Ex Parte Adams et alDownload PDFPatent Trial and Appeal BoardFeb 1, 201913328222 (P.T.A.B. Feb. 1, 2019) Copy Citation UNITED STA TES p A TENT AND TRADEMARK OFFICE APPLICATION NO. FILING DATE FIRST NAMED INVENTOR 13/328,222 12/16/2011 Whitney R. Adams JR. 73905 7590 02/05/2019 DENTONS US LLP P.O. BOX 061080 CHICAGO, IL 60606-1080 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 ATTORNEY DOCKET NO. CONFIRMATION NO. MONS:379US 1093 EXAMINER HWU,JUNE ART UNIT PAPER NUMBER 1661 NOTIFICATION DATE DELIVERY MODE 02/05/2019 ELECTRONIC 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. Notice of the Office communication was sent electronically on above-indicated "Notification Date" to the following e-mail address(es): patents.us@dentons.com PTOL-90A (Rev. 04/07) UNITED STATES PATENT AND TRADEMARK OFFICE BEFORE THE PATENT TRIAL AND APPEAL BOARD Ex parte WHITNEY R. ADAMS, BRIAN J. MARTINELL, JYOTI R. ROUT, and EDWARD J. WILLIAMS Appeal 2017-011383 Application 13/328,222 1 Technology Center 1600 Before ULRIKE W. JENKS, RACHEL H. TOWNSEND, and DAVID COTTA, Administrative Patent Judges. TOWNSEND, Administrative Patent Judge. DECISION ON APPEAL This is an appeal under 35 U.S.C. § 134 involving claims to a method for improving competency of plant embryo cells for bacterial-mediated transformation, which have been rejected as obvious. We have jurisdiction under 35 U.S.C. § 6(b ). We reverse. STATEMENT OF THE CASE "Plant tissues such as embryos can be obtained in large quantities by mechanical means .... " (Spec. 2.) "When stored for later use, [embryo] 1 Appellants identify the real party in interest as Monsanto Co., the parent company of Monsanto Tech. LLC. (Appeal Br. 1.) Appeal 2017-011383 Application 13/328,222 competency for transformation may be reduced." (Id.) "The present invention provides methods for improving competency of plant cells for bacterial-mediated transformation . . . . " (Id.) Claims 24, 25, 27, and 29--33 are on appeal. Claim 24 is representative and reads as follows: 24. A method for improving competency of plant embryo cells for bacterial-mediated transformation comprising: (a) contacting a mature plant embryo explant with an effective amount of a polyethylene glycol (PEG) containing composition having from about 10% to about 50% by volume of polyethylene glycol; and (b) transforming at least one cell of the mature plant embryo ex plant with a heterologous DNA sequence via bacterial-mediated transformation, wherein the transforming step (b) is performed after the contacting the step (a); wherein the PEG containing composition is removed prior to the transforming step (b ); wherein the mature plant embryo explant is excised from a dry seed; and wherein the improved competency is measured as an increase in transformation frequency. (Appeal Br. 9.) The following ground of rejection by the Examiner is before us on review: Claims 24, 25, 27, and 29-33 2 under 35 U.S.C. § 103 as unpatentable over Calabotta3 and Hongbo. 4 2 The Examiner mistakenly includes claim 26 in the Final Rejection. However, as Appellants note, claim 26 was cancelled prior to the issuance of that rejection. (Appeal Br. 1.) 3 Calabotta et al., US 8,362,317 B2, issued Jan. 29, 2013. 4 Hongbo et al., Impacts of PEG-6000 pretreatment for barley (Hordeum vulgare L.) seeds on the effect of their mature embryo in vitro culture and 2 Appeal 2017-011383 Application 13/328,222 DISCUSSION The Examiner finds that Calabotta teaches pre-culturing plant embryo explant prior to bacterial-mediated transformation. (Final Action 3.) The Examiner finds that the pre-culturing includes hydration ( also known as imbibition), for example, in soy inoculum (INO) or bean germination medium (BGM), and then the hydration liquid is removed and the explants are rinsed with sterile distilled water. (Id.) The Examiner notes that Calabotta further teaches that the explant may be dried or not prior to bacterial-mediated transformation, which transformation takes place when the explant is placed in PLANTCON. (Id. at 3--4.) The Examiner finds that Calabotta teaches that the plant seed from which the explant is obtained may be soybean, com, or cotton seed, and that the explant may be of "'various ages' which