Patent Application
20230227804
The present invention relates to the field of genetic engineering. More specifically, the invention is directed towards obtaining improved production of a novel recombinant β-fructofuranosidase, encoded by fopA gene of Aspergillus niger as a secreted protein.
Fructose oligomers, also known as fructooligosaccharides (FOS) constitute a series of homologous oligosaccharides. Fructooligosaccharides are usually represented by the formula GFn and are mainly composed of 1-kestose (GF2), nystose (GF3) and β-fructofuranosylnystose (GF4), in which two, three, and four fructosyl units are bound at the β-2,1 position of glucose.
Fructooligosaccharides (FOS) are characterized by many beneficial properties such as low sweetness intensity and usefulness as a prebiotic. Due to the low sweetness intensity (about one-third to two-third as compared to sucrose) and low calorific values (approximately 0-3 kcal/g), fructooligosaccharides can be used in various kinds of food as a sugar substitute. Further, as a prebiotic, fructooligosaccharides have been reported for being used as protective agents against colon cancer, enhancing various parameters of the immune system, improving mineral adsorption, beneficial effects on serum lipid and cholesterol concentrations and exerting glycemic control for controlling obesity and diabetes (Dominguez, Ana Luisa, et al. “An overview of the recent developments on fructooligosaccharide production and applications.” Food and bioprocess technology 7.2 (2014): 324-337.)
However, fructooligosaccharides are found only in trace amounts as natural components in fruits, vegetables, and honey. Due to such low concentration, it is practically impossible to extract fructooligosaccharides from food.
Attempts have been made to produce fructooligosaccharides through enzymatic synthesis from sucrose by microbial enzymes with transfructosylation activity. However, the major constraints in the previous attempts have been the lower catalytic efficiency, feedback inhibition of the enzyme by glucose leading lower FOS yields and the requirement of longer time periods for conversion of sucrose by the enzymes expressed in the recombinant host system. Further, industrial production of microbial enzymes exhibiting transfructosylation activity is challenging due to additional limitations associated with large scale expression of enzyme, enzyme stability, fermentation and purification processes.
Commercial-scale production of fructooligosaccharides requires identification and mass production of efficient enzymes. Due to the aforesaid limitations, the production of microbial enzymes with efficient transfructosylation activity is a costly affair which in-turn increases the production cost of fructooligosaccharides.
Thus, there is a long-felt need for identifying and providing efficient, cheap and industrially scalable means for the production of microbial enzymes with superior transfructosylation activity, which in turn lowers the cost of production of fructooligosaccharides.
The technical problem to be solved in this invention is to identify and improve the yield of a novel β-fructofuranosidase (UniProtKB: Q96VC5_ASPNG) of Aspergillus niger.
The problem has been solved by overexpression of a novel β-fructofuranosidase of Aspergillus niger by engineering nucleic acid sequences, protein sequences, promoters, recombinant vectors, host cells and secretory signal peptides for achieving high yield of novel recombinant β-fructofuranosidase.
Additionally, the fermentation strategy has been modified to obtain a high yield of about 2-5 gm/L recombinant β-fructofuranosidase.
The present invention relates to nucleic acids, protein sequences, vectors and host cells for recombinant expression of a novel β-fructofuranosidase. The present invention also relates to precursor peptides containing signal peptides fused to a novel β-fructofuranosidase enzymes which enable generation of higher yield of the efficient enzyme as a secretory protein.
The invention also relates to a process for the expression of a novel recombinant β-fructofuranosidase as a secreted protein. The β-fructofuranosidase concentration is found to be about 2-5 gm/L. The enzyme exhibits almost 85% purity after filtration, which eliminates the need for costly chromatographic procedures.
The features of the present disclosure will become fully apparent from the following description taken in conjunction with the accompanying figures. With the understanding that the figures depict only several embodiments in accordance with the disclosure and are not to be considered limiting of its scope, the disclosure will be described further through the use of the accompanying figures.
SEQ ID NO: 1—Amino acid sequence of novel β-fructofuranosidase (654 amino acids)
SEQ ID NO: 2—Modified nucleic acid sequence of the gene encoding novel β-fructofuranosidase (1965 base pairs)
maxianus)
In all the secretory signal peptide sequences, a stretch of four amino acids (LEKR) was added for the efficient Kex2 processing of pre-protein.
