Process for Producing Alcohol Using Yeast Transformed by Rhizopus Glucoamylase Gene

The present invention relates to a process for producing a glucoamylase and alcohol using a yeast which is engineered by recombinant DNA technology so as to acquire the ability to produce glucoamylase derived from Rhizopus oryzae.

Glucoamylase is an enzyme which hydrolyzes starch into glucose from the non-reducing terminal and, therefor is widely used for saccharifying starch in the production of ethanol from starchy materials

The glucoamylase derived from the genus Rhizopus is produced in particularly high productivity and high enzyme activity. Furthermore, in contrast to common glucoamylase, Rhizopus glucoamylase exhibits a strong action on raw starch and its enzymological and chemical properties including optimum pH are particularly suitable for the saccharification of cereal starch. Because of these features, the Rhizopus-derived glucoamylase is considered to be best suited to alcohol production by non-cooking or low-temperature cooking techniques (see U.S. Pat. Nos. 4,514,496 and 4,092,434).

However, Rhizopus glucoamylase is usually produced by cultivation on a solid medium using wheat bran as the principal substrate, and this increases the cost of enzyme production as compared with a liquid culture which can be carried out on a tank scale, and hence alcohol production using glucoamylase will be expensive.

The present inventors assumed that the above problem could be resolved if the glucoamylase gene of Rhizopus was incorporated into a host yeast so that it can be expressed. Such yeast can directly utilize starch including low temperature cooked starchy materials and non-cooked starchy materials, thereby reducing the cost of ethanol production in the process of producing said alcohol from starch by saving or even avoiding the use of Rhizopus glucoamylase preparation for saccharifying starch. The inventors conducted extensive research on the basis of the above assumption in order to complete the present invention.

FIGS. 1a-c show the nucleotide sequence of the intron-free glucoamylase structural gene of the invention together with the signal peptide region;

FIGS. 2a-d show the nucleotide sequence of a glucoamylase gene cloned from the chromosomal DNA or Rhizopus oryzae;

FIG. 3a-b show the nucleotide sequence of the C-terminal region of a glucoamylase gene cloned from the cDNA obtained from the mRNA of Rhizopus oryzae;

FIG. 4 compares the glucoamylase gene cloned from the chromosomal DNA of Rhizopus oryzae with the glucoamylase gene prepared from the mRNA of Rhizopus oryzae;

FIGS. 5, 6A, 6B and 6C are flowsheets showing the steps for constructing, in a plasmid vector, an intron-free cDNA of the complete length by combining the two genes shown in FIG. 4, and for incorporating a promoter and a tail with a view to ensuring efficient gene expression in yeast, wherein FIG. 5 shows the steps for producing pCGA469, FIG. 6A illustrates the steps for producing pYGA2149 and pYGA2169, and FIG. 6B depicts the steps for producing pYGIFLm222;

FIG. 7 is a graph showing the profile of glucoamylase production using transformed yeasts as performed in Example 1;

FIG. 8 is an electrophoretic diagram for glucoamylase samples produced by transformed yeasts in Example 1;

FIG. 9 is a graph showing growth curves for transformed yeasts that were cultured in Example 1 using starch as a sole carbon source;

FIG. 10 is a graph showing the profile of alcohol production by one of the transformed yeasts prepared in Example 1; and

FIG. 11 is a graph showing the production of glucoamylase by the transformed yeasts obtained in Example 2.

The present invention relates to a process for producing ethanol, wherein a glucoamylase gene derived from a filamentous fungus of the genus Rhizopus is incorporated into a recombinant vector in a manner capable of being expressed, which is then used to transform a yeast host for saccharifying starchy material to facilitate fermentation.

The starchy materials employable in the process of the invention include, for example, cereals, subterranean starches such as cassava, sweet potato, potato, as well as pure starch.

In order to produce the Rhizopus glucoamylase by a microorganism in accordance with the method of the invention, the glucoamylase gene can be prepared by an appropriate method from a filamentous fungus of the genus Rhizopus capable of producing glucoamylase, preferably Rhizopus oryzae; incorporating said gene into a plasmid vector capable of replicating in a host cell together with a DNA fragment comprising an expression mechanism of information such as a promoter region and a tail region which is recognized in an expression system of the host; and the host is then transformed by said vector. If yeast is used as a host, the transformed yeast produces and secretes Rhizopus glucoamylase which saccharifies any starch including non-cooked starch and hence the yeast host will convert the resulting glucose into alcohol. Thus alcohol can be produced without the addition of an expensive saccharifying enzyme from outside. It has not previously been known that alcohol may be produced by direct action of yeast on starch without previous saccharification of the starch.

