`Ex. 2001, Jaczynski Declaration
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`IN THE UNITED STATES PATENT AND TRADEMARK OFFICE
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`BEFORE THE PATENT TRIAL AND APPEAL BOARD
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`RIMFROST AS
`Petitioner
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`v.
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`AKER BIOMARINE ANTARCTIC AS
`Patent Owner
`
`
`CASE IPR: IPR2020-01534
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`U.S. Patent No. 10,010,567 B2
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`Declaration of Dr. Jacek Jaczynski
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`AKER EXHIBIT 2001 PAGE 0001
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`Inter Partes Review of US 10,010,567
`Ex. 2001, Jaczynski Declaration
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`I, Jacek Jaczynski, Ph.D., declare as follows:
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`1. My experience and qualifications are summarized in my curriculum vitae, a
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`copy of which is attached hereto as Appendix A.
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`2. I have been asked by counsel to review relevant materials and render my
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`expert opinion in connection with technical matters related to the petition for inter
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`partes review of U.S. Patent 10,010,567 ("the '567 patent"). I understand that the
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`parties involved in this IPR proceeding are the Petitioner, Rimfrost AS
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`("Rimfrost"), and the Patent Owner, Aker BioMarine Antarctic AS ("Aker").
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`3. I am being compensated for my time in connection with developing and
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`rendering my opinions in this matter at the rate of $500/hour. However, my
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`compensation is not dependent on the outcome of this proceeding. I am not an
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`employee, consultant, or contractor of either party.
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`4. I understand that Rimfrost is seeking cancellation of various claims of the
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`'567 patent based on the argument that such claims would have been obvious in
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`view of the teachings of the prior art. I understand that the specific grounds are as
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`follows:
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`2
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`AKER EXHIBIT 2001 PAGE 0002
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`Inter Partes Review of US 10,010,567
`Ex. 2001, Jaczynski Declaration
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`Ground 1: Claims 1-5, 7-11 and 15-17 are alleged to be obvious under 35
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`U.S.C. 103(a) over the combination of Sampalis I, Bottino II and Randolph;
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`Ground 2: Claims 6, 14 and 20 are alleged to be obvious under 35 U.S.C.
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`103(a) over the combination of Sampalis I, Bottino II, Randolph and Breivik
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`II;
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`Ground 3: Claims 12 and 18 are alleged to be obvious under 35 U.S.C.
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`103(a) over the combination of Sampalis I, Bottino II, Randolph and Bottino
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`I;
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`Ground 4: Claims 13 and 19 are alleged to be obvious under 35 U.S.C.
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`103(a) over the combination of Sampalis I, Bottino II, Randolph, Fricke,
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`Yamaguchi and Hardardottir;
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`5.
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`In order to render my opinions in this matter, I have reviewed the following
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`materials:
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`• The '567 patent (Ex. 1001);
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`AKER EXHIBIT 2001 PAGE 0003
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`• The declaration of Rimfrost's expert, Dr. Tallon (Ex. 1006) and the
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`following Exhibits referred to therein: Exs. 1007, 1008, 1010; 1011, 1012,
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`1032, 1033, 1035, 1036, 1037 and 1038;
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`• Ex. 2002 (Freeman and West);
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`• Ex. 2003 (Retardation factor definition);
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`• Ex. 2019 (Tallon Deposition Testimony);
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`• Any other materials referenced directly or indirectly in my
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`declaration.
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`6.
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`Throughout this Declaration, I refer to my understanding of certain legal
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`standards. I have been informed of these legal standards by Aker’s attorneys. I am
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`not an attorney, and I am relying only on instructions from Akers’ attorneys for
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`these legal standards. I have applied these understandings in my analysis as
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`detailed below.
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`I. RELEVANT FIELD AND DESCRIPTION OF PERSON HAVING
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`ORDINARY SKILL IN THE ART
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`7. The relevant field for the '567 patent includes extraction of lipids from
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`natural sources. I consider myself to be an expert in the relevant field.