SEQ ID NO: 23—Native nucleic acid sequence of the fopA gene (1965 base pairs) encoding secreted β-fructofuranosidase
Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which the methods belong. Although any vectors, host cells, methods and compositions similar or equivalent to those described herein can also be used in the practice or testing of the vectors, host cells, methods and compositions, representative illustrations are now described.
Where a range of values are provided, it is understood that each intervening value between the upper and lower limit of that range and any other stated or intervening value in that stated range, is encompassed within by the methods and compositions. The upper and lower limits of these smaller ranges may independently be included in the smaller ranges and are also encompassed within by the methods and compositions, subject to any specifically excluded limit in the stated range. Where the stated range includes one or both of the limits, ranges excluding either or both of those included limits are also included in the methods and compositions.
It is appreciated that certain features of the methods, which are, for clarity, described in the context of separate embodiments, may also be provided in combination in a single embodiment. Conversely, various features of the methods and compositions, which are, for brevity, described in the context of a single embodiment, may also be provided separately or in any suitable sub-combination. It is noted that, as used herein and in the appended claims, the singular forms “a”, “an”, and “the” include plural referents unless the context clearly dictates otherwise. It is further noted that the claims may be drafted to exclude any optional element. As such, this statement is intended to serve as antecedent basis for use of such exclusive terminology as “solely,” “only” and the like in connection with the recitation of claim elements or use of a “negative” limitation.
As will be apparent to those of skill in the art upon reading this disclosure, each of the individual embodiments described and illustrated herein has discrete components and features which may be readily separated from or combined with the features of any of the other embodiments without departing from the scope or spirit of the present methods. Any recited method can be carried out in the order of events recited or in any other order that is logically possible.
The term “host cell(s)” includes an individual cell or cell culture which can be, or has been, a recipient for the subject of expression constructs. Host cells include progeny of a single host cell. Host cells for the purposes of this invention refers to any strain of Pichia pastoris which can be suitably used for the purposes of the invention. Examples of strains that can be used for the purposes of this invention include wild type, mut+, mut S, mut− strains of Pichia such as KM71H, KM71, SMD1168H, SMD 1168, GS115, X33.
The term “recombinant strain” or “recombinant host cell(s)” refers to a host cell(s) which has been transfected or transformed with the expression constructs or vectors of this invention.
The term “expression vector” refers to any vector, plasmid or vehicle designed to enable the expression of an inserted nucleic acid sequence following transformation into the host.
The term “promoter” refers to DNA sequences that define where transcription of a gene begins. Promoter sequences are typically located directly upstream or at the 5′ end of the transcription initiation site. RNA polymerase and the necessary transcription factors bind to the promoter sequence and initiate transcription. Promoters can either be constitutive or inducible promoters. Constitutive promoters are the promoter which allows continual transcription of its associated genes as their expression is normally not conditioned by environmental and developmental factors. Constitutive promoters are very useful tools in genetic engineering because constitutive promoters drive gene expression under inducer-free conditions and often show better characteristics than commonly used inducible promoters. Inducible promoters are the promoters that are induced by the presence or absence of biotic or abiotic and chemical or physical factors. Inducible promoters are a very powerful tool in genetic engineering because the expression of genes operably linked to them can be turned on or off at certain stages of development or growth of an organism or in a particular tissue or cell type.
The term “operably linked” refers to the association of nucleic acid sequences on a single nucleic acid fragment so that the function of one is regulated by the other. For example, a promoter is operably linked with a coding sequence when it is capable of regulating the expression of that coding sequence (i.e., that the coding sequence is under the transcriptional control of the promoter).
The term “transcription” refers to the process of making an RNA copy of a gene sequence. This copy, called a messenger RNA (mRNA) molecule, leaves the cell nucleus and enters the cytoplasm, where it directs the synthesis of the protein, which it encodes.
The term “translation” refers to the process of translating the sequence of a messenger RNA (mRNA) molecule to a sequence of amino acids during protein synthesis. The genetic code describes the relationship between the sequence of base pairs in a gene and the corresponding amino acid sequence that it encodes. In the cell cytoplasm, the ribosome reads the sequence of the mRNA in groups of three bases to assemble the protein.
The term “expression” refers to the biological production of a product encoded by a coding sequence. In most cases, a DNA sequence, including the coding sequence, is transcribed to form a messenger-RNA (mRNA). The messenger-RNA is then translated to form a polypeptide product that has a relevant biological activity. Also, the process of expression may involve further processing steps to the RNA product of transcription, such as splicing to remove introns, and/or post-translational processing of a polypeptide product.