The high temperature cooking process (cooked at above 120.degree. C.), the low temperature cooking process (cooked at 60.degree.-85.degree. C.), and the non-cooking process are known steps for cooking or gelatinizing the raw material before saccharification in the production of alcohol. Any of the above processes may be employed in the alcohol production of the present invention.

Instead of simultaneously producing alcohol and Rhizopus glucoamylase in a yeast host, bacterial cells of Bacillus subtilis may be used as a host if Rhizopus glucoamylase is the only desired product.

According to the present invention, a method for obtaining DNA encoding the glucoamylase and the novel information of the nucleotide sequence of said DNA are also provided.

The nucleotide sequence of the DNA fragment for the production of the glucoamylase in accordance with the process of the invention can be prepared by, for example, appropriately conjugating a part of the glucoamylase nucleotide sequence cloned from chromosomal DNA of Rhizopus oryzae and a part of the glucoamylase cDNA sequence prepared from mRNA of Rhizopus oryzae as described later in more detail. To use the glucoamylase gene thus prepared for expression in yeast, the gene is preferably combined with a promoter region and/or a tail region (3' non translational region) which are suitable for transformation of the host organism (see Unexamined Published Japanese Patent Application No. 146281/1983). For example, in order to have the glucoamylase gene expressed in a yeast, the promoter region (P.sub.GAP) and tail region (T.sub.GAP) of the glyceraldehyde-3-phosphate dehydrogenase gene (GAP-DH), the promoter region (Ppho5) of the acid phosphatase gene (PH05), and the promoter region (P.sub.PGK) of the 3-phosphoglycerokinase (PGK) may be employed as shown in Examples 1 and 2. A plasmid vector comprising these promoter and/or tail regions together with the gene of the present invention, as well as a microorganism transformed by such vector are preferred embodiments of the present invention.

Any fungi of the genus Rhizopus that are capable of producing glucoamylase may be used in the present invention for obtaining the desired gene. Illustrative species include Rhizopus oryzae, Rhizopus formosaensis, Rhizopus javanicus and Rhizopus thailandensis. The present inventors have confirmed that Rhizopus oryzae SAM 0034 (accession numbers FERM P-7960; FERM BP-929deposited at the Fermentation Research Institute (FRI), Agency of Industrial Science and Technology, Minestry of International Trade and Industry, Japan) produces a glucoamylase particularly suitable for hydrolyzing raw starch.

The present strain (SAM 0034) has the following mycological properties.

Colonies on Potato dextrose agar medium attain a diameter of 5-5.5 mm in one day at 28.degree. C. and cover 90 mm petri plates of Potato dextrose agar medium in two days, the colonies are white.

Colonies become grey with age.

Stolons are hyaline or yellowish brown; rhizoids brown. Sporangiophores usually arising from rhizoids, occasionally arising directly from stolons, either single or in groups, occasionally divided, 220-1200 .mu.m long. Sporangia are globose subglobose, dark brown, 60-150 .mu.m in diameter; columellae globose or subglobose. Sporangiospores are globose, subglobose, or angular, striatae on the surface, 5-15.times.3-7 .mu.m. Chlamydospores subglobose or cylindrical, 6-13.times.4-19 .mu.m.

No zygospores were observed.

At 37.degree. C., growth occurs.

The present strain (SAM 0034) can be accommodated in the fungus genus Rhizopus, because: (1) The sporangiospores are produced within the columellate sporangium; (2) The sporangiospores are brown; (3) the rhizoids are produced.

The mycological properties of the present strain (SAM 0034) are compared with those of known species of the genus Rhizopus, referring to Inui, T., Y. Takeda & H. Iizuka, 1965, Taxonomical Studies on genus Rhizopus (Journal of General and Applied Microbiology, Vol. 11, Supplement, 121 pp. Zycha, H., R. Siepmann & G. Linnemann, 1969, Mucorales. Eine Beschreibung aller Gattungen und Arten dieser Pilzgruppe, 335 pp., J. Cramer, Lehre. Domsch, K. H., W. Gams and T. -H. Anderson, 1980, Compendium of Soil Fungi. Vol. 1, 859 pp., Academic Press. London). The result of this comparison revealed that the present strain could be identified as Rhizopus oryzae, because: (1) The present strain can grow at 37.degree. C.; (2) The sporangiospores are striate and measure 5-15.times.3-7 .mu.m; (3) The sporangiophores measure 220-1200 .mu.m in length; (4) The sporangia measure 60-150 .mu.m in diameter.

