AU742362B2 - Dry yeast compositions - Google Patents
Dry yeast compositions Download PDFInfo
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- AU742362B2 AU742362B2 AU71443/00A AU7144300A AU742362B2 AU 742362 B2 AU742362 B2 AU 742362B2 AU 71443/00 A AU71443/00 A AU 71443/00A AU 7144300 A AU7144300 A AU 7144300A AU 742362 B2 AU742362 B2 AU 742362B2
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- bread
- composition
- improving agent
- yeast
- dry yeast
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- 240000004808 Saccharomyces cerevisiae Species 0.000 title claims description 80
- 239000000203 mixture Substances 0.000 title claims description 37
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims description 38
- 239000003795 chemical substances by application Substances 0.000 claims description 32
- 239000008187 granular material Substances 0.000 claims description 25
- 238000000034 method Methods 0.000 claims description 21
- 102000004190 Enzymes Human genes 0.000 claims description 15
- 108090000790 Enzymes Proteins 0.000 claims description 15
- 239000002245 particle Substances 0.000 claims description 15
- 239000004382 Amylase Substances 0.000 claims description 14
- 239000000853 adhesive Substances 0.000 claims description 12
- 230000001070 adhesive effect Effects 0.000 claims description 12
- 238000000576 coating method Methods 0.000 claims description 10
- 229960005070 ascorbic acid Drugs 0.000 claims description 9
- 235000010323 ascorbic acid Nutrition 0.000 claims description 9
- 239000011668 ascorbic acid Substances 0.000 claims description 9
- 239000011248 coating agent Substances 0.000 claims description 9
- 238000000855 fermentation Methods 0.000 claims description 8
- 230000004151 fermentation Effects 0.000 claims description 8
- 238000004519 manufacturing process Methods 0.000 claims description 8
- 235000013361 beverage Nutrition 0.000 claims description 5
- 239000000725 suspension Substances 0.000 claims description 4
- 239000003925 fat Substances 0.000 claims description 3
- 235000008429 bread Nutrition 0.000 claims description 2
- 238000010348 incorporation Methods 0.000 claims description 2
- 239000007788 liquid Substances 0.000 claims description 2
- 150000003626 triacylglycerols Chemical class 0.000 claims description 2
- 229920002488 Hemicellulose Polymers 0.000 claims 1
- 239000008157 edible vegetable oil Substances 0.000 claims 1
- 241000894007 species Species 0.000 claims 1
- 235000014680 Saccharomyces cerevisiae Nutrition 0.000 description 68
- 238000002156 mixing Methods 0.000 description 24
- 229940088598 enzyme Drugs 0.000 description 15
- 108010002430 hemicellulase Proteins 0.000 description 13
- 229940059442 hemicellulase Drugs 0.000 description 12
- 230000000694 effects Effects 0.000 description 11
- ZZZCUOFIHGPKAK-UHFFFAOYSA-N D-erythro-ascorbic acid Natural products OCC1OC(=O)C(O)=C1O ZZZCUOFIHGPKAK-UHFFFAOYSA-N 0.000 description 10
- 229930003268 Vitamin C Natural products 0.000 description 10
- 235000019154 vitamin C Nutrition 0.000 description 10
- 239000011718 vitamin C Substances 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 5
- 229910052782 aluminium Inorganic materials 0.000 description 5
- 235000010210 aluminium Nutrition 0.000 description 5
- 239000004411 aluminium Substances 0.000 description 5
- 238000001035 drying Methods 0.000 description 5
- 230000002538 fungal effect Effects 0.000 description 5
- 239000003921 oil Substances 0.000 description 5
- 235000019198 oils Nutrition 0.000 description 5
- 102000003820 Lipoxygenases Human genes 0.000 description 4
- 108090000128 Lipoxygenases Proteins 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 229920002153 Hydroxypropyl cellulose Polymers 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000006071 cream Substances 0.000 description 3
- 239000000428 dust Substances 0.000 description 3
- -1 glycerol ester Chemical class 0.000 description 3
- 239000001863 hydroxypropyl cellulose Substances 0.000 description 3
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- 239000004366 Glucose oxidase Substances 0.000 description 2
