Reduced fat sour cream

Information

  • Patent Grant
  • 5096730
  • Patent Number
    5,096,730
  • Date Filed
    Friday, August 17, 1990
    34 years ago
  • Date Issued
    Tuesday, March 17, 1992
    32 years ago
Abstract
The present invention provides sour cream formulated with microparticulated protein which serves as a replacement for all or part of the fat and/or oil normally found in sour cream.
Description

BACKGROUND
The present invention relates to reduced fat sour cream compositions which include a microparticulated protein product as described in our allowed U.S. Pat. No. 4,961,953, the entire disclosure of which is incorportated by reference herein.
SUMMARY OF THE INVENTION
The present invention is a reduced fat sour cream having all or part of the fat and/or oil content normally found in sour cream replaced with a proteinaceous, water-dispersible, macrocolloid comprising substantially non-aggregated particles of denatured protein having in a dry state a mean diameter particle size distribution ranging from about 0.1 to about 2.0 microns, with less than about 2 percent of the total number of particles exceeding 3.0 microns in diameter, and wherein the majority of the said particles are generally spheroidal as viewed at about 800 power magnification under a standard light microscope, the particles in a hydrated state form said macrocolloid having substantially smooth, emulsion-like organoleptic character.





BRIEF DESCRIPTION OF THE DRAWING
FIG. 1 illustrates a photomicrographic view at 1000x magnification of a sample of microparticulated whey protein according to the present invention.