Cloning of glucoamylase gene

The glucoamylase gene may be isolated in the form of cDNA prepared from the mRNA of Rhizopus or by cloning from the chromosomal DNA of Rhizopus using a synthetic origonucleotide corresponding to a part of amino acid sequence of Rhizopus glucoamylase.

Usually it is not easy to obtain the complete glucoamylase gene by the former method, while the gene obtained by the latter method usually contains intron sequences and thus cannot be expressed in host E. coli or yeast. In order to obtain a glucoamylase gene capable of expression in these hosts, an appropriate part of the cDNA from mRNA may be conjugated with the intron-free part of the DNA sequence of the chromosomal gene. If one or both DNA fractions lack suitable sites to be cleaved by restriction enzymes, a technique of in vitro mutagenesis may be employed to introduce suitable cleavage sites for conjugation purposes.

The glucoamylase gene used in the present invention involves not only the same nucleotide sequence coding for the bracketed amino acid sequence in FIG. 1a-c but also a nucleotide sequence corresponding to an amino acid sequence having an enzymatic activity comparable to that of the bracketed amino acids.

The Rhizopus-derived glucoamylase structural gene is a DNA fragment encoding the sequence of 26-604 amino acids from the N-terminal in FIG. 1a-c, or it corresponds to nucleotide sequence numbers 190-1926 designated in FIG. 1a-c. The region of 1-25 amino acids from the N-terminal is a signal peptide coding region involved in the extracellular secretion of glucoamylase from the host cell. When, as described below, glucoamylase was produced by a yeast using this signal peptide coding region, more than 90% of the glucoamylase produced was secreted in the culture medium. The secreted glucomaylase was purified by a routine method and the amino acid sequence at the N-terminus was examined; the amino acid sequence of the glucoamylase started at the 26th amino acid of the sequence given in FIG. 1a-c and this indicates that the region defined by 1-25 amino acids from the N-terminus will function as a signal peptide in the yeast as well.

A method that can be used with advantage for the purpose of isolating the glucoamylase gene shown above is described hereunder. The whole DNA is separated from a glucoamylase-producing fungus of the genus Rhizopus by a modified version of the method of Cryer et al. The microorganism is first sporulated and the spores produced are collected. The chromosomal DNA can be prepared from the fungal spores by first disrupting them with glass balls as described below in Example 1 (a-i). The mixture is then extracted by the method of Cryer et al. (Methods in cell Biology, 12:39-44 (1975)) and the extract is finally subjected to gel filtration. The resulting DNA fraction is digested with HindIII and cloned to the HindIII site of a known vector pBR322 to obtain a Rhizopus gene library in E. coli. The library may be recovered in the form of an ampicillin-resistant transformant.

A probe (DNA oligomer) described in Examples 1 and 2 for detecting glucoamylase gene is prepared and used in colony hybridization. Colonies that will hybridize with the probe are grown and the plasmid DNA is extracted.

The present invention is hereunder described in greater detail with reference to the following examples.

(a-i) DNA preparation and its cloning

The whole DNA was isolated from glucoamylase-producing Rhizopus oryzae. DNA isolation was performed by a modified version of the method of Cryer et al. that was described in Method in Cell Biology, vol. 12, pp. 39-44, 1975 and originally employed with yeasts. A thin potato slice was sterilized in an autoclave and the cells of Rhizopus oryzae were grown for sporulation. The spores produced were collected, suspended in a solution of 0.15M NaCl and 0.05M EDTA, and disrupted by treatment for 15 seconds in a Dyno mill using glass balls. Subsequent procedures were the same as those employed in the method of Cryer et al., except that in the last step, gel filtration using Biogel A.sub.5m (the tradename of Bio-Rad for a molecular sieve) was performed to isolate the whole DNA. This DNA fraction was digested with HindIII and cloned to the HindIII site of pBR322 to obtain a Rhizopus gene library in E. coli strain WA802. The strain was transformed by a routine method. The library was obtained as an ampicillin-resistant transformant.