- 108010015776 Glucose oxidase Proteins 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 206010020751 Hypersensitivity Diseases 0.000 description 2
- 239000004367 Lipase Substances 0.000 description 2
- 102000004882 Lipase Human genes 0.000 description 2
- 108090001060 Lipase Proteins 0.000 description 2
- 102000035195 Peptidases Human genes 0.000 description 2
- 108091005804 Peptidases Proteins 0.000 description 2
- 102000015439 Phospholipases Human genes 0.000 description 2
- 108010064785 Phospholipases Proteins 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 235000013312 flour Nutrition 0.000 description 2
- 229940116332 glucose oxidase Drugs 0.000 description 2
- 235000019420 glucose oxidase Nutrition 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 235000019421 lipase Nutrition 0.000 description 2
- 239000002265 redox agent Substances 0.000 description 2
- 108010001535 sulfhydryl oxidase Proteins 0.000 description 2
- 238000001291 vacuum drying Methods 0.000 description 2
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 1
- 101150034533 ATIC gene Proteins 0.000 description 1
- 108010059892 Cellulase Proteins 0.000 description 1
- 108010084185 Cellulases Proteins 0.000 description 1
- 102000005575 Cellulases Human genes 0.000 description 1
- 241000272194 Ciconiiformes Species 0.000 description 1
- 108010073178 Glucan 1,4-alpha-Glucosidase Proteins 0.000 description 1
- GXCLVBGFBYZDAG-UHFFFAOYSA-N N-[2-(1H-indol-3-yl)ethyl]-N-methylprop-2-en-1-amine Chemical compound CN(CCC1=CNC2=C1C=CC=C2)CC=C GXCLVBGFBYZDAG-UHFFFAOYSA-N 0.000 description 1
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- 239000005662 Paraffin oil Substances 0.000 description 1
- 235000019483 Peanut oil Nutrition 0.000 description 1
- 108090000279 Peptidyltransferases Proteins 0.000 description 1
- 239000004365 Protease Substances 0.000 description 1
- 235000019484 Rapeseed oil Nutrition 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 235000019486 Sunflower oil Nutrition 0.000 description 1
- 108090000992 Transferases Proteins 0.000 description 1
- 102000004357 Transferases Human genes 0.000 description 1
- 241000209140 Triticum Species 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 238000005273 aeration Methods 0.000 description 1
- 208000026935 allergic disease Diseases 0.000 description 1
- 230000007815 allergy Effects 0.000 description 1
- 229940025131 amylases Drugs 0.000 description 1
- 238000003556 assay Methods 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 235000015173 baked goods and baking mixes Nutrition 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 235000012180 bread and bread product Nutrition 0.000 description 1
- 108010089934 carbohydrase Proteins 0.000 description 1
- 229940106157 cellulase Drugs 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 235000005687 corn oil Nutrition 0.000 description 1
- 239000002285 corn oil Substances 0.000 description 1
- 239000002385 cottonseed oil Substances 0.000 description 1
- 235000012343 cottonseed oil Nutrition 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000007888 film coating Substances 0.000 description 1
- 238000009501 film coating Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 235000010037 flour treatment agent Nutrition 0.000 description 1
- 201000011243 gastrointestinal stromal tumor Diseases 0.000 description 1
- 239000000787 lecithin Substances 0.000 description 1
- 235000010445 lecithin Nutrition 0.000 description 1
- 229940067606 lecithin Drugs 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 235000013379 molasses Nutrition 0.000 description 1
- AYOOGWWGECJQPI-NSHDSACASA-N n-[(1s)-1-(5-fluoropyrimidin-2-yl)ethyl]-3-(3-propan-2-yloxy-1h-pyrazol-5-yl)imidazo[4,5-b]pyridin-5-amine Chemical compound N1C(OC(C)C)=CC(N2C3=NC(N[C@@H](C)C=4N=CC(F)=CN=4)=CC=C3N=C2)=N1 AYOOGWWGECJQPI-NSHDSACASA-N 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 239000000312 peanut oil Substances 0.000 description 1
- 125000001151 peptidyl group Chemical group 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 235000019833 protease Nutrition 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 238000005057 refrigeration Methods 0.000 description 1
