Ex Parte Koizumi et alDownload PDFPatent Trial and Appeal BoardDec 11, 201210940026 (P.T.A.B. Dec. 11, 2012) Copy Citation UNITED STATES PATENT AND TRADEMARK OFFICE UNITED STATES DEPARTMENT OF COMMERCE United States Patent and Trademark Office Address: COMMISSIONER FOR PATENTS P.O. Box 1450 Alexandria, Virginia 22313-1450 www.uspto.gov APPLICATION NO. FILING DATE FIRST NAMED INVENTOR ATTORNEY DOCKET NO. CONFIRMATION NO. 10/940,026 09/14/2004 Satoshi Koizumi 00766.000020.2 4992 5514 7590 12/11/2012 FITZPATRICK CELLA HARPER & SCINTO 1290 Avenue of the Americas NEW YORK, NY 10104-3800 EXAMINER RAGHU, GANAPATHIRAM ART UNIT PAPER NUMBER 1652 MAIL DATE DELIVERY MODE 12/11/2012 PAPER Please find below and/or attached an Office communication concerning this application or proceeding. The time period for reply, if any, is set in the attached communication. PTOL-90A (Rev. 04/07) UNITED STATES PATENT AND TRADEMARK OFFICE __________ BEFORE THE PATENT TRIAL AND APPEAL BOARD __________ Ex parte SATOSHI KOIZUMI, KATSUTOSHI SASAKI, TETSUO ENDO, KAZUHIKO TABATA, and AKIO OZAKI __________ Appeal 2011-000965 Application 10/940,026 Technology Center 1600 __________ Before ERIC GRIMES, JEFFREY N. FREDMAN, and SHERIDAN K. SNEDDEN, Administrative Patent Judges. SNEDDEN, Administrative Patent Judge. DECISION ON APPEAL This is an appeal under 35 U.S.C. § 134 involving claims to a process for producing a complex carbohydrate. The Examiner has rejected the claims as obvious. We have jurisdiction under 35 U.S.C. § 6(b). We reverse. Appeal 2011-000965 Application 10/940,026 2 STATEMENT OF THE CASE Claims 2, 3, 5, 7-14, 16-18, 20 and 72-77 are on appeal. Claims 2 and 3 are independent and representative. The method of the invention is claimed as a one-step process in claim 2 and a two-step process in claim 3. (See e.g., Reply Br. 2-3.) Claims 2 and 3 provide as follows (emphasis added): 2. A process for producing a complex carbohydrate, which comprises: selecting, as enzyme sources, (a) a culture of a microorganism belonging to the genus Corynebacterium and capable of producing NTP from a nucleotide precursor, or a treated product of the culture, (b) a culture of at least one microorganism belonging to the genus Escherichia or Corynebacterium, said culture being capable of producing a sugar nucleotide from a sugar and NTP, or a treated product of the culture and (c) a culture at least one microorganism belonging to the genus Escherichia or Corynebacterium, said culture being capable of intracellularly producing a complex carbohydrate from a sugar nucleotide and a complex carbohydrate precursor, or a treated product of the culture; allowing the enzyme sources, the nucleotide precursor, the sugar and the complex carbohydrate precursor to be present in an aqueous medium to form and accumulate the complex carbohydrate in the aqueous medium; and recovering the complex carbohydrate from the aqueous medium, wherein the sugar nucleotide is a uridine diphosphate compound, a guanosine diphosphate compound or a cytidine monophosphate compound, and wherein the treated product of culture is a concentrated product of the culture, a dried product of the culture, cells obtained by centrifuging the culture, a dried product of the cells, a freeze-dried product of the cells, a surfactant-treated product of the cells, a solvent-treated product of the cells, an Appeal 2011-000965 Application 10/940,026 3 enzyme-treated product of the cells, or an immobilized product of the cells. 3. A process for producing a complex carbohydrate, which comprises: (I) selecting, as enzyme sources, (a) a culture of a microorganism belonging to the genus Corynebacterium and capable of producing NTP from a nucleotide precursor, or a treated product of the culture, and (b) a culture of at least one microorganism belonging to the genus Escherichia or Corynebacterium capable of producing a sugar nucleotide from a sugar and NTP, or a treated product of the culture; allowing the enzyme sources, the nucleotide precursor and the sugar to be present in an aqueous medium to form and accumulate the sugar nucleotide in the aqueous medium; and recovering the sugar nucleotide from the aqueous medium, and (II) selecting, as an enzyme source, a culture of a microorganism belonging to the genus Escherichia or Corynebacterium capable of intracellularly producing a complex carbohydrate from a sugar nucleotide and a complex carbohydrate precursor, or a treated product of the culture; allowing the enzyme source, the complex carbohydrate