Abstract: Aspects of the disclosure relate to an article carrier (90; 290; 490) for packaging one or more articles and to a blank (10; 110; 210; 310; 410) for forming the carrier. The carrier comprises a main panel (12; 112; 212, 222; 312, 322A, 322B; 412, 422A, 422B) including an article retention structure (RT; RT1, RT2) having an article receiving opening defined in part by at least a pair of opposing engaging tabs (40, 42; 140, 142; 240, 242, 246, 248; 340, 342, 346, 348; 440, 442, 446, 448) each having a length (L1, L2) greater than a half of the distance (L3) between their hinged connections (13A, 41; 213, 215, 241, 247, 249; 313, 315, 341, 347, 349; 413, 415, 441, 447, 449) to the main panel (12; 112; 212, 222; 312, 322A, 322B; 412, 422A, 422B).

Abstract: Disclosed herein are genetically engineered amylase enzymes, compositions including the enzymes, and methods of making and using the enzymes or compositions including the enzymes.

Abstract: A top engaging carrier (90; 190) comprises an engaging panel (12; 112) with at least one article retention structure (RT1, RT2). The article retention structure (RT1, RT2) comprises a plurality of tabs (40, 42, 44, 46, 70, 72, 74, 76; 140, 142, 144, 146, 170, 172, 174, 176; 240, 246, 276; 340, 346, 376) disposed about an article receiving aperture (A1, A2). The plurality of tabs comprises a first pair of article-engaging tabs (40, 46; 140, 146; 240, 246; 340, 346) separated by a separation element. The separation element extends from the aperture toward a corner of the engaging panel (12; 112). The corner is defined by an intersection between a first fold line (13, 15; 113A, 115A; 213, 215; 313A, 315A), hingedly connecting an end panel (14, 16; 114A/114B, 116A/116B) to the engaging panel (12; 112), and a second fold line (17, 19; 117A, 119A; 217, 219; 317A, 319A), hingedly connecting a side panel (18, 20; 118A/118B, 120A/120B) to the engaging panel (12; 112).

Abstract: Aspects of the disclosure relate to a package, an article carrier (90; 190; 290; 390; 490) for packaging one or more articles (B) and a blank (10; 110; 210; 310; 410) for forming the carrier. The article carrier (90; 190; 290; 390; 490) comprising a top panel (12; 112; 212; 312; 412) and a skirt structure surrounding and extending from the top panel (12; 112; 212; 312; 412). The skirt structure comprises a plurality of panels (14, 16, 18, 20, 24A, 24B, 28A, 28B; 114A, 114B, 116A, 116B, 118A, 118B, 120A, 120B, 124A, 124B, 128A, 128B; 214, 216, 218, 220; 314, 316, 318, 320, 324A, 324B, 328A, 328B; 414A, 414B, 416A, 416B, 418A, 418B, 420A, 420B, 424A, 424B, 428A, 428B) which include at least a first pair of opposing panels (PA1, PB1, PA2, PB2).

Abstract: Aspects of the disclosure relate to an article carrier (90; 290; 490) for packaging one or more articles and to a blank (10; 110; 210; 310; 410) for forming the carrier. The carrier comprises a main panel (12; 112; 212, 222; 312, 322A, 322B; 412, 422A, 422B) including an article retention structure (RT; RT1, RT2) having an article receiving opening defined in part by at least a pair of opposing engaging tabs (40, 42; 140, 142; 240, 242, 246, 248; 340, 342, 346, 348; 440, 442, 446, 448) each having a length (L1, L2) greater than a half of the distance (L3) between their hinged connections (13A, 41; 213, 215, 241, 247, 249; 313, 315, 341, 347, 349; 413, 415, 441, 447, 449) to the main panel (12; 112; 212, 222; 312, 322A, 322B; 412, 422A, 422B).

Abstract: A product container includes a first compartment, including a first-compartment first edge, a second compartment, including a second-compartment first edge, and a hinged connection extending between the first-compartment first edge and the second-compartment first edge. The second compartment is pivotable about the hinged connection relative to the first compartment to convert the product container between a closed state and an open state. In the closed state, the first compartment and the second compartment are in a stacked configuration. In the open state, the first compartment and the second compartment are in a side-by-side configuration.

