Patent Grant
10093914
The present invention relates to the use of nucleic acid sequences encoding xylose isomerases in the transformation of a eukaryotic microbial host cell to confer to the host cell the ability of isomerising xylose to xylulose. The transformed host cell is used in a process for the production of ethanol and other fermentation products by fermentation of a pentose-containing medium.
Economically viable ethanol production from the hemicellulose fraction of plant biomass requires the simultaneous conversion of both pentoses and hexoses at comparable rates and with high yields. Yeasts, in particular Saccharomyces spp., are the most appropriate candidates for this process since they can grow fast on hexoses, both aerobically and anaerobically. Furthermore, they are much more resistant to the toxic environment of lignocellulose hydrolysates than (genetically modified) bacteria.
Although wild-type S. cerevisiae strains can slowly metabolise the pentose sugar xylulose, they are not capable of metabolising xylose. Already in the 1980's it was suggested that metabolic engineering of yeasts for xylose utilization should be based on the introduction of xylose isomerase (XI, EC 5.3.1.5) rather than expressing heterologous xylose reductase and xylitol dehydrogenase to convert xylose into xylulose. Unfortunately, all attempts of introducing a bacterial xylose isomerase in S. cerevisiae have failed to produce a functionally expressed xylose isomerase with the notable exception of the T. thermophilus isomerase. This enzyme was functionally expressed in S. cerevisiae but only very low activities were observed at growth permitting temperatures. This situation drastically changed when a newly discovered xylose isomerase from the anaerobic fungus Piromyces Sp.E2 was introduced in S. cerevisiae and high levels of enzyme activities were observed enabling this strain to grow anaerobically and produce ethanol from xylose (WO 03/062430 and WO 06/009434). Such yeast strains for the first time provided specific rates of xylose consumption and ethanol formation that are compatible with ethanol production at a commercial scale.
Since the discovery of the functional expression of the Piromyces xylose isomerase in yeast several reports have appeared of functional expression in yeasts of other xylose isomerases, all of which share more than 70% amino acid sequence identity with the Piromyces enzyme, such e.g. the bacterial xylose isomerase from Bacteroides (WO 04/099381; WO 06/009434; WO 09/109633), and the fungal xylose isomerases from Cyllamyces (WO 04/099381) and Orpinomyces (Madhavan et al., 2008, DOI 10.1007/s00253-008-1794-6).
However, prior to Dec. 24, 2008 no reports have issued of functional expression in yeasts of xylose isomerases having less than 70% amino acid sequence identity with the Piromyces enzyme. More recently, in February 2009, Brat et al. (2009, Appl. Environ. Microbiol. 75: 2304-2311) published functional expression in the yeast S. cerevisiae of a xylose isomerise from the anaerobic bacterium Clostridium phytofermentans, the amino acid sequence of which shares only 52% identity with that of the Piromyces enzyme.
To date some 450 xylose isomerase amino acid sequences are publicly available in Genbank and other sequence databases, including the xylose isomerase sequences of Piromyces, Cyllamyces aberensis, Physcomitrella patens, Arabidopsis thaliana, Haemophilus somnus, Ciona intestinalis, Clostridium difficile, Thermatoga maritime, Bacteroides fragilis, Burkholderia phytofirmans, Arthrobacter aurescens and Fusobacterium mortiferum.
There is, however, still a need in the art for nucleotide sequences encoding other xylose isomerases that may be used to transform host cells like S. cerevisiae to confer to them the ability of isomerising xylose to xylulose, so as to enable the use of thus transformed host cell in processes for the production of ethanol or other fermentation products by fermentation of pentose-containing feedstock.
The enzyme “xylose isomerase” (EC 5.3.1.5) is herein defined as an enzyme that catalyses the direct isomerisation of D-xylose into D-xylulose and vice versa. The enzyme is also known as a D-xylose ketoisomerase. Some xylose isomerases are also capable of catalysing the conversion between D-glucose and D-fructose and are therefore sometimes referred to as glucose isomerase. Xylose isomerases require magnesium as cofactor. Xylose isomerases of the invention may be further defined by their amino acid sequence as herein described below. Likewise xylose isomerases may be defined by the nucleotide sequences encoding the enzyme as well as by nucleotide sequences hybridising to a reference nucleotide sequence encoding a xylose isomerase as herein described below. A unit (U) of xylose isomerase activity is herein defined as the amount of enzyme producing 1 nmol of xylulose per minute, in a reaction mixture containing 50 mM phosphate buffer (pH 7.0), 10 mM xylose and 10 mM MgCl2, at 37° C. Xylulose formed was determined by the method of Dische and Borenfreund (1951, J. Biol. Chem. 192: 583-587) or by HPLC as described in the Examples.
Sequence identity is herein defined as a relationship between two or more amino acid (polypeptide or protein) sequences or two or more nucleic acid (polynucleotide) sequences, as determined by comparing the sequences. In the art, “identity” also means the degree of sequence relatedness between amino acid or nucleic acid sequences, as the case may be, as determined by the match between strings of such sequences. “Similarity” between two amino acid sequences is determined by comparing the amino acid sequence and its conserved amino acid substitutes of one polypeptide to the sequence of a second polypeptide. “Identity” and “similarity” can be readily calculated by known methods. The terms “sequence identity” or “sequence similarity” means that two (poly)peptide or two nucleotide sequences, when optimally aligned, preferably over the entire length (of at least the shortest sequence in the comparison) and maximizing the number of matches and minimizes the number of gaps such as by the programs ClustalW (1.83), GAP or BESTFIT using default parameters, share at least a certain percentage of sequence identity as defined elsewhere herein. GAP uses the Needleman and Wunsch global alignment algorithm to align two sequences over their entire length, maximizing the number of matches and minimizes the number of gaps. Generally, the GAP default parameters are used, with a gap creation penalty=50 (nucleotides)/8 (proteins) and gap extension penalty=3 (nucleotides)/2 (proteins). For nucleotides the default scoring matrix used is nwsgapdna and for proteins the default scoring matrix is Blosum62 (Henikoff & Henikoff, 1992, PNAS 89, 915-919). A preferred multiple alignment program for aligning protein sequences of the invention is ClustalW (1.83) using a blosum matrix and default settings (Gap opening penalty: 10; Gap extension penalty: 0.05). It is clear than when RNA sequences are said to be essentially similar or have a certain degree of sequence identity with DNA sequences, thymine (T) in the DNA sequence is considered equal to uracil (U) in the RNA sequence. Sequence alignments and scores for percentage sequence identity may be determined using computer programs, such as the GCG Wisconsin Package, Version 10.3, available from Accelrys Inc., 9685 Scranton Road, San Diego, Calif. 92121-3752 USA or the open-source software Emboss for Windows (current version 2.7.1-07). Alternatively percent similarity or identity may be determined by searching against databases such as FASTA, BLAST, etc.
Preferred methods to determine identity are designed to give the largest match between the sequences tested. Methods to determine identity and similarity are codified in publicly available computer programs. Preferred computer program methods to determine identity and similarity between two sequences include e.g. the GCG program package (Devereux, J., et al., Nucleic Acids Research 12 (1):387 (1984)), BestFit, BLASTP, BLASTN, and FASTA (Altschul, S. F. et al., J. Mol. Biol. 215:403-410 (1990). The BLAST X program is publicly available from NCBI and other sources (BLAST Manual, Altschul, S., et al., NCBI NLM NIH Bethesda, Md. 20894; Altschul, S., et al., J. Mol. Biol. 215:403-410 (1990). The well-known Smith Waterman algorithm may also be used to determine identity.
Preferred parameters for polypeptide sequence comparison include the following: Algorithm: Needleman and Wunsch, J. Mol. Biol. 48:443-453 (1970); Comparison matrix: BLOSSUM62 from Hentikoff and Hentikoff, Proc. Natl. Acad. Sci. USA. 89:10915-10919 (1992); Gap Penalty: 12; and Gap Length Penalty: 4. A program useful with these parameters is publicly available as the “Ogap” program from Genetics Computer Group, located in Madison, Wis. The aforementioned parameters are the default parameters for amino acid comparisons (along with no penalty for end gaps).
Preferred parameters for nucleic acid comparison include the following: Algorithm: Needleman and Wunsch, J. Mol. Biol. 48:443-453 (1970); Comparison matrix: matches=+10, mismatch=0; Gap Penalty: 50; Gap Length Penalty: 3. Available as the Gap program from Genetics Computer Group, located in Madison, Wis. Given above are the default parameters for nucleic acid comparisons.
Optionally, in determining the degree of amino acid similarity, the skilled person may also take into account so-called “conservative” amino acid substitutions, as will be clear to the skilled person. Conservative amino acid substitutions refer to the interchangeability of residues having similar side chains. For example, a group of amino acids having aliphatic side chains is glycine, alanine, valine, leucine, and isoleucine; a group of amino acids having aliphatic-hydroxyl side chains is serine and threonine; a group of amino acids having amide-containing side chains is asparagine and glutamine; a group of amino acids having aromatic side chains is phenylalanine, tyrosine, and tryptophan; a group of amino acids having basic side chains is lysine, arginine, and histidine; and a group of amino acids having sulphur-containing side chains is cysteine and methionine. Preferred conservative amino acids substitution groups are: valine-leucine-isoleucine, phenylalanine-tyrosine, lysine-arginine, alanine-valine, and asparagine-glutamine. Substitutional variants of the amino acid sequence disclosed herein are those in which at least one residue in the disclosed sequences has been removed and a different residue inserted in its place. Preferably, the amino acid change is conservative. Preferred conservative substitutions for each of the naturally occurring amino acids are as follows: Ala to ser; Arg to lys; Asn to gln or his; Asp to glu; Cys to ser or ala; Gln to asn; Glu to asp; Gly to pro; His to asn or gln; Ile to leu or val; Leu to ile or val; Lys to arg; gln or glu; Met to leu or ile; Phe to met, leu or tyr; Ser to thr; Thr to ser; Trp to tyr; Tyr to tip or phe; and, Val to ile or leu.