- PPASLZSBLFJQEF-RXSVEWSESA-M sodium-L-ascorbate Chemical compound [Na+].OC[C@H](O)[C@H]1OC(=O)C(O)=C1[O-] PPASLZSBLFJQEF-RXSVEWSESA-M 0.000 description 1
- 238000005063 solubilization Methods 0.000 description 1
- 230000007928 solubilization Effects 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 239000002600 sunflower oil Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 238000011514 vinification Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 210000005253 yeast cell Anatomy 0.000 description 1
Landscapes
- Bakery Products And Manufacturing Methods Therefor (AREA)
Description
AUSTRALIA
Patents Act COMPLETE SPECIFICATION
(ORIGINAL)
Class Int. Class Application Number: Lodged: Complete Specification Lodged: Accepted: Published: Priority Related Art: Name of Applicant: DSM N.V.
Actual Inventor(s): Jan Willem Groenendaal Address for Service: PHILLIPS ORMONDE FITZPATRICK Patent and Trade Mark Attorneys 367 Collins Street Melbourne 3000 AUSTRALIA Invention Title: DRY YEAST COMPOSITIONS Our Ref: 630207 POF Code: 255815/255815 The following statement is a full description of this invention, including the best method of performing it known to applicant(s): -1- 6006q I GIST-BROCADES B.
2678S DRY YEAST COMPOSITIONS The present application is a Divisional from Australian Application 676406 (81751/94) the entire disclosure of which is incorporated herein by reference.
The present invention relates to dry yeast compositions, the production thereof and their use in bakery products and beverages.
SThe manufacture of a yeast composition starts with a 5 small sample of a pure culture. This sample is used to inoculate the first of a series of fermentations in Sfermenters of successively increasing size. The first few are mildly aerated batch fermentations. Only the last two (or sometimes three) stages are performed usina full i.10 aeration and incremental feeding of molasses. These fedbatch fermentations are carried out in fermenters having a volume of 100m 3 or more. Fermentation is typically carried out for a total of 1-20 hours during which time about 10,000-30,000 kg of compressed yeast is produced.
15 Further processing includes separating the veast f rom the broth by centrifugation and washing which results in a yeast cream (17-23% dry matter content) The yeast cream may be processed into compressed yeast (27-33% dry matter content) which is either sold as such or extruded and dried to produce active dry yeast (ADY) or instant dry yeast (IDY) with moisture contents of 6-3% and 2-8% respectively.
In the case of ADY, drying usually takes place in celt cr rotolcuvre (drum) dryers. For IDY production, fluidized-bed drying. is commonly used. Drvirn of the veast to a level of about 20% w/w water content involves only the evaporation of free water. 0Further reduction of the moisture content- requires removal of a portion of the bound water from the yeast which may cause damage to the yeast cell 2 membrane. US patents 3,843,800 and 4,248,420 describe use in such a drying process of a wetting agent such as a glycerol ester and/or fatty acid ester of propylene glycol so as to preserve the desired high direct leavening activity of the yeast.
Dry yeast loses' part of its leavening activity during both drying and rehydration. Dry yeasts are still commonly used in the bakery trade because of their extended stability and because refrigeration is unnecessary. Dry yeasts are used in wine making to obtain a fast and reproducible fermentation thereby avoiding the risk of Sfailure of natural fermentation. Moreover, the yeast is immediately available throughout the year.
Instant dry yeast (IDY) is the latest type of baker's yeast, which was introduced in the early 1970s (see *.e for example US patent 3,843,800) This was followed a few years later by introduction of instant dry wine yeast (IWY) which can be regarded as a special form of instant dry yeast. To obtain a high quality IDY, compressed yeast of relatively high protein content (42-60% must be dried in a aqick drying process. The leavening activity of IDY under conditions of application is about 75-85% that of compressed yeast. The shelf life in a vacuum-sealed package is comparable to that of ADY.