(a-ii) Selection of transformant and characterization of the glucoamylase gene

Transformant selection was made by a method generally referred to as colony hybridization, using a nitrocellulose filter paper. The first step starts with the preparation of a probe for detecting the glucoamylase DNA. For this purpose, the purified Rhizopus glucoamylase was decomposed by a variety of proteases and the resulting peptides were separated and purified. These peptides were subjected to amino acid analysis and the primary structures were determined by routine methods. As a result, an amino acid sequence having the partial structure of Asp--Leu--Thr--Trp--Ser--His--Ala--Ser was obtained. It was also found that this glucoamylase had an N-terminal amino acid sequence of Ala--Ser--Ile--Pro and a C-terminal sequence of Ala--Ala. In order to prepare the desired probe, 32 different synthetic DNA oligomers each consisting of 14 bases (5'-ACNTGGTCNCAQGC-3') were produced by the triester solid-phase method from the amino acid sequence of Thr--Trp--Ser--His--Ala which was part of the sequence identified above and wherein N is an arbitrary base and Q is T or C from pyrimidine. These DNA oligomers were labelled with [.gamma.-.sup.32 p] ATP and T4-polynucelotidyl kinase and used as probes for detecting the glucoamylase gene. Transformed E. coli colonies that hybridized with these probes by colony hybridization were grown and plasmid DNAs were extracted. The extract was treated with restriction enzymes and the resulting DNA fragments were analyzed by agarose-gel electrophoresis. As for the colonies that hybridized with the probes, the DNA fragment inserted in the plasmid had a size of 4.3 kb, as well as one cleavage site each of BamHI, KpnI, MluI and SacI, two sites for DraI and three sites for BglII, but had no cleavage sites for AccI, BalI, ClaI, EcoRI, HpaI, PstI, PvuII, ScaI or XhoI. The plasmid having this DNA fragment was named pRGA39.

(b-i) RNA preparation and cDNA cloning

The whole RNA was isolated from the aerial hyphae of Rhizopus oryzae. For this purpose, known procedures including the use of guanidium thiocyanate were followed. Polyadenylated RNA was recovered from the whole RNA as a mRNA fraction by way of chromatography on oligo-dT cellulose. Using this mRNA, a cDNA gene library was formed in E. coli WA802 by the method of Okayama and Berg described in Okayama, H. & Berg, P., Mol Cell Biol., 2, 161, 1982.

(b-ii) Transformant selection and characterization of glucoamylase cDNA

Selection of the transformant having the c-DNA of the glucoamylase was made by the aforementioned method of colony hybridization. A DraI fragment (2.0 kb) of the glucoamylase gene obtained in (a-ii) was used as a probe for detecting the glucoamylase cDNA. For this purpose, this fragment was labelled by the technique of nick translation using [.alpha.-.sup.32 P]dCTP, DNA polymerase I and DNase I. The transformed colonies that would hybridize with this probe were allowed to grow and the plasmid DNA was extracted. The extract was treated with restriction enzymes and the resulting DNA fragments were analyzed by electrophoresis on agarose gel. The DNA fragment which had been inserted into the plasmid of the colonies that hybridized with the probe had a size of 1.7 kb. This plasmid was named pCGA239.

(c) Nucleotide DNA sequence analysis

Plasmids pRGA39 and pCGA239 were digested with restriction enzymes and DNA fragments were isolated on agarose gel. Their nucleotide sequences were determined by the dideoxy method using recombinant phage M13. Analysis of pRGA39 revealed that this gene contained four introns each having a length of several tens of bp (for the intron sites, see FIG. 2a-d. The plasmid pCGA239 was not a cDNA corresponding to the full length of glucoamylase but lacked about 50 amino acids. Restriction maps of pRGA39 and pCGA239 are compared in FIG. 4.

(d) Construction of glucoamylase gene to be expressed

The cloned cDNA did not have the full length. A cDNA of the full length having in addition a glucoamylase promoter (derived from Rhizopus) was prepared by conjugating appropriate parts of pCGA239 and pRGA39. Since suitable restriction sites available for conjugation purposes were absent from the plasmids, the SalI site was introduced at the corresponding locations of pCGA239 and pRGA39 by the method of in vitro mutagenesis before performing the conjugation (see FIG. 5). For the method of in vitro mutagenesis, see Morinaga, Y. et al., BIO/THCHNOLOGY, 2, 636-639 (1984).