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`AKER EXHIBIT 2001 PAGE 0004
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`8. I understand that Rimfrost has argued that as of the priority date of the '567
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`Ex. 2001, Jaczynski Declaration
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`Patent, a Person of Ordinary Skill in the Art (POSITA) would have held an
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`advanced degree in marine sciences, biochemistry, organic (especially lipid)
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`chemistry, chemical or process engineering, or associated sciences with
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`complementary understanding, either through education or experience, of organic
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`chemistry and in particular lipid chemistry, chemical or process engineering,
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`marine biology, nutrition, or associated sciences; and knowledge of or experience
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`in the field of extraction. In addition, a POSITA would have had at least five years'
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`applied experience. For the purposes of this proceeding, I will accept that
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`definition of a POSITA.
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`II. CLAIM CONSTRUCTION
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`9. I understand that the meanings of the claim terms are to be understood from
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`the perspective of a POSITA. I understand that claim construction begins with the
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`ordinary and customary meanings of the terms used in the claims. I further
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`understand that the meanings of terms used in the claims should be understood
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`primarily in view of the intrinsic record, including the specification and file
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`history. I further understand that IPR proceedings on petitions filed after
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`November 13, 2018 do not utilize the broadest reasonable broadest reasonable
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`interpretation standard.
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`5
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`AKER EXHIBIT 2001 PAGE 0005
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`10. I understand that the first step in analyzing Rimfrost's grounds for
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`Inter Partes Review of US 10,010,567
`Ex. 2001, Jaczynski Declaration
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`unpatentability is to determine the meaning of the terms in the involved claims of
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`the '567 patent.
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`11. Rimfrost offer the following construction of terms contained in the claims:
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`• “krill oil” means “lipids extracted from krill.”
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`• “astaxanthin ester” means “[a]n astaxanthin molecule in which one or both
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`of the hydroxyl groups are replaced by a fatty acid tail connected to the
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`astaxanthin molecule through an ester bond.”
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`• “phytonutrient” means “a plant-derived compound that has a positive impact
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`on human health or nutrition.”
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`12.
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`It is my opinion that the terms of the claims should be given their plain and
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`ordinary meaning. For the purposes of this declaration, I will accept Rimfrost’s
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`construction of the claim terms.
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`III. ANALYSIS OF RIMFROST'S PROPOSED GROUNDS FOR
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`INVALIDITY
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`13. I understand that a claim of an issued patent can be found to be invalid if the
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`claim would have been obvious in view of the prior art. I understand that this
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`AKER EXHIBIT 2001 PAGE 0006
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`determination is made from the perspective of a person having ordinary skill in the
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`art who is presumed to be aware of all prior art.
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`14. I further understand that the determination of obviousness involves
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`consideration of the scope and content of the prior art, the differences between the
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`prior art and the claims, and the level of ordinary skill in the art. I also understand
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`that secondary factors of non-obviousness can be considered, such as commercial
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`success, long-felt but unsolved needs, failure of others, industry praise, etc.
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`15.
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`I understand that a POSITA provides a reference point from which the prior
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`art and claimed invention should be viewed. This reference point prevents one
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`from using his or her own insight or hindsight in deciding whether a claim is
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`obvious. Thus, “hindsight reconstruction” cannot be used to combine references
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`together to reach a conclusion of obviousness.
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`16. I have been asked to give my opinions as to whether Claims 1-20 of the '567
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`Patent would have been obvious to a person having ordinary skill in the art in
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`accordance with the grounds set forth by Rimfrost in its petition.
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`17. Claims 1 and 15 of the '567 Patent are independent claims. Claims 2-14 of
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`the '567 Patent are all dependent on Claim 1, and claims 16-20 of the '567 Patent
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`are all dependent on Claim 15.
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`7
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`AKER EXHIBIT 2001 PAGE 0007
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`Independent Claim 1 reads as follows:
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`1.
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`Encapsulated krill oil comprising a capsule containing Euphausia
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`superba krill oil suitable for oral administration, said krill oil comprising
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`greater than 30% phosphatidylcholine w/w of said krill oil, less than 3% free
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`fatty acids w/w of said krill oil and astaxanthin esters.
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`Independent Claim 15 reads as follows:
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`15. Encapsulated krill oil comprising a soft gel capsule containing Euphausia
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`superba krill oil suitable for oral administration, said krill oil comprising
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`greater than 30% phosphatidylcholine w/w of said krill oil, less than 3% free
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`fatty acids w/w of said krill oil, less than about 3% lysophosphatidylcholine
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`w/w of said krill oil and at least 100 mg/kg astaxanthin esters.