The term “modified nucleic acid” as used herein is used to refer to a nucleic acid encoding β-fructofuranosidase fused to a signal peptide. In embodiments, the modified nucleic acid is represented by SEQ ID NO:13, SEQ ID NO:14, SEQ ID NO:15, SEQ ID NO:16, SEQ ID NO:17, SEQ ID NO:18, SEQ ID NO:19, SEQ ID NO:20, SEQ ID NO: 21, SEQ ID NO: 22 or a functionally equivalent variant thereof. The functional variant includes any nucleic acid having substantial or significant sequence identity or similarity to SEQ ID NO:13-22, and which retains the biological activities of the same.
The terms “polypeptide”, “peptide” and “protein” are used interchangeably herein to refer to two or more amino acid residues joined to each other by peptide bonds or modified peptide bonds. The terms apply to amino acid polymers in which one or more amino acid residue is an artificial chemical mimetic of a corresponding naturally occurring amino acid, as well as to naturally occurring amino acid polymers, those containing modified residues, and non-naturally occurring amino acid polymer. “Polypeptide” refers to both short chains, commonly referred to as peptides, oligopeptides or oligomers, and to longer chains, generally referred to as proteins. Polypeptides may contain amino acids other than the 20 gene-encoded amino acids. Likewise, “protein” refers to at least two covalently attached amino acids, which includes proteins, polypeptides, oligopeptides, and peptides. A protein may be made up of naturally occurring amino acids and peptide bonds, or synthetic peptidomimetic structures. Thus “amino acid”, or “peptide residue”, as used herein means both naturally occurring and synthetic amino acids. “Amino acid” includes imino acid residues such as proline and hydroxyproline. The side chains may be in either the (R) or the (S) configuration.
The term “signal peptide” or “signal peptide sequence” is defined herein as a peptide sequence usually present at the N-terminal end of newly synthesized secretory or membrane polypeptides which directs the polypeptide across or into a cell membrane of the cell (the plasma membrane in prokaryotes and the endoplasmic reticulum membrane in eukaryotes). It is usually subsequently removed. In particular said signal peptide may be capable of directing the polypeptide into a cell's secretory pathway.
The term “precursor peptide” as used herein refers to a peptide comprising a signal peptide (also known as leader sequences) operably linked to the β-fructofuranosidase of Aspergillus niger. The signal peptides are cleaved off during post-translational modifications inside the Pichia host cells and the mature β-fructofuranosidase (SEQ ID NO: 1) is released into the medium.
The term “variant” as used herein in reference to pre-cursor peptides/proteins refers to peptides with amino acid substitutions, additions, deletions or alterations that do not substantially decrease the activity of the signal peptide or the enzyme. Variants include a structural as well as functional variants. The term variant also includes the use of a substituted amino acid in place of an unsubstituted parent amino acid.
Amino acid substitution tables providing functionally similar amino acids are well known to one of ordinary skill in the art. The following six groups are examples of amino acids that are considered to be variants for one another:
The present invention discloses nucleic acids, vectors and recombinant host cells for efficient production of biologically active and soluble recombinant β-fructofuranosidase of Aspergillus niger as a secreted protein. Further, the invention provides a process for commercial-scale production of recombinant β-fructofuranosidase.
The invention contemplates a multidimensional approach for achieving a high yield of novel recombinant β-fructofuranosidase in a heterologous host. The native gene for β-fructofuranosidase has been modified for expression in Pichia pastoris. Further, the modified gene has been fused to one or more signal peptides.
In one embodiment, the modified nucleic acid encoding novel 1-fructofuranosidase of Aspergillus niger is represented by SEQ ID NO: 2.
In another embodiment, the modified nucleic acid is fused to one or more signal peptide.
In another embodiment, the signal peptide is selected from Alpha-factor of S. cerevisiae (FAK), Alpha-factor full of S. cerevisiae (FAKS) of S. cerevisiae, Alpha factor_T of S. cerevisiae (AT), Alpha-amylase of Aspergillus niger (AA), Glucoamylase of Aspergillus awamori (GA), Inulinase of Kluyveromyces maxianus (IN), Invertase of S. cerevisiae (IV), Killer protein of S. cerevisiae (KP), Lysozyme of Gallus gallus (LZ), Serum albumin ofHomo sapiens (SA)
In another embodiment, the signal peptide are provided in the below Table 5.
maxianus)
In another embodiment, the signal peptide is selected from a list of modified signal peptides as described in Table 1.