Because of the introduction of the SalI site, the 53rd amino acid codon from the N terminal of the treated plasmid PCGA439 was aspartic acid rather than lysine which was initially present. Therefore, the plasmid was again subjected to in vitro mutagenesis, whereby plasmid pCGA449 (deposited in the TRJ under accession number FERM BP-673) containing glucoamylase DNA of the full length having the inherent nucleotide sequence was obtained. This plasmid has been deposited with the Fermentation Research Institute, the Agency of Industrial Science and Technology, under designation of SAM0039 in accordance with the Budapest Treaty and has been assigned accession number FERM BP-673.

The full-length glucoamylase gene in pCGA449 is the combination of the sequence appearing before the arrow in FIG. 2(a) and the sequence appearing after the arrow in FIG. 3.

(e) Construction of expression vector in yeast

(e-i) With a view to ensuring efficient expression of pCGA449 in a yeast, a fragment (ca. 8.3 kb) cut out with EcoRI-SalI from pYGIFLm212 (FRI accession number FERM BP-2216; converted from FERM P-7727) having the acid phosphatase promoter (Ppho5) disclosed in Japanese Patent Application No. 157037/1984 was used. The promoter Ppho5 is also contained in the plasmid deposited at FRI under accession number FERM BP-383. In order to incorporate pCGA449 at the EcoRI-SalI site, the PvuII site of pCGA449 was converted to XhoI site with XhoI linker, whereby plasmid pCGA450 was prepared (FIG. 6A). This plasmid was cleaved with XhoI and EcoRI and a 2.2 kb fragment was separated by agarose gel electrophoresis. This fragment was ligated to the previously obtained 8.3 kb EcoRI-SalI fragment with a T4-DNA ligase. The resulting plasmid containing Ppho5 as a promoter was named pYGA2149. This plasmid was grown in E. coli strain WA802 and then separated (see FIG. 6A). (e-ii) With a view to ensuring efficient expression of pCGA469 in a yeast, a fragment (ca. 8.9 kb) cut out with EcoRI-SalI from pYGIFLm222 having the glyceraldehyde-3-phosphate dehydrogenase promoter (P.sub.GAP) disclosed in Japanese Patent Application No. 184291/1982 was used. In order to incorporate pCGA469 at the EcoRI-SalI site, the PvuII site of pCGA469 was converted to an XhoI site with a XhoI linker, whereby plasmid pCGA470 was prepared (FIG. 6C). This plasmid was cleaved with XhoI and EcoRI and a 2.2 kb fragment was separated by agarose gel electrophoresis. This fragment was ligated to the previously obtained 8.9 kb EcoRI-SalI fragment with a T4-DNA ligase. The resulting plasmid containing P.sub.GAP as a promoter was named pYGA 2269. This plasmid was grown in E. coli strain WA802 and then separated (see FIG. 6C). The plasmid pYGIFLm222 used above was prepared (FIG. 6B) by replacing the expression promoter Ppho5 in pYGIFLm212 with a glyceraldehyde-3-phosphate dehydrogenase promoter (P.sub.GAP see Japanese Patent Application No. 184291/1982). Detailed procedures were as follows: the unique BamHI site in pYGIFLm212 was cleaved with BamHI, filled in with DNA polymerase I, and treated with a HindIII linker to convert the BamHI site to a HindIII site, whereby plasmid pYGIFLm212H was obtained. Using the technique of in vitro mutagenesis, an EcoRI site was introduced into pYgap87 (deposited in the FRI under accession number FERM BP-382) immediately upstream from ATG (the initiation codon for the replication of the structural gene of glyceraldehyde-3-phosphate dehydrogenase), whereby plasmid pYgap87E was prepared. The plasmid pYGIFLm212H was cleaved with EcoRI, further cleaved partially with HindIII and then subjected to agarose gel electrophoresis to isolate an 8.0 kb fragment. The plasmid pYgap87E was cut with EcoRI and HindIII and subjected to agarose gel electrophoresis to isolate a 1.1 kb fragment. This fragment was ligated with the foregoing 8.0 kb fragment of pYGIFLm212H and the resulting recombinant plasmid pYGIFLm222 was recovered from the transformed E. coli.

pYGA2169 was prepared from pYGIFLm212 using pCGA469 and repeating the same procedures as described above and the plasmid was separated (FIG. 6A).

