35 ° C without any coagulant.
    Figure 8. Effect of temperature and pH on the activity of progaline B. 5 Left: the optimum temperature of semi-purified progaline B was determined using FTC-k-casein as a substrate in 100 mM sodium acetate buffer at pH 5.5 at temperatures incubation in the range of 4 to 80 ° C for 1 hour. Right: the optimum pH was determined using 1% azocasein as a substrate dissolved in a 100 mM concentration of buffers at pHs in the range (4.4-7) for 2 hours at 37 ° C. The relative activity is expressed as a percentage of the highest activity at the temperature (left) or pH (drch) examined.
    Figure 9. Effect of the pH of the culture medium in the processing of progaline B secreted by Pichia pastoris after three days of culture at 28 ° C. A / Western blot of the supernatants of the recombinant strain grown in YPD, YPD 15 buffered to pH 7 (YPD7) and YPD buffered to pH4 (YPD4). B / The pH of the supernatants shown in A was adjusted to pH 3.5 with HCl and incubated 4.30 hours at 37 ° C. Samples were prepared in the presence (+) or absence (-) of reducing agent in the SDS PAGE loading buffer. C / Activities of the supernatants of the recombinant strain and the untransformed strain (negative control) in YPD, YPD4 and 20 YPD7 before (C.1) and after (C.2) the pH drop. The incubation time with FTC-κ-casein was 1.30 hours. The values shown are the average activity with the standard deviation obtained from three measurements.
    Figure 10. Effect of pH on the activation of recombinant progaline B. A / The recombinant P. pastoris strain was grown in YPD buffered at pH7 (YPD7) 25 for 72 hours. The culture was centrifuged, a 0.2 M buffer volume at different pHs 3.5, 4.3, 4.6, 5.0, 5.8, 6, was added to aliquots of the supernatant (A / line 1). 6 and 7 (lines 2-8 respectively) and incubated at 28 ° C. Samples taken after 30, 150 and 270 minutes were analyzed by Western blotting under reducing conditions (A.1, A.2 and A.3 respectively). B / Activity on k-30 casein of supernatants incubated 270 minutes at different pHs. The pH of all samples was adjusted to 5.5 by the addition of NaOH or HCl before adding the FTC-k-casein and the incubation time was 2.30 hours. EMBODIMENT OF THE INVENTION

    The present invention is adequately illustrated by the following examples, which are not intended to be limiting in scope. 5