DETAILED DESCRIPTION OF THE INVENTION
The following examples relate to preferred methods and procedures for practicing the present invention. Example 1 relates to a preferred method for the production of microparticulated protein from the proteinaceous material present in acidified whey. Example 2 relates to a preferred method for the production of microparticulated protein from casein micelles and the proteinaceous material present in egg white. Example 3 relates to the production of microparticulated protein from the proteinaceous material in whey. Example 4 relates to the preparation of a reduced fat sour cream. Example 5 relates to the preparation of a flavored reduced fat sour cream dip.
EXAMPLE 1
Microparticulated Protein Produced from Acidified Whey
Microbiologically, aromatically and particulately clean water produced by a reverse osmosis process is added to a sanitary tank.
Commercially available liquid whey protein concentrate is treated by ultrafiltration and evaporation until the concentration of protein is about 50-55% by weight, on a dry basis. The whey protein concentrate is added to the water in the sanitary tank with agitation avoiding aeration through the suction side of a positive displacement pump to achieve a solids concentration of about 37% solids for the mixture.
As this mixture is recirculated back to the sanitary tank, a dilute solution of food acid (acetic, lactic, citric or hydrochloric: alone or in combination) is added through an in-line mixer to lower the pH from about 6.8 to about 4.4.+-.0.05.
The pH adjusted mixture is then rigorously deaerated in a Versator deaerator/homogenizer and bottom fed into a holding tank which is equipped for non-aerating agitation.
The deaerated mix is then pumped (300 lbs/hr) from the holding tank, by a positive displacement pump through an in-line strainer (300 .mu.m cheesecloth) and a mass flow meter, into a plate heat exchanger which heats the mixture to about 165.degree.-180.degree. F., a temperature lower than the target peak temperature which is achieved within a heat and shear generating apparatus ("microcooker"). Flow is manually-controlled based on readings from the in-line flow-meter.
The heated mixture is pumped directly from the plate heat exchanger into the microcooker apparatus as described in U.S. Pat. No. 4,823,396 with the exception that the inlet and outlet ports have been interchanged or exchanged, i.e., the inlet port is disposed where the outlet port is shown in the patent drawing and the outlet port is located at the bottom of the bowl shaped vessel and the temperature of the mixture is raised to about 200.degree. F. within less than 10 seconds under high shear conditions. Rigorous temperature control of the mixture is maintained at 200.degree. F. by means of a cascade control loop. The control loop senses the temperature of the product exiting the microcooker and maintains it at 200.degree. F. by adjusting the temperature of the mixture leaving the plate heat exchanger.
The speed of the rotor in the microcooker is held constant, for example, at about 3715 rpm. At this rpm, the shear rate is about 27,000 reciprocal seconds at the tips of the rotor which has a diameter of approximately 7 inches.
After exiting the microcooker apparatus, the product flows directly into an eccentric scraped surface heat exchange and is cooled with vigorous agitation to less than 130.degree. F. The cooled product then flows through additional heat exchangers (scraped surface of plate type) to reduce its temperature to less than 55.degree. F.
EXAMPLE 2
Microparticulated Protein Produced from Casein Micelles and Egg White
Microbiologically, aromatically and particulately clean water (16.83 wt. %) produced by a reverse osmosis process is heated in a sanitary tank to about 120.degree. F.
Commercially available apple pectin (0.35 wt. %) dry-blended with sugar (5.0 wt. %) to assure its complete dispersion and is then added to the water in the sanitary tank by means of a high shear solid/liquid Triblender mixer. This mixture is held at about 120.degree.-140.degree. F. with agitation for about 5 minutes to assure hydration and dissolution of the pectin. The mixture is then cooled to less than about 100.degree. F.
Liquid egg white is ultrafiltered using membrane filters having a molecular weight cut-off of about 10,000. The ultrafiltration reduces the total volume of the liquid egg white by about 50% and effectively doubles the protein content and halves the sodium content of the egg white. The treated egg white (55 wt. %) is added to the pectin solution through the suction side of a positive displacement pump with controlled agitation to avoid aeration.
Condensed skim milk (22 65 wt. %) is then added to the mixture through the suction side of a positive displacement pump.
As this mixture is recirculated back to the sanitary tank, a dilute solution of food acid (0.17 wt. %) (acetic, citric, lactic or nydrochloric; alone or in combination) is added through an in-line mixer to lower the pH from about 7 to about 6.20.+-.0.05.
The pH adjusted mix is then rigorously deaerated in a Versator deaerator and bottom-fed into a holding tank which is equipped for non-aerating agitation.
The deaerated mixture is then pumped (600 lb/hr) from the holding tank, by a positive displacement pump through an in-line strainer (300 .mu.m cheesecloth) and a mass flow meter into a plate heat exchanger which heats the mixture to about 165.degree. F., a temperature lower than the target peak temperature which is achieved within the microcooker apparatus described in Example 1. At this lower temperature no coagulate will have developed. Flow is manually-controlled based upon readings from the in-line flow-meter.
The heated mixture is pumped directly from the plate heat exchanger into the microcooker apparatus and the temperature of the mixture is raised to about 185.degree. F. within less than about 10 seconds under high sheer conditions. Rigorous temperature control is maintained over the temperature of the mixture in the microcooker apparatus by a cascade control loop. The control loop senses the temperature of a product exiting the microcooker and holds the temperature constant by regulating the temperature of the mixture leaving the plate heat exchanger.
The speed of the rotor in the microcooker is held constant at about 5400 rpm. At this rpm, the shear rate is about 40,000 reciprocal seconds at the tips of the rotor which has a diameter of approximately 7 inches.