pYGA2249 (not shown) was also prepared by the same procedures as described above and separated. (f) Expression of the glucoamylase gene in yeast

The plasmid pYGA2149 was used to transform yeast [Saccharomyces cerevisiae strains XS-30-2A (MAT.alpha., leu2, his3, trpl, ura3) and XS-30-2B (MAT.alpha., leu2, his3, trpl, ura3)]and the transformed colonies were selected on the basis of the nutrient requirement for tryptophan as a marker. Transformation was performed by the method of Ito et al. (Ito, H. et al., J. Bacteriol., 153, 1983) using LiCl. A platinum loopful of the transformed colonies were inoculated in 5 ml of YPD medium (1% yeast extract, 2% polypeptone and 2% glucose) and sampling was made 48 hours later. Centrifugation (10,000 rpm.times.5 min) was conducted in an Eppendorf tube thus separating the sample into the supernatant and pellet. The activity of glucoamylase in the supernatant was measured by the following procedures: 200 .infin.l of the supernatant was added to 800 .mu.l of a soluble starch solution (1.0% soluble starch in 20 mM acetate buffer solution, pH 5.0) and the mixture was left to stand at 37.degree. C. The amount of released glucose was determined with a glucostat (Fujisawa Pharmaceutical Co., Ltd.). The activity data for the 2-hour reaction were as follows: 0.004 U/ml for pYGA2149 in XS-30-2A and 0.008 U/ml in XS-30-2B, indicating the sex-dependent difference by a factor of 2 (see FIG. 7). Activity of one unit (U) corresponds to 1 .mu.mol of glucose released in 1 minute. No activity was observed in the supernatants obtained from yeast which did not contain pYGA2149.

The glucoamylase activity for the plasmid using P.sub.GAP as a promoter was 0.40 U/ml, which was 50-100 times the value for the case where such promoter was absent. The glucoamylase activity for the plasmid using the acid phosphatase gene promoter Ppho5 was dependent on the phosphate concentration of the medium. For example, no glucoamylase activity was observed after 48-hour cultivation in the ordinary YPD medium at 30.degree. C., but an activity comparable to that for the use of P.sub.GAP appeared when the medium was replaced with YPD medium freed of phosphate by treatment with magnesium sulfate and ammonia water (Rubin, G. M., Eur. J. Biochem., 41, 197.times.202, 1974). The supernatant from the culture was subjected to SDS-polyacrylamide gel electrophoresis and no less than 50% of the total extracellular protein was glucoamylase protein.

It was confirmed by the following immunological techniques that the activities listed above were due to the Rhizopus-derived glucoamylase. A rabbit antibody was prepared using a purified glucoamylase. This antibody was used in the analysis by a method commonly referred to as Western blotting, using a concentrate of 1.5 ml of the same supernatant from the 48-hour culture that was employed in the previous activity measurements. One third portion of the concentrate was subjected to 10% polyacrylamide electrophoresis and the protein in the gel was transferred and immobilized on a nitrocellulose filter paper electrophoretically. The glucoamylase on the nitrocellulose filter paper was then detected by the known technique in enzyme immunology using the reaction with peroxidase. A band that would react with the glucoamylase antibody emerged at a position substantially equal to the Rhizopus glucoamylase in terms of molecular weight. This fact did indicate the expression of the Rhizopus-derived glucoamylase in yeasts. The data showing this fact are give in FIG. 8.

(g) Growth of yeast using starch as a sole carbon source

The effect of pYGA2149 on the growth of yeast strain XS-30-2B was investigated using different carbon sources. First, XS-30-2B was shake-cultured in YPD medium for 24 hours at 30.degree. C. and XS-30-2B (pYGA2149) was shake-cultured under the same conditions in a minimum nutrient medium (0.67% Difco Yeast nitrogen base and 2% glucose) containing 1% Casamino acids and uracil. A 100-ml portion each of YED medium or YPS medium (1% yeast extract, 2% polypeptone and 2% soluble starch) was added in a 500-ml Sakaguchi flask and sterilized in an autoclave. Each of the pre-culture suspensions (1 ml) was added to these mediums at 30.degree. C. and the subsequent growth was evaluated in terms of absorbance at 660 nm. The strain XS-30-2B harboring no plasmid pYGA2149 was capable of little growth in the YPS medium, but the strain harboring pYGA2149 grew at equal rates on both YPS and YED mediums. This fact clearly shows that XS-30-2B (pYGA2149) produced glucoamylase and utilized the starch hydrolyzed by the enzyme (see FIG. 9).