IDY is presented typically in the form of very small rods that are highly porous and easy to rehvdrate. On the one hand, this allows immediate use, without prior rehydration. On the other hand, the high porosity gives easy access to water and oxygen (from air) which results in a rather rapid loss of activity upon exposure to atmospheric conditions. For satisfactory results, IDY should be used within 3- days of opening the package. Moreover, the hich porosity of IDY makes it sensitive to extreme rehydraticn conditions.
3 5 IDY usually has a moisture content of 2-8% and a protein content between 42 and 60% on a dry matter basis.
3 In baking, besides bakers' yeast, processing aids such as bread improvers are used, including oxidising and reducing agents, enzymes such as redox enzymes, a-amylases, amyloglucosidases, hemicellulases, cellulases and proteases, s lipases and phospholipases, emulsifiers and fatty materials.
Yeast, enzymes and redox agents are added separately to doughs. Yeast may be added in cream, compressed, active dry or instant dry form. Enzymes may be added in dry powder or in dissolved form. Redox agents are in most cases used in io powder form.
Separate weighing and dosing of these various ingredients increases the number of actions which have to be performed by the operators of the production process.
Inherent in this increased number of actions is a greater is chance of introducing errors resulting in negative impact on the quality of the end product. Moreover, working with dusty materials may initiate allergic reactions.
Mixing of ingredients with dry granular yeast or instant dry yeast may result in homogeneous oroducts 20 directly after mixing. However, during transcort and storage prior to use, this type of product tends to lose homogeneity (see Example To solve these problems various solutions have been proposed.
J-73040748 describes the mixing of granular semi-dry yeast (moisture content of 35-45% w/w) with a wheat flour improving agent for use in breadmaking. In such a mnx-ur the stability of both the flour improving agent and yeast is very limited due to the high water contenc. Thus, scecial attention has to be paid to storage and transport conditions.
DE-2515029 describes the production of active dry yeast by vacuum drying and coformulation of the dry yeast with spray dried malt extract or maltodextri.s. Malt excract or maltodexrins are added as a dewaterina agent. However, this vacuum drying technique cannon be applied economically on a commercial scale due to unacceptable loss in leavening activity. In general, a yeast composition produced by this technique will in powder or dust form, which may result in allergy.
The above discussion of documents, acts, materials, devices, articles and the like is included in this specification solely for the purpose of providing a context for the present invention. It is not suggested or represented that any or all of these matters formed part of the prior art base or were common general knowledge in the field relevant to the present invention as it existed in Australia before the priority date of each claim of this application.
The present invention provides a dry yeast composition which has the advantage of provision of dry yeast with a bread-improving agent, but which has none of the above-mentioned disadvantages such as dust formation and loss of homogeneity of the composition during transport.
Thus in one aspect the present invention provides a dry granular yeast 15 composition having a moisture content of not more than about 8% and containing about 0.1 to 8% of a bread improving agent, wherein the dry yeast is present in granular form and wherein the bread-improving agent includes one or more enzymes and/or ascorbic acid, and wherein said breadimproving agent is present in a form selected from 20 a granulate having substantially the same granula size as the dry yeast, and a coating on the dry yeast granules in the form of a film or adhered particles.
In principle, a dry yeast composition of the present invention may have substantially the same granule size or not a greatly increased granule size compared to the starting dry yeast before the bread-improving agent is added.
Additionally, a composition of the invention has the same convenience of use as dry yeast, which makes application possible without adapting operational procedures or equipment.