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`18. Both independent claims are included in Ground 1. As explained in detail
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`below, it is my opinion that that the references cited in Ground 1 do not teach or
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`suggest the claim element of “less than 3% free fatty acids.” Specifically, Rimfrost
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`contends that Bottino II provides the “less than 3% free fatty acid” limitation.
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`Rimfrost and its expert have misinterpreted the data in Bottino II.
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`19. Ground 1 advanced by Rimfrost applies to independent claim 1 and
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`dependent claims 2-10, which depend on claim 1. The remaining Grounds (2, 3
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`AKER EXHIBIT 2001 PAGE 0008
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`and 4) apply to claims that are dependent on the claims addressed in Ground 1. I
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`understand that where the references combined against Ground 1 do not render that
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`claim obvious, the dependent claims are not obvious either.
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`A. Ground 1 fails because the combined references do not teach each
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`element of the claims
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`24. I understand that Rimfrost asserts that Claims 1-5, 7-11 and 15-17 are
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`alleged to be obvious under 35 U.S.C. 103(a) over the combination of Sampalis I,
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`Bottino II and Randolph. I understand that Rimfrost made the following argument
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`in its Petition:
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`As detailed previously, Table 2 of Bottino II discloses a Euphausia superba
`extract with 48% phosphatidylcholine and at most 2% free fatty acids.
`Exhibit 1038, p. 0003; supra, pp. 21-22.5 Tallon Decl. (Exhibit 1006), ¶ 174.
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`Petition at 46. Rimfrost further argued:
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`Table 2 also discloses that “unknowns” constituted 2 ± 22 (i.e., 2 ± 22%) of
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`that krill extract. Since free fatty acids would be included in this “unknown”
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`fraction, the free fatty acid content of this extract would be at most 2%.
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`Tallon Decl. (Exhibit 1006), ¶ 174. Notably, the free fatty acid content
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`disclosed in Bottino II is consistent with Fricke’s disclosure of a krill extract
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`with 1-3% free fatty acids. Exhibit 1010, pp. 0002-0003. See Tallon Decl.
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`(Exhibit 1006), ¶¶ 171-176.
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`AKER EXHIBIT 2001 PAGE 0009
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`Petition at 22. The reliance on Bottino II for the claim element of “less than 3%
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`free fatty acids” is demonstrated by reference to Petitioner’s claim charts, excerpts
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`of which are provided here for claim 1:
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`And claim 15:
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`25. At ¶174 of his Declaration, Dr. Tallon makes the following observations
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`with respect to Table 2 of Bottino II:
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`174. Bottino II Table 2 provides a breakdown of the lipids of two types of
`krill: E. superba and E. crystallorophias, and discloses extracted Euphausia
`superba polar krill oil containing 58% total phospholipids, 48%
`phosphatidylcholine (PC), 36% triglycerides, 1% lysophosphatidylcholine
`(Lyso PC) by weight of krill oil, and 2% Unknown.
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`Dr. Tallon goes on to argue:
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`AKER EXHIBIT 2001 PAGE 0010
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`The ‘Unknown’ lipid fraction in Bottino II Table 2 is noted in the footnote
`as presenting between the triglyceride and diglyceride fractions, and that the
`amount recovered was too small to characterize further. A POSITA would
`understand that, while not identified, this fraction would include any free
`fatty acids that are present in the krill lipids. Thus Bottino II discloses a free
`fatty acid content for Station 11 of at most 2%.
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`26. The data reported in Table II of Bottino II was obtained by a Thin Layer
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`Chromatography (TLC) method described in Freeman and West 1966 (Ex. 2002).
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`In TLC, compounds in a sample are separated on a thin layer of adsorbent material,
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`typically a coating of silica gel on a glass plate or plastic sheet. As disclosed in
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`Bottino II:
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`For quantitative fractionation of lipid classes 20-40 mg of lipids were
`separated by the method of Freeman & West (1966) modified as follows: (a)
`Silica gel without binder (Adsorbosil-5, Applied Science) was used instead
`of silica gel-G. (b) Acetic acid was eliminated from the solvent mixture No.
`1 to simplify the drying between developments. (c) Quantitation of the spots
`was done by gravimetry and not by colorimetry of dichromate reduction.