(h) Alcohol production by transformed yeasts

(h-i) Alcohol fermentation with soluble starch

The medium used in this experiment was prepared by autoclaving (121.degree. C., 15 minutes) 200 ml of YPS medium (1% yeast extract, 2% polypeptone, and 1, 2 or 5% soluble starch) in a 500-ml Erlenmeyer flask. The following yeast strains were employed.

(1) XS-30-2B (control having no glucoamylase gene);

(2) XS-30-2B (transformed by pYGA2149) having a Rhizopus promoter;

(3) XS-30-2B (transformed by pYGA2169) having the promoter Ppho5; and

(4) XS-30-2B (transformed by pYGA2269) having the promoter P.sub.GAP.

Starting pre-culture was prepared by inoculating a platinum loopful of the yeast in a minimum nutrient medium (5 ml) containing 1% Casamino acids, uracil and adenine and shake-culturing at 28.degree. C. for 20 hours. This starting preculture was inoculated in a YPD medium in an amount of two percent and subjected to stationary cultivation at 28.degree. C. for 24 hours to obtain a final pre-culture. The final preculture was inoculated in YPS medium at five percent and subjected to stationary cultivation at 28.degree. C. for the purpose of investigating ethanol production. The cultivation of yeast strain (3) on and after the final pre-culture was conducted in a low phosphate YPD or YPS medium respectively with a view to inducing Ppho5. The same experiment was conducted for three different starch concentrations (1, 2 and 5%). The results of ethanol production and yeast growth are shown in Tables 1 and 2.

(h-ii) Alcohol fermentation with low-temperature cooked starch

Ground corn (140 g) was added to 402 ml of water, and after adding 0.5 g of .alpha.-amylase preparation (Termamil) as a viscosity reducer and 160 ppm of potassium metabisulfite as a germicide, the mixture was held at 80.degree.-82.degree. C. for 5 minutes, and then rapidly cooled.

Starting and final pre-cultures were prepared using the same strain as employed in (h-i) and the final pre-culture was added to the low-temperature cooked starch and the mixture was cultured at 28.degree. C. under three different conditions, i.e., in the absence of any additional component, in the presence of Casamino acids, uracil and adenine, and in the presence of Casamino acids, uracil, adenine and 0.4% glucose. The progress of fermentation (as evaluated in terms of the decrease in CO.sub.2) and alcohol production were investigated. A non-transformed yeast using the routine amount of Rhizopus glucoamylase was employed as a positive control. The results are shown in Tables 3 and 4 and in FIG. 10, from which one can see that the yeasts obtained in accordance with the present invention were capable of direct alcohol production from non-cooked or low-temperature cooked (LTC) starch without addition of a Rhizopus glucoamylase preparation.

(a) A 2.0 kb DNA fragment containing glucoamylase gene from pYGA2269 prepared in Example 1(e) was inserted into the HindIII site of a known vector YCp19, whereby pYGA195 was obtained (FIG. 6C). This plasmid, containing a centromere was present in yeast with a copy number of 1.

(b) Expression of glucoamylase gene in yeast

The plasmids, pYGA2269 and pYGA195, were used to transform yeast strain XS-30-2B (MAT.alpha., Leu2, his3, trpl, ura3) and the transformed colonies were selected by the nutrient requirement for tryptophan as a marker. Transformation was conducted by the method of Ito et al (ibid) using LiCl. The selected transformed colonies were cultured overnight at 30.degree. C. in 5 ml of a minimum nutrient medium (0.67% Yeast Nitrogen base, 2% glucose, 0.001% uracil, 0.0054% adenine, 0.0026% leucine and 0.0038% histidine). The culture solution was inoculated at one percent in 400 ml of the minimum nutrient medium in an Erlenmeyer flask (1,000 ml) and shake-cultured at 30.degree. C.