would include mature plant embryo explant." (Id. at 3.) The Examiner finds that Calabotta teaches that pre-culturing the explant "improve[ s] [the] transformation competency, transformation uniformity ([Calabotta] col. 31, lines 65---66), and possibly transformation frequency ([id. at] col. 32, lines 1-3)." (Id. at 4.) The Examiner recognizes that the pretreatment does not involve contacting the explant with PEG. The Examiner finds that Hongbo teaches pretreating mature barley embryos with PEG 6000 and then soaking the embryo in deionized water for 21 hours. (Id.) The Examiner notes that Hongbo teaches this process resulted in high percentage of callus induction and regenerated plantlets. primary investigation on its physiological mechanism, 41 Colloids and Surfaces B: Biointerfaces, 73-77 (2005). 3 Appeal 2017-011383 Application 13/328,222 (Id.) The Examiner also finds that Hongbo teaches the PEG pretreatment can improve tissue culture results by regulating mineral element and hormone content and can improve embryo quality by regulating imbibing course. (Id. at 5.) The Examiner concludes that it would have been obvious "to modify the method of Calabotta et al to substitute the hydration medium with PEG as taught by Hongbo et al because Hongbo et al taught that PEG 6000 pretreatment enhanced mature embryos (p. 75)." (Id.) According to the Examiner, the substitution would have been obvious particularly in light of the fact that Calabotta teaches that numerous hydration methods may be used prior to transformation. (Id.) We disagree with the Examiner's conclusion that Hongbo 's teaching i.e., pretreating seeds with PEG followed by imbibition of those seeds, would have rendered it obvious to substitute PEG for the INO or BGM imbibition medium in which the explant of Calabotta is pretreated prior to transformation of the explant. 5 As Appellants note (Appeal Br. 2-3; Reply Br. 4 ), Hongbo describes effects of PEG on certain growth parameters of seeds after treatment with PEG and imbibition medium. (Hongbo 74 § "2. Materials and Methods" and§ "3. Results".) In particular Hongbo notes that "10% PEG-6000 pretreatment could effectively retard the leakage of solutes and macromolecules from the seeds." (Id.§ 3.1.) Hongbo explains that [ t ]hese phenomena suggested that proper PEG-6000 pretreatment could slow down the soluble leakage, which was 5 We note that the Examiner does not assert that adding PEG prior to imbibition with a growth medium of the dried explant of Calabotta would have been obvious. 4 Appeal 2017-011383 Application 13/328,222 beneficial to subsequent morphogenesis including seed germination and in vitro culture response of the mature seeds. (Id.) Hongbo determined that PEG-6000 pretreatment with imbibition of seed resulted in better effect of root emergence, bud emergence, better callus induction, and regenerated plantlet, whether the pretreated seed was cultured or mature embryo from pretreated seed was cultured. (Id. at 75 § 3.4.) However, the Examiner does not identify, and we do not find, anything in Hongbo to suggest using PEG as an imbibition medium by itself, much less what benefits could be expected to an explant so treated. Moreover, the Examiner has not explained why the teaching in Hongbo that PEG-6000 pretreatment followed by treating seeds with imbibition medium results in better root and bud emergence, callus induction, and regenerated plantlet when an embryo explant from that seed is cultured would have caused the ordinary artisan to expect that pretreatment of an embryo explant itself with PEG as the imbibition liquid in Calabotta would have an expectation of any benefit to that embryo explant or for subsequent transformation of that explant. Nor has the Examiner explained why the teaching in Hongbo that PEG-6000 pretreatment followed by treating seeds with imbibition medium lowers solute leakage from the seed would have caused the ordinary artisan to expect that pretreatment of an embryo explant itself with only PEG as the imbibition liquid in Calabotta would have an expectation of any benefit to that embryo explant or for subsequent transformation of that explant. As the Examiner notes, Calabotta describes a method in which explant