`The gravimetric estimation required the use of the following procedure:
`Once separated by TLC and located with dichlorofluorescein spray, the spots
`were scraped off the plates, extracted six times with 4 ml (each) of a mixture
`of chloroform-methanol-acetic acid-water (50 : 39 : 1 : 10, v/v) (Arvidson,
`1968). The extracts were filtered through fine pore sintered glass funnels
`into test-tubes, then 8 ml of 4 M ammonium hydroxide were added and the
`mixture shaken and centrifuged. The resulting upper phase, which contained
`the DCF, was discarded and to the lower phase was added 8 ml of 50% (v/v)
`methanol in water. After the addition of anhydrous sodium sulfate, the liquid
`was filtered through a fine pore sintered glass funnel containing a layer of
`anhydrous sodium sulfate. The filtrate was then evaporated under vacuum
`and the residue was weighed. Using known amounts of total lipids in each
`determination, it was possible to estimate the recovery. Any result showing
`less than 80 per cent recovery was discarded and the fractionation repeated.
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`AKER EXHIBIT 2001 PAGE 0011
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`Ex. 2001, Jaczynski Declaration
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`Ex. 1038 at 0002. Thus, Bottino II performed a modified version of the TLC
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`method of Freeman and West (Ex. 2002) and quantified the amounts of lipid
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`classes separated on TLC plates by gravimetry, which is a weighing method.
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`27. As noted by Dr. Tallon, the footnote for the “unknown fraction” reads as
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`follows:
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`§Rf between those of triglycerides and diglycerides. The recovered amount
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`of this fraction was too small for further characterization.
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`Ex. 1038 at 0003. Rf refers to the retardation factor, which in thin layer
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`chromatography (TLC) is defined as the ratio of the distance traveled by the center
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`of a spot to the distance traveled by the solvent front. For example, Rf is defined in
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`the IUPAC Goldbook. Ex. 2003 is a screenshot of the definition from the online
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`version of the IUPAC Goldbook as of July 20, 2021. In lay terms, the Rf value
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`when used in relation to TLC is a measure of how far an analyte travels on a TLC
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`plate. The direction of travel in TLC plates is generally from the bottom of the
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`plate to the top. Different analytes such as triglycerides, diglycerides,
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`phospholipids and free fatty acids will have different Rf values, indicating that they
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`travel different distances on the TLC plate. A high Rf value indicates that the
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`compound has travelled far up the plate and is less polar, while a lower Rf value
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`indicates that the compound has not travelled far, and is more polar.
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`AKER EXHIBIT 2001 PAGE 0012
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`28. The data in Bottino II do not support Dr. Tallon’s conclusion that the
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`unknown fraction contained the free fatty acids and that the free fatty acid content
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`of the Bottino II extract would thus be less than 2%. Specifically, Figure 1 of
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`Freeman and West demonstrates that free fatty acids have an Rf value that is lower
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`than that of diglycerides and triglycerides in the solvent systems utilized and
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`therefore the free fatty acids do not travel as far as triglycerides or diglycerides in
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`solvent system 1 (panel a of Fig. 1 or the combination of solvent systems 1 and 2
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`(panel c in Fig. 1). Fig.1 is reproduced for reference:
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`AKER EXHIBIT 2001 PAGE 0013
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`Ex. 2002 at 0002. As can be seen, in each solvent system utilized, free fatty acids
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`(designated FA in Figure 1) migrate a shorter distance than triglycerides (TG in
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`Figure 1) and diglycerides (DG in Figure 1), and farther than phospholipids (PL in
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`Figure 1). The alterations of the Freeman and West solvent systems noted in
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`Bottino II would not be expected to change this migration pattern. Thus, Bottino
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`II’s “unknowns,” which migrated between the triglycerides and diglycerides, could
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`not include free fatty acids as concluded by Dr. Tallon.
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`AKER EXHIBIT 2001 PAGE 0014
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`29. As a result, Bottino II contains no information on the free fatty acid content
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`of its extracts. Given the content of diglycerides, lysophosphatidylcholine, and
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`phosphatidylglycerol reported in Table 2, it would be reasonable to assume that
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`free fatty acids were present in the sample but not reported. Bottino II does not
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`provide photographs of the TLC plates. One could speculate that the lack of data
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`on free fatty acid content is due to poor resolution of spots representing lipids on
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`the TLC plates, but without pictures of the TLC plates this cannot be determined.