Nucleotide sequences encoding xylose isomerases of the invention may also be defined by their capability to hybridise with the nucleotide sequences of SEQ ID NO. 2, respectively, under moderate, or preferably under stringent hybridisation conditions. Stringent hybridisation conditions are herein defined as conditions that allow a nucleic acid sequence of at least about 25, preferably about 50 nucleotides, 75 or 100 and most preferably of about 200 or more nucleotides, to hybridise at a temperature of about 65° C. in a solution comprising about 1 M salt, preferably 6×SSC or any other solution having a comparable ionic strength, and washing at 65° C. in a solution comprising about 0.1 M salt, or less, preferably 0.2×SSC or any other solution having a comparable ionic strength. Preferably, the hybridisation is performed overnight, i.e. at least for 10 hours and preferably washing is performed for at least one hour with at least two changes of the washing solution. These conditions will usually allow the specific hybridisation of sequences having about 90% or more sequence identity.
Moderate conditions are herein defined as conditions that allow a nucleic acid sequences of at least 50 nucleotides, preferably of about 200 or more nucleotides, to hybridise at a temperature of about 45° C. in a solution comprising about 1 M salt, preferably 6×SSC or any other solution having a comparable ionic strength, and washing at room temperature in a solution comprising about 1 M salt, preferably 6×SSC or any other solution having a comparable ionic strength. Preferably, the hybridisation is performed overnight, i.e. at least for 10 hours, and preferably washing is performed for at least one hour with at least two changes of the washing solution. These conditions will usually allow the specific hybridisation of sequences having up to 50% sequence identity. The person skilled in the art will be able to modify these hybridisation conditions in order to specifically identify sequences varying in identity between 50% and 90%.
A “nucleic acid construct” or “nucleic acid vector” is herein understood to mean a man-made nucleic acid molecule resulting from the use of recombinant DNA technology. The term “nucleic acid construct” therefore does not include naturally occurring nucleic acid molecules although a nucleic acid construct may comprise (parts of) naturally occurring nucleic acid molecules. The terms “expression vector” or expression construct” refer to nucleotide sequences that are capable of affecting expression of a gene in host cells or host organisms compatible with such sequences. These expression vectors typically include at least suitable transcription regulatory sequences and optionally, 3′ transcription termination signals. Additional factors necessary or helpful in effecting expression may also be present, such as expression enhancer elements. The expression vector will be introduced into a suitable host cell and be able to effect expression of the coding sequence in an in vitro cell culture of the host cell. The expression vector will be suitable for replication in the host cell or organism of the invention.
As used herein, the term “promoter” or “transcription regulatory sequence” refers to a nucleic acid fragment that functions to control the transcription of one or more coding sequences, and is located upstream with respect to the direction of transcription of the transcription initiation site of the coding sequence, and is structurally identified by the presence of a binding site for DNA-dependent RNA polymerase, transcription initiation sites and any other DNA sequences, including, but not limited to transcription factor binding sites, repressor and activator protein binding sites, and any other sequences of nucleotides known to one of skill in the art to act directly or indirectly to regulate the amount of transcription from the promoter. A “constitutive” promoter is a promoter that is active in most tissues under most physiological and developmental conditions. An “inducible” promoter is a promoter that is physiologically or developmentally regulated, e.g. by the application of a chemical inducer.
The term “selectable marker” is a term familiar to one of ordinary skill in the art and is used herein to describe any genetic entity which, when expressed, can be used to select for a cell or cells containing the selectable marker. The term “reporter” may be used interchangeably with marker, although it is mainly used to refer to visible markers, such as green fluorescent protein (GFP). Selectable markers may be dominant or recessive or bidirectional.
As used herein, the term “operably linked” refers to a linkage of polynucleotide elements in a functional relationship. A nucleic acid is “operably linked” when it is placed into a functional relationship with another nucleic acid sequence. For instance, a transcription regulatory sequence is operably linked to a coding sequence if it affects the transcription of the coding sequence. Operably linked means that the DNA sequences being linked are typically contiguous and, where necessary to join two protein encoding regions, contiguous and in reading frame.
The terms “protein” or “polypeptide” are used interchangeably and refer to molecules consisting of a chain of amino acids, without reference to a specific mode of action, size, 3-dimensional structure or origin.
“Fungi” (singular fungus) are herein understood as heterotrophic eukaryotic microorganism that digest their food externally, absorbing nutrient molecules into their cells. Fungi are a separate kingdom of eukaryotic organisms and include yeasts, molds, and mushrooms. The terms fungi, fungus and fungal as used herein thus expressly includes yeasts as well as filamentous fungi.
The term “gene” means a DNA fragment comprising a region (transcribed region), which is transcribed into an RNA molecule (e.g. an mRNA) in a cell, operably linked to suitable regulatory regions (e.g. a promoter). A gene will usually comprise several operably linked fragments, such as a promoter, a 5′ leader sequence, a coding region and a 3′nontranslated sequence (3′end) comprising a polyadenylation site. “Expression of a gene” refers to the process wherein a DNA region which is operably linked to appropriate regulatory regions, particularly a promoter, is transcribed into an RNA, which is biologically active, i.e. which is capable of being translated into a biologically active protein or peptide.
The term “homologous” when used to indicate the relation between a given (recombinant) nucleic acid or polypeptide molecule and a given host organism or host cell, is understood to mean that in nature the nucleic acid or polypeptide molecule is produced by a host cell or organisms of the same species, preferably of the same variety or strain. If homologous to a host cell, a nucleic acid sequence encoding a polypeptide will typically (but not necessarily) be operably linked to another (heterologous) promoter sequence and, if applicable, another (heterologous) secretory signal sequence and/or terminator sequence than in its natural environment. It is understood that the regulatory sequences, signal sequences, terminator sequences, etc. may also be homologous to the host cell. In this context, the use of only “homologous” sequence elements allows the construction of “self-cloned” genetically modified organisms (GMO's) (self-cloning is defined herein as in European Directive 98/81/EC Annex II). When used to indicate the relatedness of two nucleic acid sequences the term “homologous” means that one single-stranded nucleic acid sequence may hybridize to a complementary single-stranded nucleic acid sequence. The degree of hybridization may depend on a number of factors including the amount of identity between the sequences and the hybridization conditions such as temperature and salt concentration as discussed later.
The term “heterologous” when used with respect to a nucleic acid (DNA or RNA) or protein refers to a nucleic acid or protein that does not occur naturally as part of the organism, cell, genome or DNA or RNA sequence in which it is present, or that is found in a cell or location or locations in the genome or DNA or RNA sequence that differ from that in which it is found in nature. Heterologous nucleic acids or proteins are not endogenous to the cell into which it is introduced, but has been obtained from another cell or synthetically or recombinantly produced. Generally, though not necessarily, such nucleic acids encode proteins that are not normally produced by the cell in which the DNA is transcribed or expressed. Similarly exogenous RNA encodes for proteins not normally expressed in the cell in which the exogenous RNA is present. Heterologous nucleic acids and proteins may also be referred to as foreign nucleic acids or proteins. Any nucleic acid or protein that one of skill in the art would recognize as heterologous or foreign to the cell in which it is expressed is herein encompassed by the term heterologous nucleic acid or protein. The term heterologous also applies to non-natural combinations of nucleic acid or amino acid sequences, i.e. combinations where at least two of the combined sequences are foreign with respect to each other.
To date some 450 xylose isomerase amino acid sequences are publicly available in Genbank and other sequence databases. Among them are a number of amino acid sequences of xylose isomerases that are known for the ability of functional expression in yeasts, including e.g. xylose isomerases from anaerobic fungi such Piromyces, Cyllamyces, and Orpinomyces, as well as bacterial xylose isomerases from Bacteroides, all of which share more than 70% amino acid sequence identity with the Piromyces enzyme. The present inventors have now surprisingly found amino acid sequences of xylose isomerases that are not related to the Piromyces enzyme in the sense that they share less than 70% amino acid sequence identity with the amino acid sequence of Piromyces enzyme, and that nonetheless have the ability of functional (i.e. active) expression in yeasts. Furthermore, the present inventors have identified a number of amino acid sequence elements that are shared among all xylose isomerases with the ability of functional expression in yeasts. Functional expression of a xylose isomerase in a yeast is herein understood as expression of a codon-optimised coding sequence for a xylose isomerase from a glycolytic promoter on a 2μ-based plasmid in S. cerevisiae that allows the detectable growth of the yeast on xylose as sole carbon source, preferably under anaerobic conditions with production of ethanol at the expense of xylose, more preferably with at least one of a growth rate, biomass and ethanol yield that is at least 10, 20, 50 or 80% of that achieved with a codon-optimised Piromyces xylose isomerase coding sequence under otherwise identical conditions. Preferably functional expression is expression that allows the detectable growth of the yeast on xylose as sole carbon source at a temperature which is lower than 35, 33, 30 or 28° C. and at a temperature which is higher than 20, 22, or 25° C.
In a first aspect the present invention relates to a transformed host cell that has the ability of isomerising xylose to xylulose. The ability of isomerising xylose to xylulose is conferred to the host cell by transformation of the host cell with a nucleic acid construct comprising a nucleotide sequence encoding a xylose isomerase. The transformed host cell's ability to isomerise xylose into xylulose is understood to mean the direct isomerisation of xylose, in a single reaction catalysed by a xylose isomerase, to xylulose, as opposed to the two step conversion of xylose into xylulose via a xylitol intermediate as catalysed by xylose reductase and xylitol dehydrogenase, respectively.