precursor and the sugar nucleotide prepared by (1) to be present in an aqueous medium to form and accumulate the complex carbohydrate in the aqueous medium; and recovering the complex carbohydrate from the aqueous medium, wherein the sugar nucleotide is a uridine diphosphate compound, a guanosine diphosphate compound or a cytidine monophosphate compound, and wherein the treated product of culture is a concentrated product of the culture, a dried product of the culture, cells obtained by centrifuging the culture, a dried product of the cells, a freeze-dried product of the cells, a surfactant-treated product of the cells, a solvent-treated product of the cells, an Appeal 2011-000965 Application 10/940,026 4 enzyme-treated product of the cells, or an immobilized product of the cells. The claims stand rejected as follows: I. Claims 2, 3, 5, 7-9, 16-18, 20 and 75-77 under 35 U.S.C. § 103(a) as being unpatentable over the combination of Roth (WO 95/02683, published Jan. 26, 1995), Snetkova et al. (Translated from KHIMIYA PRIRODNYKH SOEDINENII, 1988, No.2, pages 221- 226) and Nyholm at al. (A method for production of 13 C/N 15 double labelled RNA in E. Coli, and subsequent in vitro synthesis of ribonucleotide 5’ triphosphates, 30 J. BIOCHEM. BIOPHYS. METHODS 59- 68 (1995)). II. Claims 10-14 and 72-73 under 35 U.S.C. § 103(a) as being unpatentable over the combination of Roth, Snetkova, Nyholm and DeFrees (WO 96/32491, published Oct. 17, 1996). III. Claim 74 under 35 U.S.C. § 103(a) as being unpatentable over the combination of Roth, Snetkova, Nyholm, DeFrees and Aoki at al. (Cloning of a Streptococcus mutans Glucosyltransferase Gene Coding for Insoluble Glucan Synthesis, 53 INFN. IMMUN. 587-594 (1996)). Each rejection set forth by the Examiner relies on the disclosures of Roth, Snetkova and Nyholm. Because the same issue is dispositive for each rejection, we will consider them together. I. Issue The Examiner finds that the Appeal 2011-000965 Application 10/940,026 5 claims as written encompass[ ] any one of the steps in the alternative for selecting enzyme sources from (a)-(c) including free enzymes or crude enzyme extracts as the source of the enzyme(s) and contrary to the Appellants‟ arguments that indicate claims are: (i) limited to encompasses/requires „all the three steps‟ in a sequential manner in said method; and (ii) only intact live cells are required in the said process or intracellular production of complex carbohydrate. (Ans. 17.) As such, the Examiner finds that “[t]he cited references are in congruence with the obviousness rejection and teach all limitations of the instant claims.” (Id. at 18.) Appellants contend that “[t]he use of the word „and‟ in this context, rather than „or,‟ makes clear that the claims are not written in the alternative.” (Reply Br. 7; emphasis in original.) Appellants further argue “that no reference teaches using cell culture to produce a sugar nucleotide” and “that no reference teaches using cell culture to produce a complex carbohydrate intracellularly.” (Reply Br. 14; emphasis in original.) The issue presented is: Does the evidence of record support the Examiner‟s findings that the combination of references cited teach or suggest all limitations of claim 2? Findings of Fact FF1. Roth discloses a method of synthesizing saccharide compositions where “an acceptor moiety is contacted with at least one donor saccharide in the presence of at least one cell surface-bound glycosyltransferase specific for catalyzing the coupling of the acceptor moiety with the donor saccharide.” (Roth, Abstract.) Appeal 2011-000965 Application 10/940,026 6 FF2. Roth discloses that “[t]he acceptor moiety used is a carbohydrate, a protein, a glycoprotein, a lipid, or a glycolipid.” (Id.) FF3. Roth discloses that “[t]he donor saccharide is provided in the form of a nucleoside mono- or diphosphate sugar.” (Roth 7, ll. 17-18.) FF4. Roth discloses as follows: In a preferred embodiment, a bioreactor containing a cell culture that expresses a given conjugate sugar nucleotide donor, due to transfection of cDNAs that encode the enzymes necessary for synthesis of this saccharide donor, is allowed to interact with another bioreactor containing a cell culture which has surface expression of the appropriate glycosyltransferase for the conjugate sugar nucleotide. (Roth 17, last ¶.) FF5. Snetkova discloses that a set of enzymes is present in E. coli and Corynebacterium species for “synthesizing nucleoside 5′-triphosphates (NTPs) from bases and 5-phosphoribosyl l-pyrophosphate (PRPP) without the isolation of the intermediate products” and allows for the “elimination of the stage of forming nucleosides.” (Snetkova, 221.) FF6. Nyholm discloses “an enhanced method for the large scale production of high quality 13 C/ 15 N labelled NTPs” in E. coli cells. (Nyholm, Abstract.) Principles of Law The meaning given to claim terms must be consistent with how they would be read by those of ordinary skill in the art. See Phillips v. AWH Corp., 415 F.3d 1303, 1312-13 (Fed. Cir. 2005)(“[T]he words of a claim „are generally given their ordinary and customary meaning.