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`It is notable that when the Station 8 and Station 11 data for E. superba are
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`compared, the values for PC and PE are missing from the Station 8 data. This
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`indicates that the data is not reliable and would be disregarded by a POSITA even
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`for anecdotal use. Bottino II was published in 1975. By 2006, it was unlikely that
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`a paper with these types of problems with the data would be accepted for
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`publication.
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`30. Furthermore, some of the values reported in Table 2 have extremely high
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`levels of standard deviation (SD). For example, the “unknowns” are reported as
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`2% ± 22% and diglycerides as reported as 4% ± 5% for the Station 11 sample, and
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`as 21 % and 17% in the Station 8 sample, respectively. Due to this high degree of
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`variability, a POSITA would be discouraged from drawing any conclusions about
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`the actual lipid contents of the extracts, much less the free fatty acid content. In
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`AKER EXHIBIT 2001 PAGE 0015
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`fact, from my experience, which would be consistent with that of a POSITA,
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`whenever I see such a high SD as 2 ± 22 (the SD is about 1000% greater than the
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`actual value it represents), the datum cannot be considered as reliable, even
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`anecdotally. To highlight the unreliability of the data, Station 8 shows again about
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`1000% higher value (i.e., 21%) for the “Unknown” than Station 11 (i.e., 2%).
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`31.
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`In conclusion, the combination of Sampalis I, Bottino II and Randolph fails
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`to provide the claim element of “less than 3% free fatty acids” in independent
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`claims 1 and 15 and the claims dependent thereon.
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`B. Grounds 2, 3 and 4 fail because the combined references do not teach
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`each element of the claims
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`32. Rimfrost relies on Bottino II to provide the free fatty acid limitation in
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`Ground 2, 3 and 4 which are applied to claims that depend on independent claims 1
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`and 15 addressed in Ground 1. The same analysis applies to these grounds as
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`Bottino II and the references as cited against the claims do not teach the claim
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`element of “less than 3% free fatty acids.”
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`33.
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`I further declare that all statements made herein of my own knowledge are
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`true and that all statements made on information and belief are believed to be true;
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`and further that these statements were made with the knowledge that willful false
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`AKER EXHIBIT 2001 PAGE 0016
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`statements and the like so made are punishable by fine or imprisonment, or both,
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`under section 1001 of title 18 of the United States Code, and that such willful false
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`statements may jeopardize the validity of the application or any patent issued
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`thereon.
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`Respectfully submitted,
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`August 4, 2021
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`________________________
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`Dr. Jacek Jaczynski
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`AKER EXHIBIT 2001 PAGE 0017
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`APPENDIX A
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`18
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`AKER EXHIBIT 2001 PAGE 0018
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`
`Jacek Jaczynski
`West Virginia University; Davis College of Agriculture, Natural Resources, and Design
`Division of Animal & Nutritional Sciences; P.O. Box 6108, Morgantown, WV 26506-6108
`TEL: 304-293-1893; FAX: 304-293-2232; E-MAIL: Jacek.Jaczynski@mail.wvu.edu;
`
`
`Education:
`• Oregon State University, Food Science and Technology, Ph.D., 2002, dissertation: “Surimi seafood under
`thermal and e-beam processing”
`• Oregon State University, Food Science and Technology, M.S., 1998, thesis: “Antimicrobial activity of nisin
`and hen lysozyme acting in tandem against Listeria monocytogenes on a model surface”
`• Agricultural University of Poznan (Poland), Biotechnology, M.S., 1995, thesis: “Optimization of a high-cell
`density propionic acid fermentation in a continuous bio-reactor system with micro-carriers”
`
`
`Work and Teaching Experience:
`• Professor (teaching – 50%, research – 50%), West Virginia University, 2013 to present
`• Associate Professor (teaching – 50%, research – 50%), West Virginia University, 2008-2013
`• Assistant Professor (teaching – 50%, research – 50%), West Virginia University, 2002-2008
`• Graduate Research Assistant, Oregon State University Seafood Laboratory, 1998-2002
`• Graduate Research Assistant, Oregon State University, 1996-1998
`
`
`Annual Teaching:
`• HN&F 126 – Society and Food (HN&F – Human Nutrition and Food), 3 CR, fall and spring semesters,
`annual enrollment ~300, approved for General Education Foundation (GEF).