In one embodiment the nucleotide sequence encoding the xylose isomerase is selected from the group consisting of:
In one embodiment the nucleotide sequence encoding the xylose isomerase encodes an amino acid sequence comprising one or amino acid sequence elements that are shared among xylose isomerases with the ability of functional expression in yeasts. In this embodiment the nucleotide sequence encoding the xylose isomerase encodes an amino acid sequence comprising one or amino acid sequence elements selected from the group consisting of:
In this embodiment the encoded xylose isomerase may comprise at least 1, 2, 3, 4, 5, 6, 7 or all 8 of the elements (a)-(h) in all possible combinations. Thus, in this embodiment the encoded xylose isomerase may comprise the following element or combinations of elements: (a); (b); (c); (d); (e); (f); (g); (h); (a) and (b); (a) and (c); (a) and (d); (a) and (e); (a) and (f); (a) and (g); (a) and (h); (b) and (c); (b) and (d); (b) and (e); (b) and (f); (b) and (g); (b) and (h); (c) and (d); (c) and (e); (c) and (f); (c) and (g); (c) and (h); (d) and (e); (d) and (f); (d) and (g); (d) and (h); (e) and (f); (e) and (g); (e) and (h); (f) and (g); (f) and (h); (g) and (h); (a), (b) and (c); (a), (b) and (d); (a), (b) and (e); (a), (b) and (f); (a), (b) and (g); (a), (b) and (h); (a), (c) and (d); (a), (c) and (e); (a), (c) and (f); (a), (c) and (g); (a), (c) and (h); (a), (d) and (e); (a), (d) and (f); (a), (d) and (g); (a), (d) and (h); (a), (e) and (f); (a), (e) and (g); (a), (e) and (h); (a), (f) and (g); (a), (f) and (h); (a), (g) and (h); (b), (c) and (d); (b), (c) and (e); (b), (c) and (f); (b), (c) and (g); (b), (c) and (h); (b), (d) and (c); (b), (d) and (f); (b), (d) and (g); (b), (d) and (h); (b), (c) and (f); (b), (c) and (g); (b), (c) and (h); (b), (f) and (g); (b), (f) and (h); (b), (g) and (h); (c), (d) and (c); (c), (d) and (f); (c), (d) and (g); (c), (d) and (h); (c), (c) and (f); (c), (c) and (g); (c), (c) and (h); (c), (f) and (g); (c), (f) and (h); (c), (g) and (h); (d), (c) and (f); (d), (e) and (g); (d), (e) and (h); (d), (f) and (g); (d), (f) and (h); (d), (g) and (h); (e), (f) and (g); (e), (f) and (h); (e), (g) and (h); (f), (g) and (h); (a), (b), (c) and (d); (a), (b), (c) and (e); (a), (b), (c) and (f); (a), (b), (c) and (g); (a), (b), (c) and (h); (a), (b), (d) and (e); (a), (b), (d) and (f); (a), (b), (d) and (g); (a), (b), (d) and (h); (a), (b), (e) and (f); (a), (b), (e) and (g); (a), (b), (e) and (h); (a), (b), (f) and (g); (a), (b), (f) and (h); (a), (b), (g) and (h); (a), (c), (d) and (e); (a), (c), (d) and (f); (a), (c), (d) and (g); (a), (c), (d) and (h); (a), (c), (e) and (f); (a), (c), (e) and (g); (a), (c), (e) and (h); (a), (c), (f) and (g); (a), (c), (f) and (h); (a), (c), (g) and (h); (a), (d), (e) and (f); (a), (d), (e) and (g); (a), (d), (e) and (h); (a), (d), (f) and (g); (a), (d), (f) and (h); (a), (d), (g) and (h); (a), (e), (f) and (g); (a), (e), (f) and (h); (a), (e), (g) and (h); (a), (f), (g) and (h); (b), (c), (d) and (e); (b), (c), (d) and (f); (b), (c), (d) and (g); (b), (c), (d) and (h); (b), (c), (e) and (f); (b), (c), (e) and (g); (b), (c), (e) and (h); (b), (c), (f) and (g); (b), (c), (f) and (h); (b), (c), (g) and (h); (b), (d), (e) and (f); (b), (d), (e) and (g); (b), (d), (e) and (h); (b), (d), (f) and (g); (b), (d), (f) and (h); (b), (d), (g) and (h); (b), (e), (f) and (g); (b), (e), (f) and (h); (b), (e), (g) and (h); (b), (f), (g) and (h); (c), (d), (e) and (f); (c), (d), (e) and (g); (c), (d), (e) and (h); (c), (d), (f) and (g); (c), (d), (f) and (h); (c), (d), (g) and (h); (c), (e), (f) and (g); (c), (e), (f) and (h); (c), (e), (g) and (h); (c), (f), (g) and (h); (d), (e), (f) and (g); (d), (e), (f) and (h); (d), (e), (g) and (h); (d), (f), (g) and (h); (e), (f), (g) and (h); (a), (b), (c), (d) and (e); (a), (b), (c), (d) and (f); (a), (b), (c), (d) and (g); (a), (b), (c), (d) and (h); (a), (b), (c), (e) and (f); (a), (b), (c), (e) and (g); (a), (b), (c), (e) and (h); (a), (b), (c), (f) and (g); (a), (b), (c), (f) and (h); (a), (b), (c), (g) and (h); (a), (b), (d), (e) and (f); (a), (b), (d), (e) and (g); (a), (b), (d), (e) and (h); (a), (b), (d), (f) and (g); (a), (b), (d), (f) and (h); (a), (b), (d), (g) and (h); (a), (b), (e), (f) and (g); (a), (b), (e), (f) and (h); (a), (b), (e), (g) and (h); (a), (b), (f), (g) and (h); (a), (c), (d), (e) and (f); (a), (c), (d), (e) and (g); (a), (c), (d), (e) and (h); (a), (c), (d), (f) and (g); (a), (c), (d), (f) and (h); (a), (c), (d), (g) and (h); (a), (c), (e), (f) and (g); (a), (c), (e), (f) and (h); (a), (c), (e), (g) and (h); (a), (c), (f), (g) and (h); (a), (d), (e), (f) and (g); (a), (d), (e), (f) and (h); (a), (d), (e), (g) and (h); (a), (d), (f), (g) and (h); (a), (e), (f), (g) and (h); (b), (c), (d), (e) and (f); (b), (c), (d), (e) and (g); (b), (c), (d), (e) and (h); (b), (c), (d), (f) and (g); (b), (c), (d), (f) and (h); (b), (c), (d), (g) and (h); (b), (c), (e), (f) and (g); (b), (c), (c), (f) and (h); (b), (c), (c), (g) and (h); (b), (c), (f), (g) and (h); (b), (d), (c), (f) and (g); (b), (d), (c), (f) and (h); (b), (d), (c), (g) and (h); (b), (d), (f), (g) and (h); (b), (c), (f), (g) and (h); (c), (d), (c), (f) and (g); (c), (d), (c), (f) and (h); (c), (d), (c), (g) and (h); (c), (d), (f), (g) and (h); (c), (c), (f), (g) and (h); (d), (c), (f), (g) and (h); (a), (b), (c), (d), (e) and (f); (a), (b), (c), (d), (e) and (g); (a), (b), (c), (d), (e) and (h); (a), (b), (c), (d), (f) and (g); (a), (b), (c), (d), (f) and (h); (a), (b), (c), (d), (g) and (h); (a), (b), (c), (e), (f) and (g); (a), (b), (c), (e), (f) and (h); (a), (b), (c), (e), (g) and (h); (a), (b), (c), (f), (g) and (h); (a), (b), (d), (e), (f) and (g); (a), (b), (d), (e), (f) and (h); (a), (b), (d), (e), (g) and (h); (a), (b), (d), (f), (g) and (h); (a), (b), (e), (f), (g) and (h); (a), (c), (d), (e), (f) and (g); (a), (c), (d), (e), (f) and (h); (a), (c), (d), (e), (g) and (h); (a), (c), (d), (f), (g) and (h); (a), (c), (e), (f), (g) and (h); (a), (d), (e), (f), (g) and (h); (b), (c), (d), (e), (f) and (g); (b), (c), (d), (e), (f) and (h); (b), (c), (d), (e), (g) and (h); (b), (c), (d), (f), (g) and (h); (b), (c), (e), (f), (g) and (h); (b), (d), (e), (f), (g) and (h); (c), (d), (e), (f), (g) and (h); (a), (b), (c), (d), (e), (f) and (g); (a), (b), (c), (d), (e), (f) and (h); (a), (b), (c), (d), (e), (g) and (h); (a), (b), (c), (d), (f), (g) and (h); (a), (b), (c), (e), (f), (g) and (h); (a), (b), (d), (e), (f), (g) and (h); (a), (c), (d), (e), (f), (g) and (h); and finally, (b), (c), (d), (e), (f), (g) and (h). Furthermore, amino acid sequences in positions corresponding to those of amino acid sequences in (b), (d), (e) and (f) may differ preferably in no more than 1, 2, or 3 amino acid from the amino acid sequences in (b), (d), (e) and (f). Preferably, element (b) at least consists of I at position 136; element (d) at least consists of F at position 264; element (f) at least consists of an F or a Y at position 391. In one preferred embodiment, the encoded xylose isomerase comprises at least one of elements (a), (f), (g) and (h), More preferably, the encoded xylose isomerase in addition comprises at least one of elements (b) and (c) and most preferably the encoded xylose isomerase in addition comprises at least one of elements (d) and (e). In one preferred embodiment, the encoded xylose isomerase comprises at least element (a), more preferably in addition the isomerise comprises at least elements (b), (c) and/or (g), still more preferably in addition the isomerise comprises at least elements (d), (f) and/or (h), most preferably the isomerise additionally comprises element (e).