Preferably, the bread-improving agent is added to the dry yeast at 1 to 4% Enzymes for this purpose can be selected from carbohydrases such a a-amylase, ayloglucosidase, hemicellulase, cellulase and glucanase, protein modifying enzymes such as proteses and peptidases, redox enzymes such as glucose oxidase, sulfhydryloxidase and lipoxidase (lipoxygenase), peptidyl W:Connie\oAVID\6764O8 sped (page 4).doc 4 A enzymes such as glucose oxidase, sulfhydryloxidase and lipoxidase (lipoxygenase), peptidyl transferases such as y-glutamyl transferase and lipid modifying -enzymes such as lipases and phospholipases.
DocumentO 5 In one embodiment of the invention, the breadimproving agent is present as a granulate having substantially the same granule size as the dry yeast. Where the bread-improving agent comprises more than one component, the components may be produced together as a homogeneous granular form or each component may be produced separately in granular form. The latter is especially preferred since this enables the ratio of the components of the breadimproving agent to be varied prior to mixing with the dry yeast. Mixing of the bread-improving agent and the dry yeast can be carried out using conventional mixing methods. Any known mixing method can be applied, provided attention is paid to preventing substantial damage to the granules, which Smay lead to loss of activity or dust formation.
n another embodiment of the invention, the breadimproving agent is coated on to the dry yeast granules. The coating may be in the form of very small adhered particles or a film. If a bread-imcroving agent is emplcyed to provide a particle coating, preferably at least 50% of the particles 2.0 will have a size smaller than 50urm. It has been found advantageous for at least 80% of the particles to have a smaller size than 50am. Particles of a bread-im;roving agent which are too large for direct use in a comcsiticn of the invention -can be reduced to appropriate size using suitable ecuipment known in the art such as a milling apparatus.
The bread-improving agent particles are stuck on to the dry yeast using suitable adhesives. These will be in general focdgrade adhesives, preferably have a keeing cuality of at least two years when applied on dry yeast and ?0 will not influence the taste or flavour of the dry yeast, the dough prepared with the yeast or the final bread product. The adhesive is preferab a dded to a mixture cf yeast granules and microfine bread-improving particles, e.g.
at 0.5 to 1.0% During application of the adhesive, continuous mixing is preferably carried out. The adhesive is preferably slowly supplied either continucusly or batch-wise using small portions each time. After completion of addition 6 of the adhesive, the mixing will continue until substantially all the bread-improving particles are stuck on to the dry yeast granules. While the adhesive can be poured on to the mixture, preferably the adhesive is sprayed on to the mixture to obtain a more uniform distribution. An inline mixing process may be used (see Example 6) Suitable adhesives are e.g. oils such as soy oil, cotton seed oil, rape seed oil, sunflower oil, corn oil, peanut oil, olive oil, paraffin oil, triglycerides, liquid io fats and mixtures thereof. Fractionated oils can be used.
The adhesive may include one or more additives which are beneficial in improving the sticking characteristics.
Thus, for example, lecithin may be advantageously mixed with soy oil.
For formation of dry yeast granules with a film coating of a bread-improving agent, the bread-improving agent will be prepared in the form of a suspension or solution. Subsecuently, the suspension or solution will be coated cn to the dry yeast granules by using coating 20 apparatus known per se, e.g. a fluidized bed or coating pan.
Excess water will be removed so as to provide a dry film of bread-improving agent around each dry yeast granule. A binding agent may be advantageously added to the suspension or solution of the bread-improving agent to promote binding to the yeast granules, e.g. hydroxypropyl cellulose.
In further aspects, the present invention additionally provides use of a dry granular yeast composition of the invention for incorporation into a dough or for fermentation of a beverage and doughs and beverage compositions incorporating such a dry yeast composition.
7 The following examples illustrate the invention.
Example 1 (comparative example) 2,700 g Fermipan T M (dry yeast of Gist-brocades) were s homogeneously mixed with 36 g ascorbic acid, 6 g fungal aamylase Fermizyme T
P
2 00 (Gist-brocades, 4740 PU/g) and 48g hemicellulase Fermizyme T
H
1000 (Gist-brocades, hemicellulase activity 13,500 HUJ/g and a-amylase activity 942 PU/g) in a Hobart mixer. Directly after mixing, portions of 450 g were io weighed and packed in aluminium bags, which were closed at reduced pressure.
