The present invention provides a novel lipase with a molecular weight of about 32 kDa, which is produced by a strain belonging to the genus Tetrasphaera , as well as a gene encoding the same. This lipase has the ability to recognize a medium-chain fatty acid as a substrate. The present invention also provides a novel lipase with a molecular weight of about 40 kDa, which is produced by a strain belonging to the genus Tetrasphaera and has the ability to recognize both a medium-chain fatty acid and a long-chain fatty acid as substrates, as well as a polynucleotide encoding the same. The present invention further provides Tetrasphaera sp. strain NITE P-154. The lipase of the present invention can be used as an immobilized enzyme and is useful in fields such as production of digestants and/or flavorings, production of clinical laboratory reagents, detergent enzymes and/or fats, as well as production of optically active intermediates for agricultural chemicals and pharmaceutical preparations.
1. An isolated polynucleotide comprising (A 1 ), (B 1 ), (C 1 ), (D 1 ), (E 1 ), (F 1 ) or (G 1 ) shown below:
(A 1 ) an isolated polynucleotide which consists of all of the nucleotide sequence shown in SEQ ID NO: 10 or a part thereof covering at least nucleotides 25-801;
(B 1 ) an isolated polynucleotide which is hybridizable under stringent conditions with a polynucleotide consisting of a nucleotide sequence complementary to the nucleotide sequence of the polynucleotide shown in (A 1 ) and which encodes a protein having lipase activity;
(C 1 ) an isolated polynucleotide which consists of a nucleotide sequence comprising substitution, deletion, insertion and/or addition of 1 to 9 nucleotides in the nucleotide sequence of the polynucleotide shown in (A 1 ) and which encodes a protein having lipase activity;
(D 1 ) an isolated polynucleotide which shares an identity of at least 80% or more with the nucleotide sequence of the polynucleotide shown in (A 1 ) and which encodes a protein having lipase activity;
(E 1 ) an isolated polynucleotide which encodes a protein consisting of the amino acid sequence shown in SEQ ID NO: 11;
(F 1 ) an isolated polynucleotide which encodes a protein consisting of an amino acid sequence comprising substitution, deletion, insertion and/or addition of 1 to 9 amino acids in the amino acid sequence shown in SEQ ID NO: 11 and having lipase activity; or
(G 1 ) an isolated polynucleotide which encodes a protein consisting of an amino acid sequence sharing an identity of at least 80% or more with the amino acid sequence shown in SEQ ID NO: 11 and having lipase activity,
wherein the stringent condition consists of hybridization at 65° C. in a solution containing 6 M urea, 0.4% sodium dodecyl sulfate (SDS), and 0.1×saline sodium citrate (SSC).
2. The isolated polynucleotide according to claim 1 , which is selected from (A 1 ′), (B 1 ′), (C 1 ′), (D 1 ′), (E 1 ′), (F 1 ′) or (G 1 ′) shown below:
(A 1 ′) an isolated polynucleotide which consists of all of the nucleotide sequence shown in SEQ ID NO: 10 or a part thereof covering nucleotides 25-801;
(B 1 ′) an isolated polynucleotide which is hybridizable under stringent conditions with a polynucleotide consisting of a nucleotide sequence complementary to the nucleotide sequence of the polynucleotide shown in (A 1 ′) and which encodes a protein having lipase activity;
(C 1 ′) an isolated polynucleotide which consists of a nucleotide sequence comprising substitution, deletion, insertion and/or addition of 1 to 9 nucleotides in the nucleotide sequence of the polynucleotide shown in (A 1 ′) and which encodes a protein having lipase activity;
(D 1 ′) an isolated polynucleotide which shares an identity of at least 80% or more with the nucleotide sequence of the polynucleotide shown in (A 1 ′) and which encodes a protein having lipase activity;
(E 1 ′) an isolated polynucleotide which encodes a protein consisting of the amino acid sequence shown in SEQ ID NO: 11;
(F 1 ′) an isolated polynucleotide which encodes a protein consisting of an amino acid sequence comprising substitution, deletion, insertion and/or addition of 1 to 9 amino acids in the amino acid sequence shown in SEQ ID NO: 11 and having lipase activity; or
(G 1 ′) an isolated polynucleotide which encodes a protein consisting of an amino acid sequence sharing an identity of at least 80% or more with the amino acid sequence shown in SEQ ID NO: 11 and having lipase activity
wherein the stringent condition consists of hybridization at 65° C. in a solution containing 6 M urea, 0.4% sodium dodecyl sulfate (SDS), and 0.1×saline sodium citrate (SSC).