Amino acid positions of the above sequence elements (a)-(h) refer to positions in the reference amino acid sequence of the Piromyces xylose isomerase of SEQ ID NO: 3. In amino acid sequences of the invention other than SEQ ID NO: 3, preferably, the amino acid positions of sequence elements (a)-(h) are present in amino acid positions corresponding to the positions of sequence elements (a)-(h) in SEQ ID NO: 3, preferably in a ClustalW (1.83) sequence alignment using default settings. The skilled person will know how to identify corresponding amino acid positions in xylose isomerase amino acid sequences other than SEQ ID NO: 3 using amino acid sequence alignment algorithms as defined hereinabove. An example of such an alignment is depicted in Table 4, which shows a Clustal W (1.83) multiple sequence alignment of xylose isomerase amino acid sequences from organisms indicated on the left. The shaded amino acids the Piromyces sequence (SEQ ID NO: 3) in Table 4 indicate sequence elements that are shared among xylose isomerases that have the ability of functional expression in yeast.
In one embodiment the nucleotide sequence encoding the xylose isomerase encodes an amino acid sequence that is not one or more of SEQ ID NO: 3-7. Preferably the nucleotide sequence encoding the xylose isomerase does not have an amino acid sequence that has more than (or has an amino acid sequence that has less than) 99, 98, 97, 96, 95, 94, 93, 92, 91, 90, 89, 88, 87, 86, 85, 84, 83, 82, 81, 80, 79, 78, 77, 76, 75, 74, 73, 72, 71 or 70% sequence identity with at least one amino acid sequence selected from the group consisting of SEQ ID NO: 3-7.
In one embodiment the nucleotide sequence encoding the xylose isomerase encodes an amino acid sequence that is not one or more of SEQ ID NO: 35. Preferably the nucleotide sequence encoding the xylose isomerase does not have an amino acid sequence that has more than (or has an amino acid sequence that has less than) 99, 98, 97, 96, 95, 94, 93, 92, 91, 90, 89, 88, 87, 86, 85, 84, 83, 82, 81, 80, 79, 78, 77, 76, 75, 74, 73, 72, 71 or 70% sequence identity with at least one amino acid sequence selected from the group consisting of SEQ ID NO: 35.
In one embodiment the nucleotide sequence encoding the xylose isomerase encodes an amino acid sequence that is not an amino acid sequences selected from the group consisting of:
Preferably the nucleotide sequence encoding the xylose isomerase does not have an amino acid sequence that has more than (or has an amino acid sequence that has less than) 99, 98, 97, 96, 95, 94, 93, 92, 91, 90, 89, 88, 87, 86, 85, 84, 83, 82, 81, 80, 79, 78, 77, 76, 75, 74, 73, 72, 71 or 70% sequence identity with at least one amino acid sequence selected from the group consisting of:
In one embodiment the nucleotide sequence encoding the xylose isomerase encodes an amino acid sequence that is not an amino acid of a xylose isomerase from an anaerobic fungus of the Family Neocallimastigaceae, such as a fungus from a genus selected from the group consisting of: Anaeromyces, Caecomyces, Cyllamyces, Neocallimastix, Orpinomyces, Piromyces, and Ruminomyces.
In one embodiment the nucleotide sequence encoding the xylose isomerase encodes an amino acid sequence that is not an amino acid of a xylose isomerase from a bacterium from the genus Bacteroides or Parabacteroides.
The nucleotide sequences of the invention encode a novel class of xylose isomerases that may be functionally expressed in eukaryotic microbial host cells of the invention as defined below. The nucleotide sequences of the invention preferably encode xylose isomerases that naturally occurs in certain fungi, bacteria and tunicate.
A preferred nucleotide sequence of the invention thus encodes a xylose isomerase with an amino acid sequence that is identical to that of a xylose isomerase that is obtainable from (or naturally occurs in) a bacterium of the Family Clostridiaceae, more preferably a bacterium of the genus Clostridium, of which C. difficile is most preferred.
A preferred nucleotide sequence of the invention thus encodes a xylose isomerase with an amino acid sequence that is identical to that of a xylose isomerase that is obtainable from (or naturally occurs in) a bacterium of the Family Fusobacteriaceae, more preferably a bacterium of the genus Fusobacterium, of which F. mortiferum is most preferred.
A preferred nucleotide sequence of the invention thus encodes a xylose isomerase with an amino acid sequence that is identical to that of a xylose isomerase that is obtainable from (or naturally occurs in) a tunicate, preferably a tunicate of the Family Cionidae, more preferably a tunicate of the genus Ciona, of which C. intestinales is most preferred.
In another embodiment the nucleotide sequence encoding the xylose isomerase is selected from the group consisting of:
It is however understood that nucleotide sequences encoding engineered forms of any of the xylose isomerases defined above and that comprise one or more amino acid substitutions, insertions and/or deletions as compared to the corresponding naturally occurring xylose isomerases but that are within the ranges of identity or similarity as defined herein are expressly included in the invention. Therefore, in one embodiment the nucleotide sequence of the invention encodes a xylose isomerase amino acid sequence comprising a xylose isomerase signature sequence as defined by Meaden et al. (1994, Gene, 141: 97-101): VXW{GP}GREG{YSTA} (SEQ ID NO:39) (corresponding to positions 187-195 of SEQ ID NO:3) and {LIVM}EPKPX{EQ}P (SEQ ID N0:40) (corresponding to positions 232-239 of SEQ ID NO:3), wherein “X” can be any amino acid and wherein one of the amino acids in braces can be present at that position in the signature sequence. A xylose isomerase amino acid sequence of the invention further preferably comprises the conserved amino acid residues His-102, Asp-105, and Asp-340, which constitute a triad directly involved in catalysis, Lys-235 plays a structural as well as a functional catalytic role, and Glu-233, which is involved in binding of the magnesium (Vangrysperre et al., 1990, Biochem. J. 265: 699-705; Henrick et al., J. Mol. Biol. 208: 129-157; Bhosale et al., 1996 Microbiol. Rev. 60: 280-300) Amino acid positions of the above signature sequences and conserved residues refer to positions in the reference amino acid sequence of the Piromyces xylose isomerase of SEQ ID NO: 3. In amino acid sequences of the invention other than SEQ ID NO: 3, preferably, the amino acid positions of the above signature sequences and conserved residues are present in amino acid positions corresponding to the positions of the signature sequences and conserved residues in SEQ ID NO: 3, preferably in a ClustalW (1.83 or 1.81) sequence alignment using default settings. The skilled person will know how to identify corresponding amino acid positions in xylose isomerase amino acid sequences other than SEQ ID NO: 3 using amino acid sequence alignment algorithms as defined hereinabove. An example of such an alignment is depicted in Table 4. In addition, to date some 450 amino acid sequences of xylose isomerases are known in the art and new ones are added continuously being added. Sequence alignments of SEQ ID NO: 3 and the xylose isomerase sequences of the invention with these known and new xylose isomerase amino acid sequences will indicate further conserved regions and amino acid positions, the conservation of which are important for structure and enzymatic activity. These regions and positions will tolerate no or only conservative amino acid substitutions Amino acid substitutions outside of these regions and positions are unlikely to greatly affect xylose isomerase activity.
The nucleotide sequence encodes a xylose isomerase that is preferably expressed in active form in the transformed host cell. Thus, expression of the nucleotide sequence in the host cell produces a xylose isomerase with a specific activity of at least 10 U xylose isomerase activity per mg protein at 25° C., preferably at least 20, 25, 30, 50, 100, 200 or 300 U per mg at 25° C. The specific activity of the xylose isomerase expressed in the transformed host cell is herein defined as the amount of xylose isomerase activity units per mg protein of cell free lysate of the host cell, e.g. a yeast cell free lysate. Determination of the xylose isomerase activity, amount of protein and preparation of the cell free lysate are as described in the Examples. Preferably, expression of the nucleotide sequence in the host cell produces a xylose isomerase with a Km for xylose that is less than 50, 40, 30 or 25 mM, more preferably, the Km for xylose is about 20 mM or less.
The nucleotide sequences of the invention, encoding polypeptides with xylose isomerase activity, are obtainable from genomic and/or cDNA of a fungus, yeast or bacterium that belongs to a phylum, class or genus as described above, using method for isolation of nucleotide sequences that are well known in the art per se (see e.g. Sambrook and Russell (2001) “Molecular Cloning: A Laboratory Manual (3rd edition), Cold Spring Harbor Laboratory, Cold Spring Harbor Laboratory Press, New York). The nucleotide sequences of the invention are e.g. obtainable in a process wherein a) degenerate PCR primers (such as those in SEQ ID NO.'s 14 and 15) are used on genomic and/or cDNA of a suitable organism (e.g. a fungus, bacterium or tunicate as indicated above) to generate a PCR fragment comprising part of the nucleotide sequences encoding the polypeptides with xylose isomerase activity; b) the PCR fragment obtained in a) is used as probe to screen a cDNA and/or genomic library of the organism; and c) producing a cDNA or genomic DNA comprising the nucleotide sequence encoding a polypeptide with xylose isomerase activity.