The homogeneity of the contents of three packs was tested directly after packing by opening each pack at three places, near the top, in the middle, and near the bottom, and withdrawing samples of 25 g from each opening. In these samples, the levels of ascorbic acid, fungal a-amylase and hemicellulase were analyzed according to the following methods: ascorbic acid analysis was carried out 20 according to the conventional method of Boehringer.
fungal c-amylase activity was determined using PhadebasT tablets from Pharmacia. In this method, solubilization of dye-labelled starch by c-amylase over minutes in a buffer at pH 5.5 and 30'C is measured spectrophotometrically. e-amylase activity is expressed in Phadebas Units (PU) using an Asoeraillus orvzae fungal camylase preparation of 10,000 PU/g as an internal standard.
One Phadebas Unit defined in this way equals about 10 SKB units, used in the baking industry.
fungal hemicellulase activity was determined by measuring the amount of reducing sugars produced over a predetermined ti.e period in the micro-assay as described by Leathers Kurtzman, C.P. and Detroy, R.W. in Biotechnol. Bioeng. Symp., (1984) j14, 225. In this paper, the hemicellulase unit (HU) is also defined.
The results are summarised in Table 1.
8 Another three packs prepared as described above were stored for two weeks in a refrigerator at 4-C. Afterwards, these packs were placed in a conventional carton for instant yeast packs and surrounded by conventional instant yeast packs. This case was transported by a heavy goods vehicle over about 2500 kmc such that the packs were in a vertical position. Afterwards, the three test packs were stored in a refrigerator again for another four weeks. The homogeneity was then tested in the above described way. The analysis o0 results are summarised in Table 1.
0 000 *000 00.0.
0 0 *0 0 TABLE 1 Homogeneous mi> Top ascorbic acid I a-amylase hemicellulase :Middle ascorbic acid a-amylase SIhemicellulase Relative Amount recovered directly after transport 0.013 g/g 1015 85.2 256 U/g 93.5 9 A 232 HU/g 100.8 92.5 0.013 g/g 102.0 89.2 26 PU/g 98.1 94.6 232 HU/g 99.6 91.4 Bottom ascorbic acid 0.013 g/g c-amylase hemicellu 26 PU/g 99.1 112.3 101.7 108.6 93.7 106.9 lase 232 HU/g From these results, it is clear that during storage and transport, the mixture of yeast, ascorbic acid and enzymes lost hcmogeneity.
9 Example 2 Mixing process for 1 kg dry yeast composition a) The following components were weighed: Fermipan TM (dry yeast of Gist-brocades having dry matter content of Vitamin C microfine Hemicellulase 25,690 HU/g a-amylase 11,400 PU/g Kriskol 3000 (fractionated fat, Loders, Croklaan) 975.700g+97.57% 16.873g= 1.69% 0.856g= 0.08% 1.632g= 0.16% 5,000q= 0.50% 1,000g 100% Ge
C
rc..
Cc
CC...
Cc
C
C
S.
*c C b) A premix was prepared consisting of 100 g Fermipan TM combined with the total amount of vitamin C and enzymes by mixing the components with a spoon in a 250ml beaker.
c) The premix was put in the mixing beaker of a Hobart planetary mixer together with the remaining part of the Fermipan.
d) Mixing was started and the Kriskol 3000 was added in 30 sec.
The total mixing time was 10 mins.
e) The final product was vacuum packed in aluminium bags and stored at 5 OC.
Document7 10 006* .0 00060 ,go.