`• HN&F 126 online – Society and Food, 3 CR, summer semester available through WVU Ecampus, enrollment
`~50, approved for GEF.
`• FDST 200 – Food Science and Technology, 3 CR, fall semesters, enrollment ~100, approved for GEF.
`• FDST 200 online – Food Science and Technology, 3 CR, summer semester available through WVU Ecampus,
`enrollment ~50, approved for GEF..
`• FDST 445/545 – Food Microbiology, 3 CR, spring semesters, enrollment ~30.
`
`
`Professional Affiliations:
`• Institute of Food Technologists
`• American Chemical Society
`• World Aquaculture Society
`• Gamma Sigma Delta
`
`
`Patents and Trademarks (* – denotes primary inventor):
`• Jaczynski* J. 2010. Continuous protein and lipid recovery from food animal processing byproducts. U.S.
`Patent and Trademark Office. Patent number 7,763,717.
`• Matak KE, Jaczynski* J. 2012. YumEGGa™ - ready-to-eat egg stick snack with nutraceutical properties.
`Patent and Trademark Office. Trademark number 4,169,256.
`
`
`
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`Book Chapters (* – denotes corresponding author):
`2004
`• Jaczynski* J, Park JW. 2004. Temperature, Color and Texture Prediction Models for Surimi Seafood
`Pasteurization. In: Shahidi F, Spanier A, Ho CT, Braggins T, editors. Quality of Fresh and Processed Foods.
`New York: Kluwer Academics/Plenum Publishing. p 121-34.
`• Jaczynski* J, Park JW. 2004. Application of Electron Beam to Surimi Seafood. In: Komolprasert V,
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`AKER EXHIBIT 2001 PAGE 0019
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`Morehouse K, editors. Irradiation of Food and Packaging: Recent Developments. Washington, DC:
`American Chemical Society. p 165-79.
`2005
`• Su* YC, Daeschel MA, Frazier J, Jaczynski J. 2005. Microbiology and Pasteurization of Surimi Seafood. In:
`Park JW, editor. Surimi and Surimi Seafood, 2nd ed. Boca Raton: CRC Press. p 583-648.
`• Jaczynski* J, Hunt A, Park JW. 2005. Safety and Quality of Frozen Fish, Shellfish and Related Products. In:
`Sun DW, editor. Handbook of Frozen Food Processing and Packaging. Boca Raton: CRC Press. p 341-377.
`2007
`• Torres* JA, Chen YC, Rodrigo-García J, Jaczynski J. 2007. Recovery of By-products from Seafood
`Processing Streams. In: Shahidi F, editor. Maximizing the Value of Marine By-products. Boca Raton: CRC
`Press. p 65-90.
`2008
`• Jaczynski* J. 2008. Protein and Lipid Recovery from Food Processing By-products Using Isoelectric
`Solubilization/Precipitation. In: Papadopoulos KN, editor. Food Chemistry Research Developments.
`Hauppauge: Nova Science Publishers. p 167-198.
`2009
`• Jaczynski* J. 2009. Application of Electron Beam to Food Processing with Emphasis on Seafood Products:
`Inactivation of Food-borne Pathogens and Effects on Food Quality. In: Bellinghouse VC, editor. Food
`Processing: Methods, Techniques, and Trends. Hauppauge: Nova Science Publishers. p 211-247.
`• Jaczynski* J, Chen YC, Velazquez G, Torres JA. 2009. Procesamiento con haz de Electrones. In: Legarreta
`IG, Rosmini MA, Armenta R, editors. Tecnologia de Productos de Origen Acuatico Pescado. Mexico City:
`Editorial Limusa, S.A. de C.V. p 405-426.
`• Jaczynski* J, Chen YC, Velazquez G, Torres JA. 2009. Recuperacion de Protein as y Lipidos. In: Legarreta
`IG, Rosmini MA, Armenta R, editors. Tecnologia de Productos de Origen Acuatico Pescado. Mexico City:
`Editorial Limusa, S.A. de C.V. p 461-474.
`• Matak KE, Jaczynski* J. 2009. Food Preservation with Electron Beam. In: Hulsen I, Ohnesorge E, editors.