    Example 1. Obtaining the gene sequence coding for the aspartic proteases preprogaline A and preprogaline B from Galium verum
    To obtain the gene sequence of the PAs referred to in this invention, two oligonucleotides, pAPF (sense) and pAPR (antisense), were designed (table 1), based on two conserved regions of gene sequences deposited at the base of Genbank data, which code for vegetable aspartic proteases (Laloi et al. 2012). These oligonucleotides were used to perform a RT-PCR, using total RNA extracted from the flowering plant Galium verum (RNeasy Plant Mini Kit, Qiagen). The BioScript MMLV enzyme (Bioline) was used to synthesize the first strand of complementary DNA following the manufacturer's recommendations. The RT-PCR reaction mixture (50 µl) consisted of 4 µl of complementary DNA, 3.75 units of Accuzyme DNA polymerase (Bioline), 1mM dNTPs, 10 pmol of each primer (pAPF and pAPR) and the program of amplification consisted of 30 cycles at a hybridization temperature of 46 ° C. The amplification products were analyzed by agarose gel electrophoresis, obtaining a band of the expected size (approximately 1 kb) that was purified (Gel band Purification kit; GE Healthcare) from the gel and the DNA obtained was cloned into the vector pCR Blunt II TOPO using the Zero Blunt TOPO PCR Cloning kit (Invitrogen). Plasmid DNA was extracted from several colonies obtained in the transformation and sequencing was performed using the universal oligonucleotides SP6 and T7.
     Thus, two partial sequences of G. verum aspartic proteases were obtained from which the specific oligonucleotides pMgv1f / pMgv1r were designed to obtain the complete nucleotide sequence of the gene that we will call gv1AP that codes for preprogaline A aspartic protease (access code: AFX73038.1) and the oligonucleucleotides pMgv2f / pMgv2r to obtain the sequence of the gv2AP gene encoding the preprogaline B aspartic protease (access code: AFX73039.1). The nucleotide sequence of the oligonucleotides used is in table 1. The RACE PCR reactions were carried out following the instructions of the Marathon® cDNA Amplification kit (Clontech). The sequence coding for end 35
    N-terminal (5'RACE PCR) was obtained using the oligonucleotide pair AP1 / pMgv1r in the case of the gv1AP gene and AP1 / pMgv2r in the case of the gv2AP gene; the C-terminal (3'RACE PCR) end by the oligonucleotide pair pMgv1f / AP1 for the gv1AP gene and pMgv2f / AP1 for the gv2AP gene. The PCRs were developed on double stranded DNA in 50 µL volumes with the Accuzyme 5 DNA polymerase (Bioline) and the amplification program (94 ° C, 30s) 1x (94 ° C 5s, 72 ° C 3 min) 30x (72 ° C, 7min) 1x.
    Table 1. Sequences of oligonucleotides.
     Description  Name of the oligo Sequence (5-3´)
     Degenerate sense primer  pAPF GAYACNGGNAGYTCYAAYYTVTGG *
     Degenerate reverse primer  pAPR CCATMAANACRTCNCCMARRATCC *
     Marathon AP1 Primer  AP1 CCATCCTAATACGACTCACTATAGGGC
     gv1AP (3´RACE)  pMgv1f CAGGGGTTTCACCTGACAAGGTCTGCGC
     gv1AP (5´RACE)  pMgv1r GCCATCTGGCAAGCAGAACACATCGGTG
     gv2AP (3´RACE)  pMgv2f GTTCTGCTATTGCCGACTCTGGAACTTC
     gv2AP (5´RACE)  pMgv2r TTGGCTCACAACACCAGTAGCTCCA
     pGAPZαA sense  pGV2-EcoRI CCGAATTCTCCGCAGCTTTGTTATCAGCATCTG
     pGAPZαA reverse  pGV2-XbaI GCTCTAGATCAAGCTGCTTCTGCGAATCCAACCC

    * Y = C, T; R = A, G; V = A, G, C; M = A, C; N = A, C, G, T 10
    The amplified fragments were cloned using the Zero Blunt TOPO PCR Cloning kit (Invitrogen) and sequenced. The sequences at both ends were assembled using the VectorNTI software, thus obtaining the complete sequence of two gv1AP (Genbank: JQ434478.1) and gv2AP (Genbank: JQ434479.1) genes that code for aspartic proteases preprogaline A and 15 preprogaline B respectively . A schematic representation of the preprogaline B is shown in Figure 2.