0000 Example 3 mixing process for 30 kg dry yeast composition a) The following components were weighed: Fernipan TI 29,121 g =97.07% vitamin C microfine 505.2 g 1.69 Hemicellulase. 25,690 HTJ/g 25.7 g 0.08% a-amylase 11,400 PtJ/g 49.0 g 0.16 Durkex 500 (mixture of soy 300 g 1.00 oil and cotUton seed oil, Otto Aldag, Hamburg 30,000 g 100% b) A premix was precared by combininq ,37 -TM t_ O a Ferm-i ina n th -oa amount of Vitamin C and enzym,.es and 15 99g of DurkIex 500 i. n a Hobart OplanetarV mixer.
c) The premix was put in a Nauta conicalmie together with the remaining part. off the FermiroDn.
d) Mixing was started and the remaining part of the Durkex 500 was added in 40 sec. The total mixing tim..e Was 10 Minls.
a) The f--inal pDroduct was vacuum packecd .n alu-minium bags and stored at 11 Example 4 Granulating process for 500 kg of Vitamin C and enzymes prepared in a Multi-Stage spray-dryer and mixing process to produce 10,000 kg of dry yeast composition.
a) The following components were weighed: Vitamin C 15.6 kg 3.12% Vitamin C sodium 420.2 kg 84.04% .2 k Hemicellulase 25,690 HU/g 22.1 kg 4.42% 10 c-amylase 11,400 PU/g 42.1 kg 8.42% 500 kg 100 water 750 kg 15 b) A solution was prepared by mixing the Vitamin C and enzymes with the water in a vessel of 1500 1 equipped with a turbine stirrer.
c) Directly after preparation of the solution, it was fed to a Stork Multi-Stage spray-dryer and dried with fine return at an inlet temperature of about 160'C and an outlet temperature of about d) 197 kg of the MSD-granulate was transported to a conical Nauta mixer with a capacity of 15 m 3 together with 9,303 kg of Fermipan'. The total mixing time was 20 mins.
e) The dried product was vacuum packed in aluminium bags and stored at 12 Example Coating process for 5 kg dry yeast composition a) The following components were weighed: Fermipan, 4,803.5 g 96.7 Vitamin C microfine 3 g 0.06 -Vitamin C sodium 81.4 g 1.63 Hemicellulase 25,690 HU/g 4.3 g 0.08 a-amylase 11,400 PU/g 8.2 g 0.16 io hydroxypropyl cellulose 100 g 2.00 5,000 g 100 b) A solution was prepared by mixing the Vitamin C, enzymes and hydroxypropyl cellulose with the water in a 3 c) Directly after the preparation of the solution, it was fed at a rate of about 15 g per min to an Aeromatic MG-1 fluidized bed coating apparatus equipped with a Wurster column containing the Fermipan The inlet temperature was about 75'C and the outlet temperature about d) The dried product was vacuum packed in aluminium bags and stored at 13 Exa-mple 6 In-line mixing process for 10,000 kg dry yeast composition a) The following components-were weighed: FermipanL' 9,706.4 kg vitamin C microfine 168.7 kg Hemicellulase 25,690 l{U/g 8.6 kg a-amnylase 11,400 PIJ/g 16.3 kg Durkex 500 100 ka 10,000 kg 97.07 1.69 0.08 0.2.6 1.00% 100 0%.
0*0.
0 0 b) A Premix was pre-pared of 1,456 kg oFf Fermipan TI combined with the total a-mount off Vitam.in C and enzymtes and 33 kg off the Durkex 500 in a Nauta conical 15 mixer. The -,mi:4ing time was 20 mins.
C) This premix was fed with the aid off Oneur.atic transport to an in-line mixer together wit-, the remaining part off the Fermioan T'and the remaining part of thne Durkex 500. The flow off Fermipan, the premiix and th uke 0 were adjusted to accord with the above-menticned comoiositzion with the aid off automatic dosing units.
d) D-irectly following the in-line mix<er, the product was vacuum packed in aluminiLum bas and stored at
Claims (12)
1. A dry granular yeast composition having a moisture content of not more than about 8% and containing about 0.1 to 8% of a bread-improving agent, wherein the dry yeast and the bread-improving agent is present in granular form, and wherein the bread-improving agent includes one or more enzymes and/or ascorbic acid, and wherein said bread-improving agent present in a form selected from a granulate having substantially the same granule size as the dry 10 yeast; and a coating on the dry yeast granules in the form of a film or adhered particles. .o
2. A composition as claimed in claim 1 wherein said bread-improving agent is 15 present as adhered particles on the dry yeast granules, at least 50%, preferably at least 80%, of said adhered particles having a diameter of less then
3. A composition as claimed in claim 1 or 2 wherein said bread-improving agent is present in the form of particles adhered to the dry yeast granules by 20 means of an adhesive comprising one or more of edible oils, triglycerides and liquid fats.