`Food Science Research and Technology. Hauppauge: Nova Science Publishers. p 229-246.
`2010
`• Rodrigo-García J, Jaczynski J, Torres* JA. 2010. Recovery and Utilization of Proteins from Surimi
`Processing Water. In: Bechtel PJ, Smiley S, editors. A Sustainable Future: Fish Processing Byproducts.
`Fairbanks: Alaska Sea Grant, University of Alaska. p 147-160.
`• Gehring CK, Gigliotti JC, Tou JC, Moritz JS, Jaczynski* J. 2010. The Biochemistry of Isoelectric Processing
`and Nutritional Quality of Proteins and Lipids Recovered with This Technique. In: Haugen S, Meijer S,
`editors. Handbook of Nutritional Biochemistry: Genomics, Metabolomics and Food Supply. Hauppauge:
`Nova Science Publishers. p 255-288.
`2011
`• Tahergorabi R, Hosseini SV, Jaczynski* J. 2011. Seafood Proteins. In: Phillips GO, Williams PA, editors.
`Handbook of Food Proteins. Cambridge: Woodhead Publishing Ltd. p 116-149.
`2012
`• Jaczynski* J, Tahergorabi R, Hunt A, Park JW. 2012. Safety and Quality of Frozen Aquatic Food Products.
`In: Sun DW, editor. Handbook of Frozen Food Processing and Packaging, 2nd ed. Boca Raton: CRC Press. p
`343-385.
`2013
`• Su* YC, Daeschel MA, Frazier J, Jaczynski J. 2013. Microbiology and Pasteurization of Surimi Seafood. In:
`Park JW, editor. Surimi and Surimi Seafood, 3rd ed. Boca Raton: CRC Press. p 375-410.
`2014
`• Tahergorabi R, Jaczynski J, Matak* KE. 2014. Electron Beam Inactivation of Foodborne Pathogens with an
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`AKER EXHIBIT 2001 PAGE 0020
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`Emphasis on Salmonella. In: Gomez-Lopez VM, Bhat R, editors. Practical Food Safety: Contemporary
`Issues and Future Directions. Heboken: Wiley Blackwell Publishing. p 451-471.
`• Tahergorabi R, Jaczynski* J. 2014. Isoelectric Solubilization/Precipitation as a Means to Recover Protein and
`Lipids from Seafood By-products. In: Kim SK, editor. Seafood Processing By-Products: Trends and
`Applications. New York: Springer Publishing Company. p 101-124.
`2015
`• Jaczynski* J, Tahergorabi R. 2015. Isoelectric Processing of Seafood Products: Amino Acid and Fatty Acid
`Profiles. In: Preedy VR, editor. Processing and Impact on Active Components in Food. New York: Elsevier
`Academic Press. p 417-427.
`2016
`• Tahergorabi R, Jaczynski* J. 2016. Seafood Proteins and Human Health. In: Raatz S, Bibus D, editors. Fish
`and Fish Oil in Health Promotion and Disease Prevention. New York: Elsevier Academic Press. p 323-331.
`• Tahergorabi R, Matak KE, Jaczynski* J. 2016. Inactivation Kinetics of Foodborne Pathogens with Electron
`Beam Emphasizing Salmonella. In: Jaiswal AK, editor. Food Processing Technologies: Impact on Product
`Attributes. Boca Raton: CRC Press. p 671-691.
`2017
`• Zhong T, Oporto* GS, Jaczynski J. 2017. Antimicrobial Food Packaging with Cellulose-Copper
`Nanoparticles Embedded in Thermoplastic Resin. In: Grumezescu A, editor. Food Preservation:
`Nanotechnology in the Agri-Food Industry. New York: Elsevier Academic Press. p 671-702.
`• Tahergorabi R, Jaczynski* J. 2017. Nutraceutical Egg Products. In: Hester P, editor. Egg Innovations and
`Strategies for Improvement. New York: Elsevier Academic Press. p 271-280.
`
`
`Peer-Reviewed Publications (* – denotes corresponding author and in some instances co-corresponding authors;
`impact factors and journal rankings based on 2018 Journal Citation Reports®):
`
`2002
`• Jaczynski J, Park* JW. 2002. Temperature prediction during thermal processing of surimi seafood. Journal of
`Food Science 67(8):3053-3057 (impact: 2.081, rank: 56/135).