    Example 2. Construction of the expression vector pGAPZα-gv2AP.
    For the expression of preprogaline B without the signal peptide (which we will call progaline B) in the yeast Pichia pastoris X-33 (GRAS), the integrative vector pGAPZαA (Invitrogen) was used. This vector contains the constitutive promoter pGAP, a sequence that codes for the signal peptide of the Saccharomyces cerevisiae 5 factor that allows the extracellular secretion of the enzyme, the terminator of the AOX1 gene and the zeocin resistance gene.
    For the construction of pGAPZα-gv2AP (fig. 3) a pair of oligonucleotides pGV2-EcoRI / pGV2-XbaI (table 1) were designed to amplify the gv2AP gene without the signal peptide thereof and introduce the appropriate restriction targets for its use. introduction into the vector pGAPZαA in order to clone the gene in reading pattern with the signal peptide (factor α) of S. cerevisiae carrying the vector. The PCR reaction to amplify the gene fragment was carried out with 1.25 U PrimeSTAR® HS DNA Polymerase (Takara) using the buffer supplied therewith supplemented with 200 µM of each dNTP; 0.3 µM oligonucleotides (pGV2-15 EcoRI / pGV2-XbaI) and complementary DNA obtained using the High Fidelity cDNA Synthesis (Roche) Transcription Kit in a final volume of 50 µl following a program of: 98ºC 10s, 58ºC 5s, 72ºC 1, 40 min for 30 cycles. The PCR product was purified from a 1% agarose gel and digested with the restriction enzymes EcoRI and XbaI. The pGAPzαA vector was digested with the same enzymes and fragments 20 were ligated with ligase enzyme (Takara) overnight at 16 ° C. Competent E.coli TOP10 cells were transformed with the construction obtained and selected using the Zeocin resistance marker carrying the vector. The pGAPZα-gv2AP vector was purified from E. coli by the Plamid Midiprep kit (Qiagen) and used for the transformation of P. pastoris. 25
    Example 3. Transformation of Pichia pastoris X-33 with pGAPZα-gv2AP.
    The transformation of the P. pastoris X-33 strain was carried out following the instructions in the pGAPZα A, B, and C (Invitrogen) manual. Thus, the vector pGAPZα-gv2AP was linearized with the restriction enzyme BspHI, after which the enzyme was inactivated 20 min at 65 ° C and the DNA was cleaned by chloroform phenol. 9 µg 30 of the linear pGAPZα-gv2AP construct were obtained which were introduced into Pichia pastoris cells by electroporation: a Gene Pulser® II electroporator (BioRad) was used, the electroporation cuvette was 0.2 cm (BioRad) and the pulse of 25uF, 200 Ω and 1.8 kv. Linear fragments were integrated into the genome of Pichia pastorís through homologous recombination events, this integration can occur in 35
    several copies, as a result, strains that synthesize the enzyme can be obtained stably and in large quantities. Colonies were selected on YPDS plates (1% yeast extract, 2% peptone, dextrose, 1M sorbitol, 2% agar) supplemented with 100 µg / ml zeocin. The integration of the expression cassette into the Pichia genome was confirmed by PCR using as template the genomic DNA extracted with the Epicenter MasterPure kit and with the oligonucleotides pGAP (GTCCCTATTTCAATCAATTGAA) and 3´AOX1 (GCAAATGGCATTCTGACATCC).
    Example 4. Analysis of the production of progaline B by recombinant P. pastoris.
    An assay was conducted to determine the ability to hydrolyze the kappa casein of the clones that had integrated the cassette into their genome using k-casein labeled with fluorescein isothiocyanate (FTC-κ-casein) following the method of Ageitos et al. 2006. The selected clones were grown in YPD medium at a temperature of 28 ° C and agitation 230 rpm; The untransformed strain was grown under the same conditions to be used as a negative control. The cultures were centrifuged and the supernatants stored at -70 until their caseinolytic kappa activity was measured. The reaction mixture was performed in an eppendorf tube and contained 10 µL of the supernatants obtained at different culture times, 4.2 µL of FTC-k-casein and 50 µL of 0.1M sodium acetate buffer, pH 5.5. Incubation was performed at 37 ° C for 2 hours in the dark. The reaction was stopped by adding 120 µL 20 of 5% cold TCA. Once the reaction was stopped, it was maintained for a minimum of one hour at room temperature protected from light. The vials were centrifuged at 4 ° C and 18000g for 10 min and 50 µL of the supernatant was mixed with 350 µL of 0.5 M Tris-HCl 500mM, pH 8.5 on a plate. Fluorescence in a Perkin Helmer Luminescence Spectrometer LS50B fluorimeter with an excitation λ of 490 nm and an emission of 525 nm. The strain that showed the highest proteolytic activity of k-casein was selected and grown in YPD at 28 ° C, 230 rpm. The supernatant of this strain was analyzed after 72 hours of culture by 12% SDS PAGE and Western Blot (fig. 4). As a primary antibody to perform Western Blot, a rabbit-produced polyclonal antibody was used against a synthetic 1330 amino acid peptide (PSHFKGEHVYAKV) whose sequence corresponds to amino acids 243-255 of preprogaline B (GenBank: AFX73039.1).
    In the analysis by SDS PAGE of the culture supernatant of the recombinant strain it is observed that as of the second day of culture a band of 30.7 kDa appears that does not appear in the supernatant of the strain without transforming (Fig. 4A). 35 In the Western Blot two bands of 51.2 kDa and 46 kDa were observed when
    loading buffer was not added β-ME (fi. 4B line 3), while a single band of 30.7 kDa appeared when the loading buffer contained the reducing agent (fig. 4B line 2). This confirms the structure predicted by different bioinformatic programs and by homology with other aspartic proteases of plant origin. Progaline B is secreted by P. pastoris yeast to the culture medium and undergoes proteolytic processing so that the propeptide and part of the PSI are eliminated giving rise to a protein formed by two chains linked by disulfide bridges (bands 51.2 and 46 kDa) in which the heavy chain (HC) would be attached to the light chain (LC) by disulfide bridges; Progaline B would be secreted in glycosylated form (51.2 kDa band) and non-glycosylated (46 kDa band) (verified by 10 deglycosylation test, the results of which are shown below). When we add β-ME to the loading buffer, we only detect the heavy chain (30.7 kDa), since the disulfide bonds that bind both units are broken and the antibody used (PV13) recognizes a peptide that is located in the heavy chain ( figure 2). fifteen
    The progaline B-producing strain has been deposited according to the Budapest Treaty in the CECT (Spanish Type Culture Collection) with the registration number CECT13141.