4. A composition as claimed in claim 3 wherein the bread-improving agent includes at least one of a hemicellulose and an ca-amylase.
A process for the production of a composition as claimed in claim 1 wherein a bread improving agent in granular form is mixed with granules of dry yeast having a moisture-content of not more than about 8%
6. A process for the production of a composition as claimed in claim 1 or claim 2 wherein dry yeast granules having a moisture content of not more than about 8% are mixed with smaller particles of a bread-improving agent in the C: WINWORD'MICHELLEODELETE SPECIES,87641DOC presence of an adhesive so that said yeast granules become coated with particles of the bread-improving agent.
7. A process for the production of a composition as claimed in claim 1 wherein a suspension or a solution of the bread-improving agent is coated onto dry yeast granules having a moisture content of not more than about 8% (w/w) followed by removal of excess moisture.
8. A process as claimed in claim 7 wherein coating of the yeast granules is 10 carried out by a fluidized bed process or a coating pan process.
9. Use of a composition as claimed in any one of claims 1 to 4 for incorporation into a dough or for fermentation of a beverage. 15
10. A dough or beverage composition incorporating a composition as claimed in any one of claims 1 to 4. i
11. A composition according to claim 1 substantially as hereinbefore described with reference to the examples 2 to 6.
12. A process according to any one of claims 5 to 8 substantially as hereinbefore described with reference to examples 2 to 6. DATED: 6 November 2000 PHILLIPS ORMONDE FITZPATRICK Attorneys for: DSM N.V. C:AWINWOROWICIIELLE OOELETCSPECIESeor DOC
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU71443/00A AU742362B2 (en) | 1993-12-24 | 2000-11-06 | Dry yeast compositions |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP93203697 | 1993-12-24 | ||
| AU71443/00A AU742362B2 (en) | 1993-12-24 | 2000-11-06 | Dry yeast compositions |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU81731/94A Division AU676406C (en) | 1993-12-24 | 1994-12-23 | Dry yeast compositions |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU7144300A AU7144300A (en) | 2001-02-08 |
| AU742362B2 true AU742362B2 (en) | 2002-01-03 |
Family
ID=3754309
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU71443/00A Ceased AU742362B2 (en) | 1993-12-24 | 2000-11-06 | Dry yeast compositions |
Country Status (1)
| Country | Link |
|---|---|
| AU (1) | AU742362B2 (en) |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1509676A (en) * | 1967-01-30 | 1968-01-12 | Process for manufacturing activated nutritional yeast | |
| US3959494A (en) * | 1973-06-22 | 1976-05-25 | The Distillers Company (Yeast) Limited | Active dried yeast composition |
-
2000
- 2000-11-06 AU AU71443/00A patent/AU742362B2/en not_active Ceased
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1509676A (en) * | 1967-01-30 | 1968-01-12 | Process for manufacturing activated nutritional yeast | |
| US3959494A (en) * | 1973-06-22 | 1976-05-25 | The Distillers Company (Yeast) Limited | Active dried yeast composition |
Also Published As
| Publication number | Publication date |
|---|---|
| AU7144300A (en) | 2001-02-08 |
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| PC1 | Assignment before grant (sect. 113) |
Owner name: DSM IP ASSETS B.V. Free format text: THE FORMER OWNER WAS: DSM N.V. |
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| CH | Opposition withdrawn |
Opponent name: BURNS PHILP TECHNOLOGY AND DEVELOPMENT PTY LTD |
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| FGA | Letters patent sealed or granted (standard patent) |