In another embodiment, the nucleic acid fused to one or more modified signal peptide selected from a group comprising SEQ ID NO: 13, SEQ ID NO: 14, SEQ ID NO: 15, SEQ ID NO: 16, SEQ ID NO: 17, SEQ ID NO: 18, SEQ ID NO: 19, SEQ ID NO: 20, SEQ ID NO: 21, SEQ ID NO: 22 and variants thereof.
In another embodiment, the modified nucleic acid is cloned in an expression vector.
In another embodiment, the expression vector is configured for secretory or intracellular expression of recombinant β-fructofuranosidase from Aspergillus niger.
In yet another embodiment, the expression vector is selected from a group comprising pPICZαA, pPICZαB, pPICZαC, pGAPZαA, pGAPZαB, pGAPZαC, pPIC3, pPIC3.5, pPIC3.5K, PAO815, pPIC9, pPIC9K, IL-D2 and pHIL-S1.
The expression of the modified β-fructofuranosidase (fopA) gene fused to a signal peptide is preferably driven by a constitutive or inducible promoter.
In another embodiment, the nucleic acid to be expressed in operably linked to the promoter.
In another embodiment, the constitutive or inducible promoter is selected from a group listed in Table 6.
In another embodiment, the promoter is an AOX1 promoter, which is induced by methanol and repressed by glucose.
In an embodiment, the expression vector containing the modified gene of interest (β-fructofuranosidase gene fused to a nucleic acid encoding signal peptide) is transformed in an appropriate host.
In another embodiment, the expression vector containing the gene of interest is transformed in yeast cells.
In another embodiment, the yeast cell is a Pichia pastoris.
In yet another embodiment, the Pichia Pastoris host cell is a mut+, mut S or mut-strains. Mut+ represents methanol utilization plus phenotype.
In yet another embodiment, the Pichia Pastoris host cell strain is selected from a group comprising KM71H, KM71, SMD 1168H, SMD 1168, GS 115, X33.
In another embodiment, the invention provides β-fructofuranosidase pre-cursor peptides, wherein β-fructofuranosidase of Aspergillus niger is fused to one or more signal peptide.
In another embodiment, β-fructofuranosidase of Aspergillus niger has the amino acid sequence set forth in SEQ ID NO:1 and functional variants thereof. Functional variant includes any protein sequence having substantial or significant sequence identity or similarity to SEQ ID NO:1 and or having a substantial or significant structural identity or similarity to SEQ ID NO:1, and which retains the biological activities of the same.
In another embodiment, the signal peptide is selected from a group comprising Alpha-factor full of S. cerevisiae (FAK) set forth in SEQ ID NO: 3, Alpha-factor full of S. cerevisiae (FAKS) set forth in SEQ ID NO: 4, Alpha factor_T of S. cerevisiae (AT) set forth in SEQ ID NO: 5, Alpha-amylase of Aspergillus niger (AA) set forth in SEQ ID NO: 6, Glucoamylase of Aspergillus awamori (GA) set forth in SEQ ID NO: 7, Inulinase of Kluyveromyces maxianus (IN) set forth in SEQ ID NO: 8, Invertase of S. cerevisiae (IV) set forth in SEQ ID NO: 9, Killer protein of S. cerevisiae (KP) set forth in SEQ ID NO: 10, Lysozyme of Gallus gallus (LZ) set forth in SEQ ID NO: 11, Serum albumin of Homo sapiens (SA) set forth in SEQ ID NO: 12, and variants thereof.
In an embodiment, the process for the production of recombinant β-fructofuranosidase of Aspergillus niger is provided.
Aspects of the present invention relate to fermentation of recombinant Pichia pastoris cells containing modified recombinant β-fructofuranosidase (fopA) gene. After completion of the fermentation, the fermentation broth is subjected to centrifugation and filtered using microfiltration and the recombinant enzyme is separated. The recovered recombinant enzyme is concentrated using Tangential Flow Ultra-filtration or evaporation and finally the concentrated enzyme is formulated.