To increase the likelihood that the xylose isomerase is expressed at sufficient levels and in active form in the transformed host cells of the invention, the nucleotide sequence encoding these enzymes, as well as other enzymes of the invention (see below), are preferably adapted to optimise their codon usage to that of the host cell in question. The adaptiveness of a nucleotide sequence encoding an enzyme to the codon usage of a host cell may be expressed as codon adaptation index (CAI). The codon adaptation index is herein defined as a measurement of the relative adaptiveness of the codon usage of a gene towards the codon usage of highly expressed genes in a particular host cell or organism. The relative adaptiveness (w) of each codon is the ratio of the usage of each codon, to that of the most abundant codon for the same amino acid. The CAI index is defined as the geometric mean of these relative adaptiveness values. Non-synonymous codons and termination codons (dependent on genetic code) are excluded. CAI values range from 0 to 1, with higher values indicating a higher proportion of the most abundant codons (see Sharp and Li, 1987, Nucleic Acids Research 15: 1281-1295; also see: Jansen et al., 2003, Nucleic Acids Res. 31(8):2242-51). An adapted nucleotide sequence preferably has a CAI of at least 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8 or 0.9. Most preferred are the sequences as listed in SEQ ID NO's: 16, 17 and 38, which have been codon optimised for expression in S. cerevisiae cells.
The host cell to be transformed with a nucleic acid construct comprising a nucleotide sequence encoding a xylose isomerase of the invention preferably is a eukaryotic microbial host, more preferably a fungal host cell, such as a yeast or filamentous fungal host cell. Preferably the host cell is a cultured cell. The host cell of the invention, preferably is a host capable of active or passive pentose (xylose and preferably also arabinose) transport into the cell. The host cell preferably contains active glycolysis. The host cell may further preferably contains an endogenous pentose phosphate pathway and may contain endogenous xylulose kinase activity so that xylulose isomerised from xylose may be metabolised to pyruvate. The host further preferably contains enzymes for conversion of a pentose (preferably through pyruvate) to a desired fermentation product such as ethanol, lactic acid, 3-hydroxy-propionic acid, acrylic acid, acetic acid, succinic acid, citric acid, amino acids, 1,3-propane-diol, ethylene, glycerol, β-lactam antibiotics and cephalosporins. A particularly preferred host cell is a host cell that is naturally capable of alcoholic fermentation, preferably, anaerobic alcoholic fermentation. The host cell further preferably has a high tolerance to ethanol, a high tolerance to low pH (i.e. capable of growth at a pH lower than 5, 4, or 3) and towards organic acids like lactic acid, acetic acid or formic acid and sugar degradation products such as furfural and hydroxy-methylfurfural, and a high tolerance to elevated temperatures. Any of these characteristics or activities of the host cell may be naturally present in the host cell or may be introduced or modified by genetic modification, preferably by self cloning or by the methods of the invention described below. A suitable cell is a cultured cell, a cell that may be cultured in fermentation process e.g. in submerged or solid state fermentation. Particularly suitable cells are eukaryotic microorganism like e.g. fungi, however, most suitable for use in the present inventions are yeasts or filamentous fungi.
Yeasts are herein defined as eukaryotic microorganisms and include all species of the subdivision Eumycotina (Yeasts: characteristics and identification, J. A. Barnett, R. W. Payne, D. Yarrow, 2000, 3rd ed., Cambridge University Press, Cambridge UK; and, The yeasts, a taxonomic study, C. P. Kurtzman and J. W. Fell (eds) 1998, 4th ed., Elsevier Science Publ. B.V., Amsterdam, The Netherlands) that predominantly grow in unicellular form. Yeasts may either grow by budding of a unicellular thallus or may grow by fission of the organism. Preferred yeasts as host cells belong to the genera Saccharomyces, Kluyveromyces, Candida, Pichia, Schizosaccharomyces, Hansenula, Kloeckera, Schwanniomyces, and Yarrowia. Preferably the yeast is capable of anaerobic fermentation, more preferably anaerobic alcoholic fermentation. Over the years suggestions have been made for the introduction of various organisms for the production of bio-ethanol from crop sugars. In practice, however, all major bio-ethanol production processes have continued to use the yeasts of the genus Saccharomyces as ethanol producer. This is due to the many attractive features of Saccharomyces species for industrial processes, i.e., a high acid-, ethanol- and osmo-tolerance, capability of anaerobic growth, and of course its high alcoholic fermentative capacity. Preferred yeast species as fungal host cells include S. cerevisiae, S. exiguus, S. bayanus, K. lactis, K. marxianus and Schizosaccharomyces pombe.
Filamentous fungi are herein defined as eukaryotic microorganisms that include all filamentous forms of the subdivision Eumycotina. These fungi are characterized by a vegetative mycelium composed of chitin, cellulose, and other complex polysaccharides. The filamentous fungi of the present invention are morphologically, physiologically, and genetically distinct from yeasts. Vegetative growth by filamentous fungi is by hyphal elongation and carbon catabolism of most filamentous fungi is obligately aerobic. Preferred filamentous fungi as host cells belong to the genera Aspergillus, Trichoderma, Humicola, Acremonium, Fusarium, and Penicillium.
In a transformed host cell of the invention, the nucleotide sequence encoding the xylose isomerase as defined above is preferably operably linked to a promoter that causes sufficient expression of the nucleotide sequences in the cell to confer to the cell the ability to convert xylose into xylulose. More preferably the promoter causes sufficient expression of the nucleotide sequences to confer to the cell the ability to grow on xylose as sole carbon and/or energy source, most preferably under anaerobic conditions. Suitable promoters for expression of the nucleotide sequence as defined above include promoters that are insensitive to catabolite (glucose) repression and/or that do require xylose for induction. Promoters having these characteristics are widely available and known to the skilled person. Suitable examples of such promoters include e.g. promoters from glycolytic genes such as the phosphofructokinase (PPK), triose phosphate isomerase (TPI), glyceraldehyde-3-phosphate dehydrogenase (GPD, TDH3 or GAPDH), pyruvate kinase (PYK), phosphoglycerate kinase (PGK), glucose-6-phosphate isomerase promoter (PGII) promoters from yeasts or filamentous fungi; more details about such promoters from yeast may be found in (WO 93/03159). Other useful promoters are ribosomal protein encoding gene promoters, the lactase gene promoter (LAC4), alcohol dehydrogenase promoters (ADH1, ADH4, and the like), the enolase promoter (ENO), the hexose(glucose) transporter promoter (HXT7), and the cytochrome c1 promoter (CYC1). Other promoters, both constitutive and inducible, and enhancers or upstream activating sequences will be known to those of skill in the art. Preferably the promoter that is operably linked to nucleotide sequence as defined above is homologous to the host cell.
The transformed host cell of the invention further preferably comprises xylulose kinase activity so that xylulose isomerised from xylose may be metabolised to pyruvate. Preferably, the cell contains endogenous xylulose kinase activity. More preferably, a cell of the invention comprises a genetic modification that increases the specific xylulose kinase activity. Preferably the genetic modification causes overexpression of a xylulose kinase, e.g. by overexpression of a nucleotide sequence encoding a xylulose kinase. The gene encoding the xylulose kinase may be endogenous to the cell or may be a xylulose kinase that is heterologous to the cell. A nucleotide sequence that may be used for overexpression of xylulose kinase in the cells of the invention is e.g. the xylulose kinase gene from S. cerevisiae (XKS1) as described by Deng and Ho (1990, Appl. Biochem. Biotechnol. 24-25: 193-199). Another preferred xylulose kinase is a xylose kinase that is related to the xylulose kinase from Piromyces (xylB; see WO 03/0624430). This Piromyces xylulose kinase is actually more related to prokaryotic kinase than to all of the known eukaryotic kinases such as the yeast kinase. The eukaryotic xylulose kinases have been indicated as non-specific sugar kinases, which have a broad substrate range that includes xylulose. In contrast, the prokaryotic xylulose kinases, to which the Piromyces kinase is most closely related, have been indicated to be more specific kinases for xylulose, i.e. having a narrower substrate range. In the cells of the invention, a xylulose kinase to be overexpressed is overexpressed by at least a factor 1.1, 1.2, 1.5, 2, 5, 10 or 20 as compared to a strain which is genetically identical except for the genetic modification causing the overexpression. It is to be understood that these levels of overexpression may apply to the steady state level of the enzyme's activity, the steady state level of the enzyme's protein as well as to the steady state level of the transcript coding for the enzyme.
A cell of the invention further preferably comprises a genetic modification that increases the flux of the pentose phosphate pathway as described in WO 06/009434. In particular, the genetic modification causes an increased flux of the non-oxidative part pentose phosphate pathway. A genetic modification that causes an increased flux of the non-oxidative part of the pentose phosphate pathway is herein understood to mean a modification that increases the flux by at least a factor 1.1, 1.2, 1.5, 2, 5, 10 or 20 as compared to the flux in a strain which is genetically identical except for the genetic modification causing the increased flux. The flux of the non-oxidative part of the pentose phosphate pathway may be measured as described in WO 06/009434.
Genetic modifications that increase the flux of the pentose phosphate pathway may be introduced in the cells of the invention in various ways. These including e.g. achieving higher steady state activity levels of xylulose kinase and/or one or more of the enzymes of the non-oxidative part pentose phosphate pathway and/or a reduced steady state level of unspecific aldose reductase activity. These changes in steady state activity levels may be effected by selection of mutants (spontaneous or induced by chemicals or radiation) and/or by recombinant DNA technology e.g. by overexpression or inactivation, respectively, of genes encoding the enzymes or factors regulating these genes.