Abstract: A packaging system includes a container defining an internal volume. The container includes a container body and a lid hingedly connected to the container body. The packaging system further includes a dunnage panel received in the internal volume of the container. The dunnage panel includes a plurality of discontinuous lines of weakness.

Abstract: The invention provides hydrolases, polynucleotides encoding them, and methods of making and using these polynucleotides and polypeptides. In one aspect, the invention is directed to polypeptides, e.g., enzymes, having a hydrolase activity, e.g., an esterase, acylase, lipase, phospholipase (e.g., phospholipase A, B, C and D activity, patatin activity, lipid acyl hydrolase (LAH) activity) or protease activity, including thermostable and thermotolerant hydrolase activity, and polynucleotides encoding these enzymes, and making and using these polynucleotides and polypeptides. The hydrolase activities of the polypeptides and peptides of the invention include esterase activity, lipase activity (hydrolysis of lipids), acidolysis reactions (to replace an esterified fatty acid with a free fatty acid), transesterification reactions (exchange of fatty acids between triglycerides), ester synthesis, ester interchange reactions, phospholipase activity and protease activity (hydrolysis of peptide bonds).

Abstract: Provided are hydrolases, including lipases, saturases, palmitases and/or stearatases, and polynucleotides encoding them, and methods of making and using these polynucleotides and polypeptides. Further provided are polypeptides, e.g., enzymes, having a hydrolase activity, e.g., lipases, saturases, palmitases and/or stearatases and methods for preparing low saturate or low trans fat oils, such as low saturate or low trans fat animal or vegetable oils, e.g., soy or canola oils.

Abstract: In alternative embodiments, the invention provides phosphatidylinositol-specific phospholipase C (PI-PLC) enzymes, nucleic acids encoding them, antibodies that bind specifically to them, and methods for making and using them. Industrial methods and products comprising use of these phospholipases are also provided. In certain embodiments, provided herein are methods for hydration of non hydratable phospholipids (NHPs) within a lipid matrix. The methods enable migration of NHPs to an oil-water interface thereby allowing the NHPs to be reacted and/or removed from the lipids. In certain embodiments, provided is a method for removing NHPs, hydratable phospholipids, and lecithins from vegetable oils to produce a degummed oil or fat product that can be used for food production and/or non-food applications. In certain embodiments, provided herein are methods for hydration of NHPs followed by enzymatic treatment and removal of various phospholipids and lecithins.

Abstract: Provided are hydrolases, including lipases, saturases, palmitases and/or stearatases, and polynucleotides encoding them, and methods of making and using these polynucleotides and polypeptides. Further provided are polypeptides, e.g., enzymes, having a hydrolase activity, e.g., lipases, saturases, palmitases and/or stearatases and methods for preparing low saturate or low trans fat oils, such as low saturate or low trans fat animal or vegetable oils, e.g., soy or canola oils.

Abstract: The invention provides hydrolases, polynucleotides encoding them, and methods of making and using these polynucleotides and polypeptides. In one aspect, the invention is directed to polypeptides, e.g., enzymes, having a hydrolase activity, e.g., an esterase, acylase, lipase, phospholipase (e.g., phospholipase A, B, C and D activity, patatin activity, lipid acyl hydrolase (LAH) activity) or protease activity, including thermostable and thermotolerant hydrolase activity, and polynucleotides encoding these enzymes, and making and using these polynucleotides and polypeptides. The hydrolase activities of the polypeptides and peptides of the invention include esterase activity, lipase activity (hydrolysis of lipids), acidolysis reactions (to replace an esterified fatty acid with a free fatty acid), transesterification reactions (exchange of fatty acids between triglycerides), ester synthesis, ester interchange reactions, phospholipase activity and protease activity (hydrolysis of peptide bonds).

Abstract: Provided are hydrolases, including lipases, saturases, palmitases and/or stearatases, and polynucleotides encoding them, and methods of making and using these polynucleotides and polypeptides. Further provided are polypeptides, e.g., enzymes, having a hydrolase activity, e.g., lipases, saturases, palmitases and/or stearatases and methods for preparing low saturate or low trans fat oils, such as low saturate or low trans fat animal or vegetable oils, e.g., soy or canola oils.