In one embodiment, the process for expressing β-fructofuranosidase of Aspergillus niger at high levels comprises the steps of:
In another embodiment, the fermentation medium is basal salt medium as described in Table 7.
In yet another embodiment, the supernatant from the fermentation broth is harvested using centrifugation.
In one embodiment, the percentage of inoculum or starter culture to initiate the fermenter culture is in the range of 2.0% to 15.0% (v/v).
In another embodiment, the pH of the fermentation medium is maintained in the range of 4.0 to 7.5 as the secreted enzyme undergoes proper folding and is biologically active at this pH range.
In yet another embodiment, the temperature of the fermentation process is in the range of 15° C. to 40° C.
In another embodiment, the time for fermentation process is in the range of 50-150 hrs.
In a further, embodiment, the fermentation broth is centrifuged at a speed in the range from 2000×g to 15000×g using continuous online centrifugation.
The supernatant obtained after centrifugation is subjected to microfiltration and purified to recover biologically active recombinant β-fructofuranosidase.
In one embodiment, the supernatant obtained after centrifugation is concentrated using a Tangential Flow Filtration based Ultra filtration System.
The cut-off size of the membranes used in Tangential Flow Filtration (TFF) systems that may be used to remove impurities and to concentrate the collected culture supernatant may range between 5 to 100 kDa.
In another embodiment, no centrifugation is required for the process due to the high yield and purity of the secreted enzyme.
The β-fructofuranosidase concentration obtained in this invention is found to be in the range of 2-5 gm/L and the purity is about 85%.
The following examples particularly describe the manner in which the invention is to be performed. But the embodiments disclosed herein do not limit the scope of the invention in any manner.
The cDNA of the native β-fructofuranosidase (fopA) of Aspergillus niger is represented by SEQ ID NO: 23 and the amino acid sequence of novel β-fructofuranosidase is represented by SEQ ID NO: 1.
The native cDNA was modified for maximizing expression in Pichia pastoris. The modified nucleic acid is represented by SEQ ID NO: 2. The differences between the native and the modified sequence is depicted in
An expression cassette encoding the β-fructofuranosidase was modified for maximizing expression in Pichia pastoris. The modified open reading frame contains the modified nucleotide sequence (SEQ ID NO: 2) encoding β-fructofuranosidase fused to a signal peptide. The nucleic acids have been designed such that the encoded signal peptides contain an additional stretch of four amino acids (LEKR) for the efficient Kex2 processing of precursor peptide.
The preferred codons for expression in Pichia pastoris have been used in place of rare codons.
The nucleotide sequence of the modified open reading frames encoding for β-fructofuranosidase fused with modified signal peptides are given below:
The SEQ ID NO: 13 nucleic acid sequence was chemically synthesized cloned into pPICZαA vector and remaining modified nucleic acid sequences have been generated by overlap extension PCR using SEQ ID NO: 13 expression cassette as a template.
Recombinant pre-cursor proteins were obtained by translating the gene encoding for β-fructofuranosidase of Aspergillus niger fused with signal peptides.
The signal peptides used in the modified precursor peptides were Alpha-factor of S. cerevisiae (FAK) represented by SEQ ID NO: 3, Alpha-factor full of S. cerevisiae (FAKS) represented by SEQ ID NO: 4, Alpha-factor_T of S. cerevisiae (AT) represented by SEQ ID NO: 5, Alpha-amylase of Aspergillus niger (AA) represented by SEQ ID NO: 6, Glucoamylase of Aspergillus awamori (GA) represented by SEQ ID NO: 7, Inulinase of Kluyveromyces maxianus (IN) represented by SEQ ID NO: 8, Invertase of S. cerevisiae (IV) represented by SEQ ID NO: 9, Killer protein of S. cerevisiae (KP) represented by SEQ ID NO: 10, Lysozyme of Gallus gallus (LZ) represented by SEQ ID NO: 11 and Serum albumin of Homo sapiens (SA) represented by SEQ ID NO: 12. The modified signal peptides contain an additional stretch of four amino acids (LEKR) for the efficient Kex2 processing of precursor peptide.
The signal peptides are cleaved off during post-translational modifications inside the Pichia host cells and the mature recombinant β-fructofuranosidase comprising the amino acid sequence of SEQ ID NO: 1 is released into the medium.