In a preferred cell of the invention, the genetic modification comprises overexpression of at least one enzyme of the (non-oxidative part) pentose phosphate pathway. Preferably the enzyme is selected from the group consisting of the enzymes encoding for ribulose-5-phosphate isomerase, ribulose-5-phosphate 3-epimerase, transketolase and transaldolase. Various combinations of enzymes of the (non-oxidative part) pentose phosphate pathway may be overexpressed. E.g. the enzymes that are overexpressed may be at least the enzymes ribulose-5-phosphate isomerase and ribulose-5-phosphate 3-epimerase; or at least the enzymes ribulose-5-phosphate isomerase and transketolase; or at least the enzymes ribulose-5-phosphate isomerase and transaldolase; or at least the enzymes ribulose-5-phosphate 3-epimerase and transketolase; or at least the enzymes ribulose-5-phosphate 3-epimerase and transaldolase; or at least the enzymes transketolase and transaldolase; or at least the enzymes ribulose-5-phosphate 3-epimerase, transketolase and transaldolase; or at least the enzymes ribulose-5-phosphate isomerase, transketolase and transaldolase; or at least the enzymes ribulose-5-phosphate isomerase, ribulose-5-phosphate 3-epimerase, and transaldolase; or at least the enzymes ribulose-5-phosphate isomerase, ribulose-5-phosphate 3-epimerase, and transketolase. In one embodiment of the invention each of the enzymes ribulose-5-phosphate isomerase, ribulose-5-phosphate 3-epimerase, transketolase and transaldolase are overexpressed in the cell of the invention. Preferred is a cell in which the genetic modification comprises at least overexpression of the enzyme transaldolase. More preferred is a cell in which the genetic modification comprises at least overexpression of both the enzymes transketolase and transaldolase as such a host cell is already capable of anaerobic growth on xylose. In fact, under some conditions we have found that cells overexpressing only the transketolase and the transaldolase already have the same anaerobic growth rate on xylose as do cells that overexpress all four of the enzymes, i.e. the ribulose-5-phosphate isomerase, ribulose-5-phosphate 3-epimerase, transketolase and transaldolase. Moreover, cells of the invention overexpressing both of the enzymes ribulose-5-phosphate isomerase and ribulose-5-phosphate 3-epimerase are preferred over cells overexpressing only the isomerase or only the 3-epimerase as overexpression of only one of these enzymes may produce metabolic imbalances.
There are various means available in the art for overexpression of enzymes in the cells of the invention. In particular, an enzyme may be overexpressed by increasing the copynumber of the gene coding for the enzyme in the cell, e.g. by integrating additional copies of the gene in the cell's genome, by expressing the gene from an episomal multicopy expression vector or by introducing a episomal expression vector that comprises multiple copies of the gene. The coding sequence used for overexpression of the enzymes preferably is homologous to the host cell of the invention. However, coding sequences that are heterologous to the host cell of the invention may likewise be applied.
Alternatively overexpression of enzymes in the cells of the invention may be achieved by using a promoter that is not native to the sequence coding for the enzyme to be overexpressed, i.e. a promoter that is heterologous to the coding sequence to which it is operably linked. Although the promoter preferably is heterologous to the coding sequence to which it is operably linked, it is also preferred that the promoter is homologous, i.e. endogenous to the cell of the invention. Preferably the heterologous promoter is capable of producing a higher steady state level of the transcript comprising the coding sequence (or is capable of producing more transcript molecules, i.e. mRNA molecules, per unit of time) than is the promoter that is native to the coding sequence, preferably under conditions where xylose or xylose and glucose are available as carbon sources, more preferably as major carbon sources (i.e. more than 50% of the available carbon source consists of xylose or xylose and glucose), most preferably as sole carbon sources. Suitable promoters in this context include promoters as described above for expression of the nucleotide sequences encoding xylose isomerases as defined above.
A further preferred cell of the invention comprises a genetic modification that reduces unspecific aldose reductase activity in the cell. Preferably, unspecific aldose reductase activity is reduced in the host cell by one or more genetic modifications that reduce the expression of or inactivates a gene encoding an unspecific aldose reductase. Preferably, the genetic modifications reduce or inactivate the expression of each endogenous copy of a gene encoding an unspecific aldose reductase that is capable of reducing an aldopentose, including, xylose, xylulose and arabinose, in the cell's genome. A given cell may comprise multiple copies of genes encoding unspecific aldose reductases as a result of di-, poly- or aneu-ploidy, and/or a cell may contain several different (iso)enzymes with aldose reductase activity that differ in amino acid sequence and that are each encoded by a different gene. Also in such instances preferably the expression of each gene that encodes an unspecific aldose reductase is reduced or inactivated. Preferably, the gene is inactivated by deletion of at least part of the gene or by disruption of the gene, whereby in this context the term gene also includes any non-coding sequence up- or down-stream of the coding sequence, the (partial) deletion or inactivation of which results in a reduction of expression of unspecific aldose reductase activity in the host cell. A nucleotide sequence encoding an aldose reductase whose activity is to be reduced in the cell of the invention and amino acid sequences of such aldose reductases are described in WO 06/009434 and include e.g. the (unspecific) aldose reductase genes of S. cerevisiae GRE3 gene (Träff et al., 2001, Appl. Environm. Microbiol. 67: 5668-5674) and orthologues thereof in other species.
In a further preferred embodiment, the transformed cell of the invention that has the ability of isomerising xylose to xylulose as described above, in addition has the ability to convert L-arabinose into D-xylulose 5-phosphate as e.g. described in Wisselink et al. (2007, AEM Accepts, published online ahead of print on 1 Jun. 2007; Appl. Environ. Microbiol. doi:10.1128/AEM.00177-07) and in EP 1 499 708. The ability of to converting L-arabinose into D-xylulose 5-phosphate is preferably conferred to the cell by transformation with a nucleic acid construct(s) comprising nucleotide sequences encoding a) an arabinose isomerase; b) a ribulokinase, preferably a L-ribulokinase a xylose isomerase; and c) a ribulose-5-P-4-epimerase, preferably a L-ribulose-5-P-4-epimerase. Preferably, in the cells of the invention, the ability to convert L-arabinose into D-xylulose 5-phosphate is the ability to convert L-arabinose into D-xylulose 5-phosphate through the subsequent reactions of 1) isomerisation of arabinose into ribulose; 2) phosphorylation of ribulose to ribulose 5-phosphate; and, 3) epimerisation of ribulose 5-phosphate into D-xylulose 5-phosphate. Suitable nucleotide sequences encoding arabinose isomerases, a ribulokinases and ribulose-5-P-4-epimerases may be obtained from Bacillus subtilis, Escherichia coli (sec e.g. EP 1 499 708), Lactobacilli, e.g. Lactobacillus plantarum (see e.g. Wisselink et al. supra), or species of Clavibacter, Arthrobacter and Gramella, of which preferably Clavibacter michiganensis, Arthrobacter aurescens and Gramella forsetii.
A further preferred transformed host cell according to the invention may comprises further genetic modifications that result in one or more of the characteristics selected from the group consisting of (a) increased transport of xylose and/or arabinose into the cell; (b) decreased sensitivity to catabolite repression; (c) increased tolerance to ethanol, osmolarity or organic acids; and, (d) reduced production of by-products. By-products are understood to mean carbon-containing molecules other than the desired fermentation product and include e.g. xylitol, arabinitol, glycerol and/or acetic acid. Any genetic modification described herein may be introduced by classical mutagenesis and screening and/or selection for the desired mutant, or simply by screening and/or selection for the spontaneous mutants with the desired characteristics. Alternatively, the genetic modifications may consist of overexpression of endogenous genes and/or the inactivation of endogenous genes. Genes the overexpression of which is desired for increased transport of arabinose and/or xylose into the cell are preferably chosen form genes encoding a hexose or pentose transporter. In S. cerevisiae and other yeasts these genes include HXT1, HXT2, HXT4, HXT5, HXT7 and GAL2, of which HXT7, HXT5 and GAL2 are most preferred (see Sedlack and Ho, Yeast 2004; 21: 671-684). Another preferred transporter for expression in yeast is the glucose transporter encoded by the P. stipitis SUT1 gene (Katahira et al., 2008, Enzyme Microb. Technol. 43: 115-119). Similarly orthologues of these transporter genes in other species may be overexpressed. Other genes that may be overexpressed in the cells of the invention include genes coding for glycolytic enzymes and/or ethanologenic enzymes such as alcohol dehydrogenases. Preferred endogenous genes for inactivation include hexose kinase genes e.g. the S. cerevisiae HXK2 gene (see Diderich et al., 2001, Appl. Environ. Microbiol. 67: 1587-1593); the S. cerevisiae MIG1 or MIG2 genes; genes coding for enzymes involved in glycerol metabolism such as the S. cerevisiae glycerol-phosphate dehydrogenase 1 and/or 2 genes; or (hybridising) orthologues of these genes in other species. Other preferred further modifications of host cells for xylose fermentation are described in van Maris et al. (2006, Antonie van Leeuwenhoek 90:391-418), WO2006/009434, WO2005/023998, WO2005/111214, and WO2005/091733. Any of the genetic modifications of the cells of the invention as described herein are, in as far as possible, preferably introduced or modified by self cloning genetic modification.
In a preferred transformed host cell according to the invention, the nucleic acid construct confers to the host cell the ability to grow on xylose as carbon/energy source, preferably as sole carbon/energy source, and preferably under anaerobic conditions, i.e. conditions as defined herein below for anaerobic fermentation process. Preferably, when grown on xylose as carbon/energy source the transformed host produces essentially no xylitol, e.g. the xylitol produced is below the detection limit or e.g. less than 5, 2, 1, 0.5, or 0.3% of the carbon consumed on a molar basis. Preferably, in case carbon/energy source also includes arabinose, the cell produces essentially no arabinitol, e.g. the arabinitol produced is below the detection limit or e.g. less than 5, 2, 1, 0.5, or 0.3% of the carbon consumed on a molar basis.