3. The isolated polynucleotide according to claim 1 , which comprises (A 2 ), (B 2 ), (C 2 ), (D 2 ), (E 2 ), (F 2 ) or (G 2 ) shown below:
(A 2 ) an isolated polynucleotide which consists of all of the nucleotide sequence shown in SEQ ID NO: 15 or a part thereof covering at least nucleotides 247-1167 or 388-1164;
(B 2 ) an isolated polynucleotide which is hybridizable under stringent conditions with a polynucleotide consisting of a nucleotide sequence complementary to the nucleotide sequence of the polynucleotide shown in (A 2 ) and which encodes a protein having lipase activity;
(C 2 ) an isolated polynucleotide which consists of a nucleotide sequence comprising substitution, deletion, insertion and/or addition of 1 to 9 nucleotides in the nucleotide sequence of the polynucleotide shown in (A 2 ) and which encodes a protein having lipase activity;
(D 2 ) an isolated polynucleotide which shares an identity of at least 80% or more with the nucleotide sequence of the polynucleotide shown in (A 2 ) and which encodes a protein having lipase activity;
(E 2 ) an isolated polynucleotide which encodes a protein consisting of all of the amino acid sequence shown in SEQ ID NO: 16 or a part thereof covering at least amino acids 48-306;
(F 2 ) an isolated polynucleotide which encodes a protein consisting of an amino acid sequence comprising substitution, deletion, insertion and/or addition of 1 to 9 amino acids in the amino acid sequence of the protein shown in (E 2 ) and having lipase activity; or
(G 2 ) an isolated polynucleotide which encodes a protein consisting of an amino acid sequence sharing an identity of at least 80% or more with the amino acid sequence of the protein shown in (E 2 ) and having lipase activity
wherein the stringent condition consists of hybridization at 65° C. in a solution containing 6 M urea, 0.4% sodium dodecyl sulfate (SDS), and 0.1×saline sodium citrate (SSC).
4. The isolated polynucleotide according to claim 3 , which is selected from (A 2 ′), (B 2 ′), (C 2 ′), (D 2 ′), (E 2 ′), (F 2 ′) or (G 2 ′) shown below:
(A 2 ′) an isolated polynucleotide which consists of all of the nucleotide sequence shown in SEQ ID NO: 15 or a part thereof covering nucleotides 247-1167 or 388-1164;
(B 2 ′) an isolated polynucleotide which is hybridizable under stringent conditions with a polynucleotide consisting of a nucleotide sequence complementary to the nucleotide sequence of the polynucleotide shown in (A 2 ′) and which encodes a protein having lipase activity;
(C 2 ′) an isolated polynucleotide which consists of a nucleotide sequence comprising substitution, deletion, insertion and/or addition of 1 to 9 nucleotides in the nucleotide sequence of the polynucleotide shown in (A 2 ′) and which encodes a protein having lipase activity;
(D 2 ′) an isolated polynucleotide which shares an identity of at least 80% or more with the nucleotide sequence of the polynucleotide shown in (A 2 ′) and which encodes a protein having lipase activity;
(E 2 ′) an isolated polynucleotide which encodes a protein consisting of all of the amino acid sequence shown in SEQ ID NO: 16 or a part thereof covering at least amino acids 48-306;
(F 2 ′) an isolated polynucleotide which encodes a protein consisting of an amino acid sequence comprising substitution, deletion, insertion and/or addition of 1 to 9 amino acids in the amino acid sequence of the protein shown in (E 2 ′) and having lipase activity; or
(G 2 ′) an isolated polynucleotide which encodes a protein consisting of an amino acid sequence sharing an identity of at least 80% or more with the amino acid sequence of the protein shown in (E 2 ′) and having lipase activity,
wherein the stringent condition consists of hybridization at 65° C. in a solution containing 6 M urea, 0.4% sodium dodecyl sulfate (SDS), and 0.1×saline sodium citrate (SSC).
5. The isolated polynucleotide according to claim 1 , which is derived from the genus Tetrasphaera.
6. A vector carrying the isolated polynucleotide according to claim 1 .
7. A transformant transformed with the vector according to claim 6 .
8. The isolated polynucleotide according to claim 1 , wherein (D 1 ″) and (G 1 ″) are respectively:
(D 1 ″) an isolated polynucleotide which shares an identity of at least 90% or more with the nucleotide sequence of the polynucleotide shown in (A 1 ) and which encodes a protein having lipase activity; and
(G 1 ″) an isolated polynucleotide which encode a protein consisting of an amino acid sequence sharing an identity of at least 90% or more with the amino acid sequence shown in SEQ ID NO: 11 and having lipase activity.
9. The isolated polynucleotide according to claim 1 , wherein (D 1 ″) and (G 1 ″) are respectively:
(D 1 ″) an isolated polynucleotide which shares an identity of at least 95% or more with the nucleotide sequence of the polynucleotide shown in (A 1 ) and which encodes a protein having lipase activity; and
(G″) an isolated polynucleotide which encode a protein consisting of an amino acid sequence sharing an identity of at least 95% or more with the amino acid sequence shown in SEQ ID NO: 11 and having lipase activity.