The vector used in the process was pPICZαA. The vectors contained the modified open reading frames as described in Example 1 and an inducible promoter, AOX). The modified sequence encoding for the recombinant protein was cloned into the pPICZαA vector.
The modified nucleic acid SEQ ID NO: 2 encoding f-fructofuranosidase (fopA) gene was cloned between XhoI/SacII restriction sites present in the MCS of pPICZαA vector to bring signal sequence Alpha-factor of S. cerevisiae (FAK) in frame to create SEQ ID NO: 13 expression cassette using regular molecular biology procedures. The vector map for pPICZαA is represented in
The putative recombinant plasmids were selected on low salt-LB media containing 25 μg/ml Zeocin and screened by XhoI/SacII restriction digestion analysis.
The recombinant plasmid pPICZαA-fopA was confirmed by XhoI/SacII restriction digestion analysis which resulted in release of 1980 bp fragment. The results of the restriction digestion analysis are depicted in
Thereafter, Pichia pastoris KM71H cells were electroporated with linearized recombinant pPICZαA-fopA DNA. The Pichia integrants were selected on yeast extract peptone dextrose sorbitol agar (YPDSA) containing 100 μg/ml Zeocin.
The integration was screened with colony PCR (cPCR). For cPCR, a template from each of the Pichia integrants was generated by the alkali lysis method. The results of the colony PCR screening are depicted in
The Pichia integrants were grown for 48 h in BMD1 media and further induced first with BMM2 and then successively with BMM10 media which provided final concentration of 0.5% methanol in the culture medium. At the end of 96 hrs induction period, culture supernatants from different clones were harvested. Total protein from each of the harvested supernatants was precipitated with 20% TCA and analyzed on SDS-PAGE.
Upon induction β-fructofuranosidase protein bands were seen at the size of approximately 110 kDa as depicted in
The calculated molecular weight was about 70.85 kDa. The increase in molecular weight may have been contributed by glycosylation.
Fermentation of recombinant Pichia pastoris cells containing the modified β-fructofuranosidase (fopA) gene as described in Example 1 was carried out in a 50 L fermenter. Fermentation was carried out in basal salt medium as described herein. The recombinant host selected was KM71H, which is a mut S strain that metabolizes methanol in a slow manner.
The pre-seed was generated by inoculating from the glycerol stock in 25 mL of sterile YEPG medium and growing at 30° C. in a temperature-controlled orbital shaker overnight. For generating seed, the inoculum was grown in Basal salt medium in baffled shake flasks at 30° C. in a temperature-controlled orbital shaker till OD600 of 15-25 was reached.
The entire process of fermentation from the inoculation of fermenter with seed culture to final harvesting took about 130 hrs. Basal salt medium was prepared and sterilized in situ in the fermenter.
The composition of basal salt medium optimized for the fermentation process is provided in Table 7.
Pichia Trace Minerals (PTM) salt solution was prepared as described in Table 8. PTM salts were dissolved and made up to 1 L volume and filter sterilized. PTM salt solution was included at the rate of 4 ml per liter of initial media volume after sterilization of the basal salt media
The growth phase starts by inoculating basal salt medium in 50 L fermenter with 5% seed culture and continues for about 24 hours. The dissolved oxygen (DO) levels were continuously monitored and never allowed to drop below 40%.
After 18 h, a DO spike was observed indicating the depletion of carbon source (Glycerol). A glycerol fed-batch was initiated by feeding 50% Glycerol (with 12 ml of PTM salts per liter of feed) for about six hours till the OD600 reached 200.
Once sufficient biomass was generated, the induction phase was initiated by discontinuing glycerol feed and starting methanol feed. Methanol (supplemented with 12 ml of PTM salts per liter of feed) was fed at the rate of 0.5 g to 3 g per liter of initial fermentation volume. The DO was maintained at 40% and methanol feed was accordingly adjusted.
The induction of β-fructofuranosidase (fopA) gene was monitored periodically by analyzing culture supernatant by enzyme activity assay. The induction phase was continued for about 100 hours till the OD600 reached 600 and wet biomass reached ˜560 grams per liter of culture broth.
The fermentation was stopped after 130 hours and enzyme activity in the fermenter broth at the end of fermentation was determined to be 10573 units by DNS method (Miller, 1959). One unit is defined as the amount of enzyme required to release one micromole of reducing sugars (glucose equivalents) from 10% sucrose solution in 100 mM citrate buffer pH 5.5 at 55° C. The total amount of recombinant β-fructofuranosidase in the culture broth was estimated by Bradford assay.