A transformed host cell of the invention preferably has the ability to grow on xylose as sole carbon/energy source at a rate of at least 0.01, 0.02, 0.05, 0.1, 0.2, 0.25 or 0.3 h−1 under aerobic conditions, or, more preferably, at a rate of at least 0.005, 0.01, 0.02, 0.05, 0.08, 0.1, 0.12, 0.15 or 0.2 h−1 under anaerobic conditions. A cell of the invention preferably has the ability to grow on a mixture of glucose and xylose (in a 1:1 weight ratio) as sole carbon/energy source at a rate of at least 0.01, 0.02, 0.05, 0.1, 0.2, 0.25 or 0.3 h−1 under aerobic conditions, or, more preferably, at a rate of at least 0.005, 0.01, 0.02, 0.05, 0.08, 0.1, 0.12, 0.15 or 0.2 h−1 under anaerobic conditions. Thus, in a preferred transformed host cell according to the invention, the nucleic acid construct confers to the host cell the ability to anaerobically ferment xylose as sole carbon source in a process wherein ultimately pyruvate is used as an electron (and hydrogen acceptor) and is reduced to fermentation products such as ethanol, lactic acid, 3-hydroxy-propionic acid, acrylic acid, acetic acid, succinic acid, citric acid, amino acids, 1,3-propane-diol, ethylene, glycerol, β-lactam antibiotics and cephalosporins.
Preferably, a cell of the invention has a specific xylose consumption rate of at least 200, 300, 400, 600, 700, 800, 900 or 1000 mg h−1 (g dry weight)−1. Preferably, a cell of the invention has a yield of fermentation product (such as ethanol) on xylose that is at least 20, 40, 50, 60, 80, 90, 95 or 98% of the cell's yield of fermentation product (such as ethanol) on glucose. More preferably, the modified host cell's yield of fermentation product (such as ethanol) on xylose is equal to the host cell's yield of fermentation product (such as ethanol) on glucose. Likewise, the modified host cell's biomass yield on xylose is preferably at least 55, 60, 70, 80, 85, 90, 95 or 98% of the host cell's biomass yield on glucose. More preferably, the modified host cell's biomass yield on xylose is equal to the host cell's biomass yield on glucose. It is understood that in the comparison of yields on glucose and xylose both yields are compared under aerobic conditions or both under anaerobic conditions.
In another aspect the invention relates to a process for producing a fermentation product selected from the group consisting of ethanol, lactic acid, 3-hydroxy-propionic acid, acrylic acid, acetic acid, succinic acid, citric acid, amino acids, 1,3-propane-diol, ethylene, glycerol, β-lactam antibiotics and cephalosporins. The process preferably comprises the steps of: a) fermenting a medium containing a source of xylose, and optionally arabinose, with a cell as defined hereinabove, whereby the cell ferments xylose, and optionally arabinose, to the fermentation product, and optionally, b) recovery of the fermentation product.
In addition to a source of xylose the carbon source in the fermentation medium may also comprise a source of glucose. The skilled person will further appreciate that the fermentation medium may further also comprise other types of carbohydrates such as e.g. in particular a source of arabinose. The sources of xylose, glucose and arabinose may be xylose, glucose and arabinose as such (i.e. as monomeric sugars) or they may be in the form of any carbohydrate oligo- or polymer comprising xylose, glucose and/or arabinose units, such as e.g. lignocellulose, arabinans, xylans, cellulose, starch and the like. For release of xylose, glucose and/or arabinose units from such carbohydrates, appropriate carbohydrases (such as arabinases, xylanases, glucanases, amylases, cellulases, glucanases and the like) may be added to the fermentation medium or may be produced by the modified host cell. In the latter case the modified host cell may be genetically engineered to produce and excrete such carbohydrases. An additional advantage of using oligo- or polymeric sources of glucose is that it enables to maintain a low(er) concentration of free glucose during the fermentation, e.g. by using rate-limiting amounts of the carbohydrases preferably during the fermentation. This, in turn, will prevent repression of systems required for metabolism and transport of non-glucose sugars such as xylose and arabinose. In a preferred process the modified host cell ferments both the xylose and glucose, and optionally arabinose, preferably simultaneously in which case preferably a modified host cell is used which is insensitive to glucose repression to prevent diauxic growth. In addition to a source of xylose (and glucose) as carbon source, the fermentation medium will further comprise the appropriate ingredient required for growth of the modified host cell. Compositions of fermentation media for growth of eukaryotic microorganisms such as yeasts and filamentous fungi are well known in the art.
The fermentation process may be an aerobic or an anaerobic fermentation process. An anaerobic fermentation process is herein defined as a fermentation process run in the absence of oxygen or in which substantially no oxygen is consumed, preferably less than 5, 2.5 or 1 mmol/L/h, more preferably 0 mmol/L/h is consumed (i.e. oxygen consumption is not detectable), and wherein organic molecules serve as both electron donor and electron acceptors. In the absence of oxygen, NADH produced in glycolysis and biomass formation, cannot be oxidised by oxidative phosphorylation. To solve this problem many microorganisms use pyruvate or one of its derivatives as an electron and hydrogen acceptor thereby regenerating NAD+. Thus, in a preferred anaerobic fermentation process pyruvate is used as an electron (and hydrogen acceptor) and is reduced to fermentation products such as ethanol, as well as non-ethanol fermentation products such as lactic acid, 3-hydroxy-propionic acid, acrylic acid, acetic acid, succinic acid, citric acid, amino acids, 1,3-propane-diol, ethylene, glycerol, butyric acid, caproate, butanol, glyoxylate, β-lactam antibiotics and cephalosporins. Anaerobic processes of the invention are preferred over aerobic processes because anaerobic processes do not require investments and energy for aeration and in addition, anaerobic processes produce higher product yields than aerobic processes. Alternatively, the fermentation process of the invention may be run under aerobic oxygen-limited conditions. Preferably, in an aerobic process under oxygen-limited conditions, the rate of oxygen consumption is at least 5.5, more preferably at least 6 and even more preferably at least 7 mmol/L/h.
The fermentation process is preferably run at a temperature that is optimal for the modified cells of the invention. Thus, for most yeasts or fungal cells, the fermentation process is performed at a temperature which is less than 42° C., preferably less than 38° C. For yeast or filamentous fungal cells, the fermentation process is preferably performed at a temperature which is lower than 35, 33, 30 or 28° C. and at a temperature which is higher than 20, 22, or 25° C.
Preferably in the fermentation processes of the invention, the cells stably maintain the nucleic acid constructs that confer to the cell the ability of isomerising xylose into xylulose, and optionally converting arabinose into D-xylulose 5-phosphate. Preferably in the process at least 10, 20, 50 or 75% of the cells retain the abilities of isomerising xylose into xylulose, and optionally converting arabinose into D-xylulose 5-phosphate after 50 generations of growth, preferably under industrial fermentation conditions.
A preferred fermentation process according to the invention is a process for the production of ethanol, whereby the process comprises the steps of: a) fermenting a medium containing a source of xylose, and optionally arabinose, with a cell as defined hereinabove, whereby the cell ferments xylose, and optionally arabinose, to ethanol, and optionally, b) recovery of the ethanol. The fermentation medium may further be performed as described above. In the process the volumetric ethanol productivity is preferably at least 0.5, 1.0, 1.5, 2.0, 2.5, 3.0, 5.0 or 10.0 g ethanol per liter per hour. The ethanol yield on xylose and/or glucose and/or arabinose in the process preferably is at least 50, 60, 70, 80, 90, 95 or 98%. The ethanol yield is herein defined as a percentage of the theoretical maximum yield, which, for xylose, glucose and arabinose is 0.51 g. ethanol per g. xylose, glucose or arabinose.
A further preferred fermentation process according to the invention is a process which comprises fermenting a medium containing a source of xylose and a source of arabinose wherein however two separate strains of cells are used, a first strain of cells as defined hereinabove except that cells of the first strain do not have the ability to converting arabinose into D-xylulose 5-phosphate, which cells of the first strain ferment xylose to the fermentation product; and a second strain of cells as defined hereinabove except that cells of the second strain do not have the ability to (directly) isomerise xylose to xylulose, which cells of the second strain ferment arabinose to the fermentation product. The process optionally comprises the step of recovery of the fermentation product. The cells of the first and second are further as otherwise described hereinabove.
In this document and in its claims, the verb “to comprise” and its conjugations is used in its non-limiting sense to mean that items following the word are included, but items not specifically mentioned are not excluded. In addition, reference to an element by the indefinite article “a” or “an” does not exclude the possibility that more than one of the element is present, unless the context clearly requires that there be one and only one of the elements. The indefinite article “a” or “an” thus usually means “at least one”.
All patent and literature references cited in the present specification are hereby incorporated by reference in their entirety.
The following examples are offered for illustrative purposes only, and are not intended to limit the scope of the present invention in any way.
1. Functional Expression of Xylose Isomerases of the Invention in Yeast
1.1 Host Organism
The yeast host strain was RN1000. This strain is a derivative of strain RWB 218 (Kuyper et al., FEMS Yeast Research 5, 2005, 399-409). The plasmid pAKX002 encoding the Piromyces XylA is lost in RN1000. The genotype of the host strain is: MatA, ura3-52, leu2-112, gre3::hphMX, loxP-Ptpi::TAL1, loxP-Ptpi::RKI1, pUGPtpi-TKL1, pUGPtpi-RPE1, {p415 Padh1XKS1Tcyc1-LEU2}.