    Example 5. EndoH deglycosylation of progaline B expressed in Pichia 20 pastoris.
    Progaline B was incubated with endoglycosidase H to check whether the two bands observed when Western Blot was performed on samples to which β-ME was not added were due to the presence of a predicted N-glycosylation site at the end of the PSI region (fig. 5). Deglycosylation was performed by incubating 10 µl of the supernatant of the 25 recombinant strain grown for 3 days in YPD medium at 28 ° C and 230 rpm and concentrated 20 times with 2 µl of endoglycosidase H (1U / mL) of Streptomyces griseus (Sigma) in 50mM buffer pH5 phosphate in a final volume of 50 µl; 2ml of milliQ water was used as a negative control instead of endoH. After incubating 4 hours at 37 ° C the reaction was stopped by adding 10 µl of SDS-30 PAGE loading buffer without β-ME to 10 µl of the samples, the mixture was heated at 95 ° C 7 minutes and analyzed by Western Blot.
    Through this test, it was confirmed that progaline B is secreted by P. pastoris in two forms, one glycosylated and one non-glycosylated (fig. 5, line 2, bands 51.2 and 46 kDa),
    when progaline B is treated with endoH we see how only one band appears (the deglycosylated form, fig. 5, line 1).
    Example 6. Production of small scale progaline B.
    An assay was performed to determine the incubation time to obtain the maximum amount of active progaline B in the supernatant of the YPD 5 culture medium (1% yeast extract, 2% peptone, 2% dextrose). 100ml of medium was used in 500 ml flasks with an initial inoculum so that the OD600 was 0.02 and the culture conditions were 28 ° C and 230 rpm. Growth was analyzed by measuring absorbance at 600 nm using a Beckman DU-640 model spectrophotometer (DO600); Enzymatic activity using FTC-κ-casein using the method of Ageitos et al., 2006 and the variation of pH in the culture medium (fig. 6).
    The activity was maximum after 70-92 hours of cultivation, in the stationary phase of growth, then the activity decreased progressively. The activity of the supernatants of a culture from the untransformed strain of P. pastoris (negative control) was close to zero in all the samples analyzed. The pH of the YPD culture medium changed with the growth of the yeast, initially it was 6.4 and it decreased to a value of 4.6 after 27 hours of incubation, then gradually increased to 7.58 after 195 h of incubation

    Example 7. Hydrolysis of bovine milk caseins. twenty
    The degradation pattern of caseins is an important factor when evaluating a new coagulant because this pattern can affect the performance, texture and evolution of proteolysis during cheese maturation.
    To analyze the cut-off pattern of caseins, commercial bovine α-casein, β-casein and κ-casein (Sigma-Aldrich) dissolved in 100 mM sodium phosphate pH 6 25 were used at a final concentration of 1 mg / ml and incubated independently with 20 µl of each of the following coagulants: semi-purified progaline B by DEAE-BioGel A, microbial coagulant produced by Rhizomucor miehei Mucorzyme “L” (Biostar SA), calf chymosin (Sigma R4877) Chymax P (bovine chymosin) and Chymax M (camel chymosin) produced in Aspergillus niger var. awamori, 30 (CHR Hansen), calf and Bovine REMCAT Standards for rennet testing, CHR Hansen.
    The volume of coagulants used in the assay was calculated so that they all had the same strength. Strength (SU) was defined as the number of coagulated milk volumes per coagulant volume in 40 minutes at 35 ° C. 35
    SU = 2400V / tv, where v is the coagulant volume (ml), V milk volume (ml) and t the coagulation time in seconds. The milk used in the test was 10% Nestle Sveltesse skimmed milk powder supplemented with 10mM CaCl2 at pH 6. The coagulation time was determined visually. Thus the added volume of each coagulant was calculated by applying the formula v = 0.120 / SU and water was added to a final volume of 20