Sampling was conducted at approximate intervals of 3 hours, and the absorbance at 660 nm and the glucoamylase activity values at 24 and 48 hours were determined, by measuring the amount of free glucose that was released by reaction at 37.degree. C. of a mixture of the supernatant of the culture (50 .mu.l ) and 950 .mu.l of a soluble starch solution (0.5% soluble starch in 20 mM acetate buffer, pH 4.5). The amount of glucose was determined by a glucostat of Fujisawa Pharmaceutical Co., Ltd. One unit (U) of glucoamylase activity corresponds to 1 .mu.mole of glucose released in 1 minute. The yeasts transformed by pYGA2269 and pYGA195 produced glucoamylase activities in amounts of 0.2 U/ml and 0.5 U/ml, respectively, at 48 hours (see FIG. 11). This enzyme can be secreted in an adequate amount even from a plasmid with a copy number of 1 by expressing it in the presence of a strong promoter such as GAPDH promoter.

(c) Purification of the enzyme obtained by the recombinant DNA technology

S. cerevisiae XS-30-2B transformed by pYGA2269 was cultured for 3 days at 30.degree. C. in a medium containing 0.67% Yeast Nitrogen base, 2% Casamino acids, 2% glucose, 0.001% uracil, 0.0054% adenine, 0.0026% leucine and 0.0038% histidine. The supernatant of the culture was concentrated about 20-folds by an Amicon concentrator, dialyzed against an acetate buffer (20 mM CH.sub.3 COONa, pH 4.6), and adsorbed on an SP-Sephadex C-50 column equilibrated with the same buffer. A linear gradient from 0 to 200 mmol was applied to the column, whereby the active fractions eluted were recovered, dialyzed against water, freeze-dried and stored for the following experiments.

(d) Properties of enzymes produced by the recombinant yeast was in good agreement with the Gluc 1 having the highest molecular weight of the three glucoamylase molecules produced by the Rhizopus; the N-terminal sequence and isoelectric point of the glucoamylase were also the same as those of the Rhizopus-produced glucoamylase. The apparent molecular weight of the glucoamylase as determined by SDS-polyacrylamide electrophoresis was slightly higher than that of Gluc 1. The molecular weight of the glucomaylase was decreased by digestion with endoglycosidase H capable of cutting a certain sugar chain attached to the asparagine residue. However, the Rhizopus-produced glucoamylase is not sensitive to the action of endoglycosidase H. The difference between the two glucoamylase molecules with respect to the molecular weight would be ascribable to the differences in the amount and mode of sugar chain attachment.

No difference was observed with respect to pH dependency, heat stability or other parameters such as Vmax and Km for soluble starch. The Rhizopus-produced glucoamylase had an r/s value (r: activity on raw starch, s: activity on gelatinized soluble starch) of 0.47 while the value for the recombinant yeast produced glucoamylase was 0.56. It is therefore concluded that as far as the ability to decompose raw starch is concerned, a better glucoamylase preparation can be produced from the recombinant yeast, rather than from the Rhizopus.

(e) Adsorption site on starch

The Rhizopus-produced glucoamylase contains three molecules having different molecular weights, Gluc 1, 2 and 3, the last two of which would be the product of limited proteolysis of the N-terminal amino acid sequence of Gluc 1.

The behavior of these three molecules in adsorption to starch was investigated. A sample of enzyme solution was mixed with an equal volume of raw starch and, after leaving the mixture to stand in iced water for 30 minutes, it was subjected to centrifugation. The supernatant was recovered as a fraction of the enzyme which was not adsorbed on the starch while the precipitate was recovered as a fraction which was adsorbed on starch. Both fractions were analyzed by SDS-PAGE; Gluc 1 and the recombinant yeast produced glucoamylase were found in the precipitate whereas Gluc 2 and 3 were found in the supernatant. The mixture of Gluc 2 and 3 had an r/s value of 0.23, indicating that the Rhizopus glucomaylase lost its ability to be adsorbed onto raw starch by becoming deficient of the N-terminal sequence. It is therefore concluded that the N-terminal portion has a site which is adsorbed on raw starch. The Rhizopus glucoamylase was capable of hydrolysing gelatinized soluble starch as effectively as the glucoamylase of the full length even if it lost the N-terminal portion. When a mixture of glucoamylase solution with gelatinized soluble starch was subjected to column chromatography on Ultrogel AcA 44, both Gluc 1 and the recombinant yeast produced glucomaylase were eluted in the void volumes in the column together with the starch, but neither Gluc 2 nor 3 was adsorbed on the starch and they were eluted in the corresponding elution volumes. This provided a basis for the conclusion that Gluc 1 and the recombinant yeast produced glucoamylase are capable of adsorption not only on raw starch but also on gelatinized starch.