from soy seed is hydrated in a carbohydrate based media prior to transformation. (Final Action 3; Calabotta 15-16 (Example 4 ). ) Example 12 of Calabotta demonstrates a process involving pre-culturing the explants 5 Appeal 2017-011383 Application 13/328,222 in carbohydrate based medium, including INO, BGM (both of which also contain a number of mineral salts), or soy organogenic (which includes a number of mineral salts and B vitamins). (Calabotta 30: 1-36 (Example 12).) The process stimulates "the metabolic activity" of the dry excised explants prior to bacterial transformation to "increas[ e] their transformation competency." (Id.) Thus, we find that Calabotta teaches that a carbohydrate based medium with salts is important for the pre-treatment of the explant in order to achieve the increased transformation competency of the explant. Hongbo' s teaching that PEG-6000 pretreatment of a seed could effectively retard the leakage of solutes and macromolecules from the seed when undergoing imbibition (Hongbo 7 4 (3 .1: "Fig. 1 showed that 10% PEG-6000 pretreatment could effectively retard the leakage of solutes and macromolecules from the seeds by comparing the control ones"; 3.2: "There was different transfer of mineral elements with various amounts between embryos and endosperms of the seeds.")), or that seed explant from seed that was pretreated with PEG and carbohydrate based imbibition liquid had improved root and bud emergence and better callus induction and regenerated plantlet as compared to explant from seed that was not so pretreated with PEG before imbibition (Hongbo 74 (3.4: "From Table 2, the result showed that: [] PEG-6000 pretreatment could obviously raise in vitro culture effect whether seeds or mature embryos were used as explants"; Hongbo 7 6 ("this investigation combines PEG-6000 pretreatment, corresponding index in physiology with in vitro culture effect and embryos and endosperms in the pretreated seeds were detected individually (emphasis added)), does not support the Examiner's simple substitution conclusion (Ans. 6) of PEG for the carbohydrate medium in the Calabotta 6 Appeal 2017-011383 Application 13/328,222 explant demonstration discussed above. We do not find any evidence of record relied on by the Examiner in Hongbo or Calabotta that would suggest a reasonable expectation of success of stimulating metabolic activity of embryo explant so as to increase transformation competency by pretreatment with PEG of the explant without the presence of a carbohydrate and mineral salt medium. We disagree with the Examiner (Ans. 7) that Hongbo provides a suggestion that "pretreatment with PEG has some importance in biotechnology breeding or transformation." (Emphasis added.) Hongbo at page 7 6, which the Examiner relies on, while mentioning that PEG is used in protoplast fusion, does not suggest that PEG would have a benefit by itself in stimulating metabolic activity of embryo explant or that it would somehow otherwise improve competency of embryo explant by itself. Hongbo merely summarizes that its research shows that PEG pretreatment of seeds promotes in vitro culture of an explant when provided in conjunction with imbibition medium because it controls leakage of minerals from the seed and thus provides a benefit to an explant when such a seed is subsequently cultured. We conclude that the Examiner is mixing apples and oranges in the conclusion that Hongbo 's improved embryo quality from pretreatment of seed with PEG prior to imbibition of the seed is relatable to Calabotta's improved metabolic activity in embryo explant due to pre- culturing dry embryo explant with a carbohydrate and mineral salt based medium. For the reasons discussed above, we determine that the Examiner has not set forth a factual basis sufficient to support the specified rejection for obviousness. Accordingly, we reverse the Examiner's rejection of claims 7 Appeal 2017-011383 Application 13/328,222 24, 25, 27, and 29-33 under 35 U.S.C. § 103 as unpatentable over Calabotta and Hongbo. SUMMARY We reverse the rejection of claims 24, 25, 27, and 29-33 under 35 U.S.C. § 103 as unpatentable over Calabotta and Hongbo. REVERSED 8 Copy with citationCopy as parenthetical citation