    l.
    As a negative control, semi-purified progaline B was incubated in the presence of pepstatin A (aspartic protease inhibitor) at a final concentration 2
    µ
    M for 30 min at 37 ° C before adding the α-, β- or κ-casein; a white was also made with water.
    10
    The reaction with the different caseins was carried out at 35 ° C for 2 hours after which the reaction was stopped by adding to a sample volume a volume of loading buffer (200 mM Tris-HCl, pH 6.8, 40% glycerol, 2% SDS, 0.04% Coomassie Blue G-250, 2% β-ME) and heating at 95 ° C for 7 minutes.
    The samples were analyzed by SDS-PAGE 16.5% according to the method of Laemmli 15 but using as Tris-Tricine electrophoresis buffer (100mM Tris, 100mM Tricine, 0.1% SDS). The proteins were fixed with a methanol / acetic acid / water solution (4: 1: 5); stained with 0.025% (w / v) Coomassie Brilliant Blue G-250 (Bio-Rad) in 10% acetic acid and stained with 10% acetic acid.
    The hydrolysis of bovine α-, β- and κ-caseins using progaline B and several commercial coagulants is shown in Figure 7. The cut pattern of progaline B on k-casein has the same specificity as the rest. of the commercial coagulants normally used for cheese making (fig.7A lines 3-9). The digestion of k-casein results in the appearance of a product of about 13.5 kDa that would correspond to the expected molecular weight for para-k-casein that results from hydrolysis in the Phe105-Met106 bond that triggers the process of milk coagulation. These bands are not observed in the k-casein to which no coagulant has been added (fig7A line 10), nor to which it has been incubated with progaline B treated with pepstatin (fig7A line 2).
    The proteolytic activity of progaline B on α- and β-caseins is greater than that of the coagulants tested. Thus we can observe how when progaline B is incubated with α-casein (fig.7B, line 3) or β-casein (fig.7C, line 3) for 2 hours the hydrolysis pattern is greater than that generated with the rest of coagulants
    This test indicates that progaline B hydrolyzes k-casein just like the rest of coagulants used today for cheese making and that it has a higher proteolytic activity on α- and β-caseins than these.
    Example 8. Optimum temperature and pH
    To determine if progaline B had adequate characteristics to be used as a milk coagulant for cheese making, its optimum temperature and pH were determined.
    The optimum temperature was determined by measuring the activity on FTC-κ-casein according to the method of Ageitos et al. 2006. Semi-purified progaline B was used by DEAE Biogel A column and as a buffer 100 mM sodium acetate at pH 5.5. The temperature at which progaline B exhibits the highest activity on k-casein under these conditions was 50 ° C, with 50% and 69% relative activity respectively between 30 ° C and 35 ° C (usual temperatures in cheese making).
    To analyze the optimal pH: 20
    µ
    l of semi-purified progaline B were incubated with
    15 480

    l 1% azocasein solution (Sigma) using a 100 mM concentration of buffers at different pHs (4.4-7) for 2 hours at 37 ° C: the buffer used in the pH range 4.4 to 5.6 was sodium acetate buffer and phosphate buffer sodium in the range 6.0-7.0. The optimal pH of progaline B was observed at pH 5, the activity was lower when the buffer was more alkaline, so at pH 7 only 20 21.7% of the activity was preserved. The values are similar to those obtained for aspartic proteases of the plant species Cynara cardunculus used for cheese making (Sampaio et al., 2008; Almeida et al. 2015). Chymosin has an optimal milk coagulation temperature at pH 6.6 approx. 45 ° C and an optimum pH between 3.5-5.5 depending on the substrate used for the analysis. 25
    Example 9. Milk coagulation using recombinant progaline B.
    The supernatant from a 3-day culture of P. pastoris expressing progaline B was concentrated 50 times and 50 µl was added to 1 ml of milk (12% (w / v) skimmed powder (Nestle Sveltesse) supplemented with 10mM CaCl2, pH 6 at 37 ° C in glass tubes and the time that elapsed until the first 30 flocs appeared.The negative controls were used: distilled water, progaline B incubated with pepstatin A at a concentration of 2 µM at 37 ° C for 30 minutes and the supernatant of a strain of P. pastoris untransformed obtained under the same conditions as the transformed strain. The time elapsed until the appearance of the
    First flocs was 35 minutes. It was also found that progaline B coagulated cow and sheep milk, the clot being firmer and requiring a shorter coagulation time when sheep origin was used.
    Example 10. Influence of the culture medium for the production of progaline B in its active or inactive form. 5
    The recombinant strain of P. pastoris was grown at 28 ° C and 230 rpm for 3 days in YPD medium, YPD medium adjusted to pH7 by means of sodium phosphate buffer (named YPD7) and in YPD medium adjusted to pH4 by citrate buffer (named YPD4) at a 100 mM final concentration of each of the buffers. The untransformed strain was grown under the same conditions to verify that the proteolytic activity 10 was not due to possible proteases secreted by P. pastoris.