‟ … [T]he ordinary and customary meaning of a claim term is the meaning that the Appeal 2011-000965 Application 10/940,026 7 term would have to a person of ordinary skill in the art in question at the time of the invention.”). When determining whether a claim is obvious, an examiner must make “a searching comparison of the claimed invention — including all its limitations — with the teaching of the prior art.” In re Ochiai, 71 F.3d 1565, 1572 (Fed. Cir. 1995). As the Supreme Court pointed out in KSR Int'l Co. v. Teleflex Inc., 550 U.S. 398, 418 (2007), “a patent composed of several elements is not proved obvious merely by demonstrating that each of its elements was, independently, known in the prior art.” Rather, the Court stated: [I]t can be important to identify a reason that would have prompted a person of ordinary skill in the relevant field to combine the elements in the way the claimed new invention does … because inventions in most, if not all, instances rely upon building blocks long since uncovered, and claimed discoveries almost of necessity will be combinations of what, in some sense, is already known. Id. at 418-419 (emphasis added); see also id. at 418 (requiring a determination of “whether there was an apparent reason to combine the known elements in the fashion claimed by the patent at issue”) (emphasis added). Similarly, as our reviewing court has stated, “obviousness requires a suggestion of all limitations in a claim.” CFMT, Inc. v. Yieldup Intern. Corp., 349 F.3d 1333, 1342 (Fed. Cir. 2003). Analysis We agree with Appellants that independent claims 2 and 3 require selection of a culture or treated product of the culture from each of the enzyme sources (a), (b) and (c). We find that the Examiner has not provided Appeal 2011-000965 Application 10/940,026 8 an adequate basis for requiring “and” to be interpreted as “or” in the context of claims 2 and 3. Having determined the scope of Appellants‟ claims, we agree with Appellants that the cited references do not support a prima facie case of obviousness. Like Appellants, we are unable to find where in the references it is either taught or suggested that each of the three enzyme sources recited in claims 2 and 3 are used sequentially in a method for producing a complex carbohydrate. (See e.g., App. Br. 9-10.) For example, none of the references appear to disclose a process for producing sugar nucleotide from NTP. (See e.g., step (b) of claim 2; Reply Br. 14.) We further agree that the Examiner has not adequately explained how the references would have suggested using a cell culture to produce a complex carbohydrate intracellularly, as required by step (c) of claim 2 and step (II) of claim 3. (See e.g., Reply Br. 14.) Since all claim limitations are not taught or suggested by the applied prior art, the Examiner has failed to establish a prima facie case for the obviousness of independent claims 2 and 3. Conclusion of Law We conclude that the preponderance of the evidence of record does not support the Examiner‟s conclusion that the combination of Roth, Snetkova and Nyholm discloses a method having all limitations of independent claims 2 and 3 and dependent claims thereto (claims 5, 7-14, 16-18, 20 and 72-77). We thus reverse the rejections under 35 U.S.C. § 103(a) that rely on the teachings of Roth, Snetkova and Nyholm. Appeal 2011-000965 Application 10/940,026 9 SUMMARY We reverse the rejection of claims 2, 3, 5, 7-9, 16-18, 20 and 75-77 under 35 U.S.C. § 103(a) as being unpatentable over the combination of Roth, Snetkova, and Nyholm. We reverse the rejection of claims 10-14 and 72-73 under 35 U.S.C. § 103(a) as being unpatentable over the combination of Roth, Snetkova, Nyholm and DeFrees. We reverse the rejection of claim 74 under 35 U.S.C. § 103(a) as being unpatentable over the combination of Roth, Snetkova, Nyholm, DeFrees and Aoki. REVERSED cdc Copy with citationCopy as parenthetical citation