1.2 Expression-Constructs with Synthetic XI Genes
Synthetic codon-optimised (for Saccharomyces cerevisiae) XI genes were cloned into a derivative of pRS306 (Sikorski R. S., Hieter P., 1989, “A system of shuttle vectors and yeast host strains designed for efficient manipulation of DNA in Saccharomyces cerevisiae” Genetics 122:19-27) comprising the Saccharomyces cerevisiae TPI1 promoter (899 bp) and the CYC1 terminator (288 bp) sequences, using XbaI (at the 5′-end of the synthetic genes) and BamHI (at the 3′-end of the synthetic genes) restriction sites. The first three nucleotides in front of the ATG were modified into AAA in order to optimize expression. Table 1 provides a list of the XI sequences that were tested and the corresponding SEQ ID NO's depicting the synthetic sequences. Genes were synthesized by GenScript Corporation (see www.genscript.com) and delivered cloned in pUC57 (GenBank Y14837.1). The TPI promoter was obtained using yeast genomic DNA as template in a PCR with primers:
forward: AAACCGGTTTCTTCTTCAGATTCCCTC (SEQ ID NO:31);
reverse: TTAGATCTCTAGATTTATGTATGTGTTTTTTGTAGT SEQ ID NO:32). The CYC1 terminator was obtained using yeast genomic DNA as template in a PCR with primers:
forward: AAGAATTCGGATCCCCTTTTCCTTTGTCGA (SEQ ID NO:33);
reverse: AACTCGAGCCTAGGAAGCCTTCGAGCGTC (SEQ ID NO:34).
1.3 Transformation of the Host Organism and Selection of Transformants
RN1000 was transformed with plasmids using the ‘Gietz method’ (Gietz et al., 1992, Nucleic Acids Res. 1992 Mar. 25; 20(6):1425). Primary selection of transformants was done on mineral medium (YNB+2% glucose) via uracil complementation.
1.4 Enzyme Assays
Xylose isomerase activity is assayed at 37° C. in a reaction mixture containing 50 mM phosphate buffer (pH 7.0), 10 mM xylose, 10 mM MgCl2 and a suitable amount of cell-free extract. One unit of activity is defined as the amount of enzyme producing 1 nmol of xylulose per min under the assay conditions. Xylulose formed is determined by the method of Dische and Borenfreund (Dische and Borenfreund, 1951, J. Biol. Chem. 192: 583-587) or by HPLC using a Biorad HPX-87N Column operated at 80° C. and eluated at 0.6 ml/min using 0.01 M Na2HPO4 as the eluens. Xylose and xylulose are detected by a Refractive Index detector at an internal temperature of 60° C.
Specific activity is expressed as units per mg protein. Protein is determined with the Bio-Rad protein reagent (Bio-Rad Laboratories, Richmond, Calif., USA) with bovine γ-globulin as a standard.
1.5 Physiological Characterisation of the Transformed Cells
Transformed cells were colony-purified on minimal medium with glucose as sole carbon source several times. Subsequently colony-purified transformed cells are grown in shake flasks in the presence of oxygen on synthetic medium with 2% (w/v) xylose as carbon/energy source. The results are shown in Table 2 where “+” indicates that cells showed significant growth. The sign “−” denotes that no significant growth occurred.
Strains growing at the expense of xylose were subsequently tested for their ability to grow anaerobically at the expense of xylose with a concomitant formation of ethanol. Strains transformed with the xylose isomerases of Cyllamyces aberensis, Ciona intestinalis, Clostridium difficile, Bacteroides fragilis and Fusobacterium mortiferum were able to grow anacrobically on xylose with growth rates, biomass and ethanol yields comparable to those of the prior art Piromyces enzyme, e.g. comparable to those of RWB218 as previously described by Kuyper et al. (2005, FEMS Yeast Res. 5: 925-934). However, cells transformed with the C. difficile XI showed the best performance in xylose fermentation in terms of growth rate.
Similarly the transformed cells of the invention are also capable of mixed substrate utilisation. When the transformed cells are grown in a mixture of glucose and xylose (20 g l−1 each) both sugars are completely consumed but glucose was the preferred substrate. Xylose consumption commences only after approximately 80% of the glucose is consumed. The ethanol produced accounted for the consumption of the total of glucose and xylose in each instance of the strains transformed with the xylose isomerases of Cyllamyces aberensis, Ciona intestinalis, Clostridium difficile, Bacteroides fragilis and Fusobacterium mortiferum.
Piromyces_sp_E2
Cyllamyces_aberensis
Clostridium_difficile
Bacteroides_fragilis
Ciona_intestinalis
Thermotoga_maritima
Haemophilus_somnus
Physcomitrella_patens
Arabidopsis_thaliana
Arthrobacter_aurescens
Burkholderia_phytofirmans
Orpinomyces_sp._Ukk1
Fusobacterium_mortiferum
Piromyces XI
Piromyces
Cyllamyces aberensis
Physcomitrella patens
Arabidopsis thaliana
Haemophilus somnus
Ciona intestinalis
Clostridium difficile
Thermatoga maritima
Bacteroides fragilis
Burkholderia phytofirmans
Arthrobacter aurescens
Piromyces_sp_E2
Bacteroides_fragilis
Cyllamyces_aberensis
Clostridium_difficile
Ciona_intestinalis
Fusobacterium_mortiferum
Orpinomyces_sp_ukk1
Clostridium_phytofermentans
Bacteroides_uniformis
Thermotoga_maritima
Haemophilus_somnus
Arabidopsis_thaliana
Physcomitrella_patens
Burkholderia_phytofirmans
Arthrobacter_aurescens
Arabidopsis thaliana
Physcomitrella patens
Ciona intestinalis
Piromyces sp E2
Orpinomyces sp ukk1
Cyllamyces aberensis
Bacteroides fragilis
Bacteroides uniformis
Clostridium difficile
Fusobacterium mortiferum
Thermotoga maritima
Clostridium phytofermentans
Haemophilus somnus
Burkholderia phytofirmans
Arthrobacter aurescens
Arabidopsis thaliana
Physcomitrella patens
Ciona intestinalis
Piromyces sp E2
Orpinomyces sp ukk1
Cyllamyces aberensis
Bacteroides fragilis
Bacteroides uniformis
Clostridium difficile
Fusobacterium mortiferum
Thermotoga maritima
Clostridium phytofermentans
Haemophilus somnus
Burkholderia phytofirmans
Arthrobacter aurescens
Arabidopsis thaliana
Physcomitrella patens
Ciona intestinalis
Piromyces sp E2
Orpinomyces sp ukk1
Cyllamyces aberensis
Bacteroides fragilis
Bacteroides uniformis
Clostridium difficile
Fusobacterium mortiferum
Thermotoga maritima
Clostridium phytofermentans
Haemophilus somnus
Burkholderia phytofirmans
Arthrobacter aurescens
Arabidopsis thaliana
Physcomitrella patens
Ciona intestinalis
Piromyces sp E2
Orpinomyces sp ukk1
Cyllamyces aberensis
Bacteroides fragilis
Bacteroides uniformis
Clostridium difficile
Fusobacterium mortiferum
Thermotoga maritima
Clostridium phytofermentans
Haemophilus somnus
Burkholderia phytofirmans
Arthrobacter aurescens
Arabidopsis thaliana
Physcomitrella patens
Ciona intestinalis
Piromyces sp E2
Orpinomyces sp ukk1
Cyllamyces aberensis
Bacteroides fragilis
Bacteroides uniformis
Clostridium difficile
Fusobacterium mortiferum
Thermotoga maritima
Clostridium phytofermentans
Haemophilus somnus
Burkholderia phytofirmans
Arthrobacter aurescens
Arabidopsis thaliana
Physcomitrella patens
Ciona intestinalis
Piromyces sp E2
Orpinomyces sp ukk1
Cyllamyces aberensis
Bacteroides fragilis
Bacteroides uniformis
Clostridium difficile
Fusobacterium mortiferum
Thermotoga maritima
Clostridium phytofermentans
Haemophilus somnus
Burkholderia phytofirmans
Arthrobacter aurescens
Arabidopsis thaliana
Physcomitrella patens
Ciona intestinalis
Piromyces sp E2
Orpinomyces sp ukk1
Cyllamyces aberensis
Bacteroides fragilis
Bacteroides uniformis
Clostridium difficile
Fusobacterium mortiferum
Thermotoga maritima
Clostridium phytofermentans
Haemophilus somnus
Burkholderia phytofirmans
Arthrobacter aurescens
Arabidopsis thaliana
Physcomitrella patens
Ciona intestinalis
Piromyces sp E2
Orpinomyces sp ukk1
Cyllamyces aberensis
Bacteroides fragilis
Bacteroides uniformis
Clostridium difficile
Fusobacterium mortiferum
Thermotoga maritima
Clostridium phytofermentans
Haemophilus somnus
Burkholderia phytofirmans
Arthrobacter aurescens
Arabidopsis thaliana
Physcomitrella patens
Ciona intestinalis
Piromyces sp E2
Orpinomyces sp ukk1
Cyllamyces aberensis
Bacteroides fragilis
Bacteroides uniformis
Clostridium difficile
Fusobacterium mortiferum
Thermotoga maritima
Clostridium phytofermentans
Haemophilus somnus
Burkholderia phytofirmans
Arthrobacter aurescens
| Number | Date | Country | Kind |
|---|---|---|---|
| 08172919 | Dec 2008 | EP | regional |
This application is a divisional of U.S. patent application Ser. No. 13/142,124, filed Sep. 13, 2011 (now U.S. Pat. No. 9,334,488), which claims priority from National Stage Entry of PCT/NL2009/050803, filed Dec. 24, 2009, and U.S. Provisional Patent Application No. 61/140,795, filed Dec. 24, 2008, the contents of which are incorporated herein by reference in their entireties.
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| Number | Date | Country | |
|---|---|---|---|
| 20160230162 A1 | Aug 2016 | US |
| Number | Date | Country | |
|---|---|---|---|
| 61140795 | Dec 2008 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 13142124 | US | |
| Child | 15093726 | US |