    The pattern of bands in the Western blot of progaline B when the recombinant strain was grown in YPD4 (fig. 9 A /, lines 1 and 2) or YPD (fig. 9 A / lines 5 and 6) was the same, both under reducing conditions (+) as non-reducing (-) (described in example 4). When the strain was grown in YPD7, progaline B had a molecular weight of 56 kDa under reducing conditions (fig. 9 A / line 3), which corresponds to the predicted molecular weight for the unprocessed enzyme form (with the propeptide and the PSI present). The difference in the molecular weight of the protein under non-reducing conditions (58 kDa, fig. 9 A /, line 4) could be due to the form adopted by it when the disulfide bridges are not broken. Progaline B secreted in YPD and YPD4 shows proteolytic activity using FTC-κ-casein as a substrate, while that produced in YPD7 is inactive (Fig. 9 C1). The conversion of secreted progaline B into YPD7 into its active form occurs when the pH of the supernatant is lowered to pH 3.5 for 4.30 hours at 37 ° C. Thus, after incubation, the 30.7 kDa band is detected (fig. 9 B / line 3) due to the rupture of the PSI and loss of the propeptide (fig. 9 B / line 4: under non-reducing conditions HC and LC remain bound by disulfide bridges) (the loss of the propeptide is deduced by the lower molecular weight of the band corresponding to the recombinant enzyme and was verified by MALDI TOF in an assay not included in this document). The lowering of pH 30 activates progaline B which results in the supernatant showing proteolytic activity (122 ± 23 U) (fig. 9 C2).
    The enzymatic activities in YPD, YPD4 and YPD7 are not comparable due to the effect of pH on cell growth. The activation of progaline B when grown in YPD medium without buffering is due to the decrease in pH that occurs during the course of fermentation (fig. 6).
    This test demonstrates that the activation of recombinant progaline B is pH dependent and that by buffering the culture medium we can produce it in its inactive form and subsequently activate it by lowering the pH.

    Example 11. Activation pH of progaline B. 5
    The activation pH of progaline B cultured in pH7 buffered medium (YPD7) was determined by incubating the supernatants of a culture of the recombinant strain with a 0.2 M buffer volume at different pHs. The samples were incubated at 28 ° C for 30, 150 and 270 minutes, after which they were analyzed by Western Blot and their activity was measured by the method of Ageitos et al. 2006 (fig. 10 10 A and fig. B respectively). After 30 minutes of incubation in the pH 3.5-5.0 range, a band corresponding to the heavy chain of progaline B with the propeptide (37 kDa) was detected, while in the supernatants incubated at pH 6.6 and 7 only the band was observed 56 kDa corresponding to the unprocessed enzyme (fig. 10 A.1). When the incubation time was increased 15 (150 minutes), the propeptide breakage occurred, detecting the 30.7 kDa band corresponding to the heavy chain without the propeptide. The processing was complete when the supernatant was incubated at pH 3.5 (fig. 10 A.2, line 2); the conversion was slower when the supernatant was incubated at more alkaline pHs, thus the 30.7 kDa band was more tenuous at pH 4.6-5 and was not detected at pH 5.8, 6.6 and 7 (fig. 10 A.2) . 20 After 270 minutes, the activation of the supernatants in the range 4.3 - 5.8 results in a partial activation (the 37 kDa band is still visible), while at pH 6.6 and 7 progaline B is not activated (fig. 10, A.3).