The fermentation parameters considered were as given in Table 9. These essential parameters were monitored during the fermentation process.
Harvesting of the enzyme is performed by continuous centrifugation at 8000 RPM. Clear supernatant obtained after centrifugation was subjected to microfiltration using 0.1 microns cut off spiral wound TFF membrane. The filtrate is further subjected to ultrafiltration and diafiltration using 10 kDa cutoff spiral wound TFF membrane and sufficiently concentrated and to reach the desired activity. The enzyme was formulated by including 35-50% of glycerol and food-grade preservatives in the final preparation. The final purity of the enzyme was observed to be 85% as determined by SDS-PAGE analysis.
The β-fructofuranosidase concentration was found to be about 2.4 gm/L. In most of the batches, the concentration was 2-5 gm/L. The purity of the recombinant β-fructofuranosidase was observed to be about 85%.
Studies were conducted to estimate the activity of β-fructofuranosidase. For the estimation studies, the amount of reducing sugar generated due to the action of β-fructofuranosidase enzyme was calculated using DNS (3,5 Dinitrosalicylic acid) method (G. L. Miller, “Use of dinitrosalicylic acid reagent for determination of reducing sugar”, Anal. Chem., 1959, 31, 426-428).
For conducting the enzyme activity assay, 10% Sucrose (dissolved in 100 mM Citrate buffer) was used as the substrate. β-fructofuranosidase was recovered from the fermentation broth and processed through ultra-filtration. The ultra-filtered sample then diluted 25,000× by serial dilution in 100 mM Citrate buffer and was used. The reaction volume was 2.5 mL. The pH was maintained at 5.5 and the reaction was continued for 15 minutes.
After incubation 3 mL of DNS (3,5 Dinitrosalicylic acid) was added to each reaction mixture and boiled for 10 min, cooled and read absorbance at 540 nm, spectrophotometrically.
The OD of glucose at different concentration was measured as shown in Table 10 and depicted in
Studies were conducted to understand the ability of the enzyme in the formation of fructooligosaccharides. A 100 ml, solution of 90% (w/v) Sucrose was prepared in 150 mM sodium citrate buffer pH 5.5. To this, 96.7 μL of β-fructofuranosidase enzyme having 51692 Unit/ml of activity (equivalent to total of 5000 Units of enzyme), was added.
The reaction was set up in a 250 ml, conical flask and incubated at 65° C. and 220 rpm. At regular time intervals, samples were taken and analyzed on Thin Layer Chromatographic (TLC) plates.
Glucose, sucrose, fructose and FOS (containing kestose, nystose and fructofuranosylnystose) were used as standards for the thin layer chromatographic analysis. The mobile phase used was n-Butanol:Glacial acetic acid:Water (4:2:2 v/v) and the developing/staining solution used was urea phosphoric acid.
The sample was further subjected to High Performance Liquid Chromatography (HPLC) for quantitative estimation of the production of fructooligosaccharides. The HPLC analysis was done using an amine column (Zorbax NH2 column, Agilent Technologies) having 4.6 (ID)×150 mm (length) and 5 μm (particle size). The standard solutions of glucose, fructose, kestose, nystose, fructofuranosylnystose and sucrose of different concentrations were run for generating standard curves.
100 ml of 90% (w/v) sucrose solution was reacted with β-fructofuranosidase enzyme for the conversion of sucrose into FOS. The quantities of recovered FOS, sucrose, glucose, and fructose from the reaction after terminating the reaction by heat at the end of 60 min were measured and presented as 90% and 100% sucrose basis.
The studies demonstrated that the purified enzymes are able to effectively convert a very high amount of sugars into fructooligosaccharides.
The harvested β-fructofuranosidase of Aspergillus niger was characterized to identify bioactive fragments. It was found that following bioactive fragments of β-fructofuranosidase are conserved and accounts for the catalytic activities:
It was further found that the following amino acids residues in β-fructofuranosidase of Aspergillus niger were involved in forming a hydrogen bond network around the catalytic triad. The hydrogen bond network is important for the stable stereochemistry around the catalytic triad:
| Number | Date | Country | Kind |
|---|---|---|---|
| 201941048686 | Nov 2019 | IN | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/IN2020/050985 | 11/27/2020 | WO |