`2003
`• Jaczynski J, Park* JW. 2003. Predictive models for microbial inactivation and texture degradation in surimi
`seafood during thermal processing. Journal of Food Science 68(3):1025-1030 (impact: 2.081, rank: 56/135).
`• Jaczynski J, Park* JW. 2003. Physicochemical properties of surimi seafood as affected by electron beam and
`heat. Journal of Food Science 68(5):1626-1630 (impact: 2.081, rank: 56/135).
`• Jaczynski J, Park* JW. 2003. Microbial inactivation and electron penetration in surimi seafood during
`electron beam processing. Journal of Food Science 68(5):1788-1792 (impact: 2.081, rank: 56/135).
`2004
`• Jaczynski J, Park* JW. 2004. Physicochemical changes in Alaska pollock surimi and surimi gel as affected by
`electron beam. Journal of Food Science 69(1):53-57 (impact: 2.081, rank: 56/135).
`2005
`• Moritz* JS, Parsons AS, Buchanan NP, Baker NJ, Jaczynski J, Gekara OJ, Bryan WB. 2005. Synthetic
`methionine and feed restriction effects on performance and meat quality of organically reared broiler
`chickens. Journal of Applied Poultry Research 14:521-535 (impact: 0.808, rank: 41/61).
`2006
`• Black JL, Jaczynski* J. 2006. Temperature effect on inactivation kinetics of Escherichia coli O157:H7 by
`electron beam in ground beef, chicken breast meat, and trout fillets. Journal of Food Science 71(6):M221-227
`(impact: 2.081, rank: 56/135).
`• Chen YC, Nguyen J, Semmens K, Beamer S, Jaczynski* J. 2006. Enhancement of omega-3 fatty acid content
`in rainbow trout (Oncorhynchus mykiss) fillets. Journal of Food Science 71(7):C383-389 (impact: 2.081,
`
`
`
`
`AKER EXHIBIT 2001 PAGE 0021
`
`
`
`rank: 56/135).
`2007
`• Chen YC, Nguyen J, Semmens K, Beamer S, Jaczynski* J. 2007. Physicochemical changes in omega-3-
`enhanced farmed rainbow trout (Oncorhynchus mykiss) muscle during refrigerated storage. Food Chemistry
`104(3):1143-1152 (impact: 5.399, rank: 7/135).
`• Chen YC, Jaczynski* J. 2007. Gelation of protein recovered from whole Antarctic krill (Euphausia superba)
`by isoelectric solubilization/precipitation as affected by functional additives. Journal of Agricultural and
`Food Chemistry 55(5):1814-1822 (impact: 3.571, rank: 28/135).
`• Tou* JC, Jaczynski J, Chen YC. 2007. Krill for human consumption: nutritional value and potential health
`benefits. Nutrition Reviews 65(2):63-77 (impact: 5.779, rank: 8/87).
`• Chen YC, Jaczynski* J. 2007. Protein recovery from rainbow trout (Oncorhynchus mykiss) processing by-
`products via isoelectric solubilization/precipitation and its gelation properties as affected by functional
`additives. Journal of Agricultural and Food Chemistry 55(22):9079-9088 (impact: 3.571, rank: 28/135).
`• Chen YC, Tou JC, Jaczynski* J. 2007. Amino acid, fatty acid, and mineral profiles of materials recovered
`from rainbow trout (Oncorhynchus mykiss) processing by-products using isoelectric
`solubilization/precipitation. Journal of Food Science 72(9):C527-535 (impact: 2.081, rank: 56/135).
`• Black JL, Jaczynski* J. 2007. Effect of ionic strength on inactivation kinetics of Escherichia coli O157:H7 by
`electron beam in ground beef, chicken breast meat, and trout fillets. International Journal of Food Science
`and Technology 42(7):894-902 (impact: 2.281, rank: 53/135).
`• Chalise PR, Hotta E, Matak KE, Jaczynski* J. 2007. Inactivation kinetics of Escherichia coli by pulsed
`electron beam. Journal of Food Science 72(7):M280-285 (impact: 2.081, rank: 56/135).
`2008
`• Black JL, Jaczynski* J. 2008. Effect of water activity on inactivation kinetics of Escherichi