    As can be seen in figure 10 B, samples in which progaline B has lost the propeptide show enzymatic activity on the k-casein (fig. 10 B) and this is greater depending on the loss of the propeptide.


     30



    权利要求:
    Claims (1)
    [1]
    1- A vector comprising a polynucleotide with the nucleotide sequence shown in SEQ ID NO: 1 or in SEQ ID NO: 2, or a variant thereof that has an identity degree of at least 80% with respect to to SEQ ID NO: 1 or to SEQ ID NO: 2 with aspartic protease activity of the 5 plant species Galium verum.
    2- A cell or microorganism comprising a vector according to claim 1.
     10
    3- A cell or microorganism that integrated into its genome comprises a polynucleotide with the nucleotide sequence shown in SEQ ID NO: 1 or in SEQ ID NO: 2, or a variant thereof that has a degree of identity of at minus 80% with respect to said SEQ ID NO: 1, with aspartic protease activity of the plant species Galium verum. fifteen
    4- A cell or microorganism according to claim 2 or 3 with the proviso that said cell is a yeast or a bacterium.
    5- A cell strain according to claim 4 with the proviso that said cell is the yeast Pichia pastoris deposited in the Spanish Collection of 20 Type Cultures (CECT) with the deposit number CECT 13141.
    6- Method of obtaining the coagulant comprising the production by fermentation of the aspartic proteases of Galium verum in a culture medium comprising:
    a) a host cell or microorganism according to claims 25 from 2 to 5,
    b) centrifugation of the culture medium and separation of the liquid part,
    c) filtration of the liquid part
    d) direct use of the same or concentration by ultrafiltration, chromatography, precipitation with ammonium sulfate or lyophilization of the liquid part.
    7- Method of obtaining the coagulant according to claim 6 wherein the culture medium is YPD.
    8- Procedure for obtaining the coagulant according to claim 6 and 7 wherein the centrifugation of the culture medium and the separation of the liquid part is carried out in a range of 1,500 to 20,000g. 5
    9- Method of obtaining the coagulant according to claim 6 to 8 wherein the culture temperature is between 20 and 35 ° C.
    10- Method of obtaining the coagulant according to claims 6 to 9 in which the recombinant aspartic protease of Galium verum is produced in its inactive form in a medium at alkaline pH and is subsequently activated 10 by lowering the pH.
    11- Method of obtaining the coagulant according to claim 10 with the proviso that the culture pH is between 7 and 14 and the activation pH is between 2 and 5.5
    12- A composition comprising the use of aspartic protease obtained from a host cell according to claims 2 to 5.
    13. Composition according to claim 12, further comprising an additive suitable for food.
    14. Preparation of a food product comprising the aspartic protease obtained by the method according to claims 6 to 11 or cells or microorganisms according to claims 2 to 5.
    15- Use of the aspartic protease obtained by means of a method according to claims 6 to 11 for milk coagulation.
    16- Use of the aspartic protease according to claim 15 which does not require prior activation for milk coagulation. 25
    17- Use of the aspartic protease obtained by means of a method according to claims 6 to 11 for cheese making.
    18- Use of the aspartic protease obtained by means of a method according to claims 6 to 11 for the accelerated ripening of the cheeses.
     30
    19- Use of the aspartic protease obtained by means of a method according to claims 6 to 11 for the production of dairy products enriched in bioactive peptides
     5


     10


     fifteen


     twenty


     25
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    同族专利:
    公开号 | 公开日
    WO2018115559A1|2018-06-28|
    ES2673702B2|2018-10-05|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    WO2000075283A1|1999-06-09|2000-12-14|Instituto De Ciencia Aplicada E Tecnologia |Production by yeasts of aspartic proteinases from plant origin with sheep's, cow's, goat's milk, etc. clotting and proteolytic activity|
    ES2336171A1|2007-07-27|2010-04-08|Universidad De Santiago De Compostela|Use of active recombinant chymosin|
    WO2014148931A2|2013-03-19|2014-09-25|Biocant - Associação De Transferência De Technologia|Aspartic proteases|
    CN109679940A|2019-01-23|2019-04-26|华南理工大学|Acid protease Candidapepsin and its heterogenous expression and purification process|
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    PCT/ES2017/070832| WO2018115559A1|2016-12-23|2017-12-20|Recombinant strain, method for producing aspartic proteases of galium verum and use in the dairy industry|
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