Abstract: The invention provides hydrolases, polynucleotides encoding them, and methods of making and using these polynucleotides and polypeptides. In one aspect, the invention is directed to polypeptides, e.g., enzymes, having a hydrolase activity, e.g., an esterase, acylase, lipase, phospholipase (e.g., phospholipase A, B, C and D activity, patatin activity, lipid acyl hydrolase (LAH) activity) or protease activity, including thermostable and thermotolerant hydrolase activity, and polynucleotides encoding these enzymes, and making and using these polynucleotides and polypeptides. The hydrolase activities of the polypeptides and peptides of the invention include esterase activity, lipase activity (hydrolysis of lipids), acidolysis reactions (to replace an esterified fatty acid with a free fatty acid), transesterification reactions (exchange of fatty acids between triglycerides), ester synthesis, ester interchange reactions, phospholipase activity and protease activity (hydrolysis of peptide bonds).

Abstract: In alternative embodiments, the invention provides phosphatidylinositol-specific phospholipase C (PI-PLC) enzymes, nucleic acids encoding them, antibodies that bind specifically to them, and methods for making and using them. Industrial methods and products comprising use of these phospholipases are also provided. In certain embodiments, provided herein are methods for hydration of non hydratable phospholipids (NHPs) within a lipid matrix. The methods enable migration of NHPs to an oil-water interface thereby allowing the NHPs to be reacted and/or removed from the lipids. In certain embodiments, provided is a method for removing NHPs, hydratable phospholipids, and lecithins from vegetable oils to produce a degummed oil or fat product that can be used for food production and/or non-food applications. In certain embodiments, provided herein are methods for hydration of NHPs followed by enzymatic treatment and removal of various phospholipids and lecithins.

Abstract: In alternative embodiments, the invention provides phosphatidylinositol-specific phospholipase C (PI-PLC) enzymes, nucleic acids encoding them, antibodies that bind specifically to them, and methods for making and using them. Industrial methods and products comprising use of these phospholipases are also provided. In certain embodiments, provided herein are methods for hydration of non hydratable phospholipids (NHPs) within a lipid matrix. The methods enable migration of NHPs to an oil-water interface thereby allowing the NHPs to be reacted and/or removed from the lipids. In certain embodiments, provided is a method for removing NHPs, hydratable phospholipids, and lecithins from vegetable oils to produce a degummed oil or fat product that can be used for food production and/or non-food applications. In certain embodiments, provided herein are methods for hydration of NHPs followed by enzymatic treatment and removal of various phospholipids and lecithins.

Abstract: The invention provides hydrolases, polynucleotides encoding them, and methods of making and using these polynucleotides and polypeptides. In one aspect, the invention is directed to polypeptides, e.g., enzymes, having a hydrolase activity, e.g., an esterase, acylase, lipase, phospholipase (e.g., phospholipase A, B, C and D activity, patatin activity, lipid acyl hydrolase (LAH) activity) or protease activity, including thermostable and thermotolerant hydrolase activity, and polynucleotides encoding these enzymes, and making and using these polynucleotides and polypeptides. The hydrolase activities of the polypeptides and peptides of the invention include esterase activity, lipase activity (hydrolysis of lipids), acidolysis reactions (to replace an esterified fatty acid with a free fatty acid), transesterification reactions (exchange of fatty acids between triglycerides), ester synthesis, ester interchange reactions, phospholipase activity and protease activity (hydrolysis of peptide bonds).

Abstract: The invention provides novel methods for making or modifying oils, e.g., plant, animal or microbial oils, such as vegetable oils or related compounds, that are low in a particular fatty acid(s), for example, low linoleic oils, low linolenic oils, low palmitic oils, low stearic oils or oils low in a combination thereof.

Abstract: Provided are hydrolases, including lipases, saturases, palmitases and/or stearatases, and polynucleotides encoding them, and methods of making and using these polynucleotides and polypeptides. Further provided are polypeptides, e.g., enzymes, having a hydrolase activity, e.g., lipases, saturases, palmitases and/or stearatases and methods for preparing low saturate or low trans fat oils, such as low saturate or low trans fat animal or vegetable oils, e.g., soy or canola oils.

Abstract: Provided are hydrolases, including lipases, saturases, palmitases and/or stearatases, and polynucleotides encoding them, and methods of making and using these polynucleotides and polypeptides. Further provided are polypeptides, e.g., enzymes, having a hydrolase activity, e.g., lipases, saturases, palmitases and/or stearatases and methods for preparing low saturate or low trans fat oils, such as low saturate or low trans fat animal or vegetable oils, e.g., soy or canola oils.