After exiting the microcooker apparatus, the product flows directly into an eccentric scraped surface heat exchanger and is cooled with vigorous agitation to less than 130.degree. F. The cooled product then flows through additional heat exchangers (scraped surface or plate type) to reduce its temperature to less than 55.degree. F.
EXAMPLE 3
Microparticulated Protein Produced from Whey
Commercially available liquid whey is treated by ultrafiltration and evaporation to give a mixture having about 42% by weight solids and about 50%-55% by weight protein, on a dry basis. The resulting whey protein concentrate is deaerated in a Versator deaerator and bottom fed into a sanitary tank equipped for a non-aerating agitation.
The deaerated mixture is then pumped (600 lbs/hr), by a positive displacement pump through an in-line strainer (300 .mu.m cheesecloth), a mass flow meter and plate heat exchanger which raises the temperature of the mixture to about 170.degree. F., into a heated holding device.
The heated holding device includes two concentric scraped surface heat exchangers connected in series. Each heat exchanger provides a hold time of about 3.6 minutes at a flow rate of about 300 lbs/hr. Both of these heat exchangers are heated to maintain the hold temperature set by the plate heat exchanger.
The mixture is then pumped from the holding device to an eccentric scraped surface heat exchanger. This scraped surface heat exchanger cools the mixture to a temperature of about 165.degree. F., a temperature lower than the target peak temperature inside a heat and high shear generating apparatus (microcooker). The mixture then flows directly into the microcooker apparatus as described in Example 1 and the temperature of the mixture is raised to 200.degree. F. within 10 seconds under high shear conditions. Rigorous temperature control at 200.degree. F. is maintained in the microcooker by a cascade control loop. The control loop senses the temperature of a product exiting the microcooker and holds the temperature constant by regulation the temperature of the mixture leaving the eccentric scraped surface heat exchanger.
The speed of the rotor in the microcooker is held constant at about 5200 rpm. At this rpm, the shear rate is about 40,000 reciprocal seconds at the tips of the rotor which has a diameter of approximately 7 inches.
After exiting the microcooker apparatus, the product flows directly into an eccentric scraped surface heat exchanger and is cooled with vigorous agitation to less than 130.degree. F. The cooled product then flows through an additional heat exchanger (scraped surface or plate type) to reduce its temperature to less than 55.degree. F.
EXAMPLE 4
Preparation of a Reduced Fat Sour Cream
A reduced fat sour cream was produced from the ingredients listed in Table 1.
TABLE 1______________________________________Reduced Fat Sour CreamIngredients Wt. % of Composition______________________________________Ultrafiltered Skim Milk (3.times.) 51.4Cream (14% Butterfat) 6.6Nonfat Dry Milk 5.4Microparticulated Protein 10.0(Example 3)Gelatin 0.2Sodium Citrate 0.1Starter System Culture 0.01(FARGO 300 starter culture, Microlife)Rennet 0.0015Flavor 0.15Antimicrobial as neededWater 26.1______________________________________
The ultrafiltered skim milk, nonfat dry milk, cream, gelatin, sodium citrate, antimicrobial (if needed), and water were blended and homogenized in a single stage at 2500 psi. The homogenized mixture was heated to about 185.degree. F. for about 10-30 minutes. The microparticulated protein was added to the hot mixture, the temperature was maintained at 185.degree. F. for about 30 seconds, and then the temperature was lowered to about 70.degree.-78.degree. F. The starter system culture, rennet and flavor were added to the system and the mixture was incubated at about 70.degree.-78.degree. F. for about 12-22 hours to a pH of 4.6-4.8. After incubation, the mixture was cooled to about 40.degree.-65.degree. F., pumped through an in-line screen to smooth the product and packaged.
EXAMPLE 5
Preparation of a Flavored Reduced Fat Sour Cream Dip
A flavored reduced fat sour cream dip is prepared by mixing Lipton dry onion soup mix (1 package) with the reduced fat sour cream (8 oz.) prepared according to the procedures described in Example 4. The mixture is stirred well and stored in a refrigerator until used.
Numerous modifications and variations in practice of the invention are expected to occur to those skilled in the art upon consideration of the foregoing descriptions of preferred embodiments thereof. Consequently, only such limitations should be placed upon the scope of the invention as appear in the appended claims.
Claims
  • 1. A reduced fat sour cream, wherein the improvement comprises replacing all or part of the normal fat and/or oil content of the sour cream with a proteinaceous, water-dispersible, macrocolloid comprising substantially non-aggregated particles of denatured protein having in a dry state a mean diameter particle size distribution ranging from about 0.1 microns to about 2.0 microns, with less than about 2 percent of the total number of particles exceeding 3.0 microns in diameter, and wherein the majority of the said particles are generally spheroidal as viewed at about 800 power magnification under a standard light microscope, the particles in a hydrated state form said macrocolloid having substantially smooth, emulsion-like organoleptic character.
CROSS REFERENCE TO RELATED APPLICATIONS

This application is a continuation-in-part of our copending U.S. patent application Ser. No. 07/367,261 filed June 16, 1989, which issued as U.S. Letters Pat. No. 4,961,953 on Oct. 9, 1990, which is a continuation of our U.S. patent application Ser. No. 07/127,955, filed Dec. 2, 1987, now abandoned, which, in turn, was a continuation-in-part of our U.S. patent application Ser. No. 06/606,959 filed May 4, 1984, which issued as U.S. Letters Pat. No. 4,734,287 on Mar. 29, 1988.

US Referenced Citations (119)
Number Name Date Kind
2377624 Gordon Jun 1945
2566477 Abrahamczik et al. Sep 1951
2602746 Meade Jul 1952
2710808 Peebles et al. Jun 1955
3066133 Pinckney Nov 1962
3300318 Szczesniak et al. Jan 1967
3397997 Japikse Aug 1968
3507663 Starook et al. Apr 1970
3552981 Luksas Jan 1971
3594192 Mullen et al. Jul 1971
3615661 Ellinger et al. Oct 1971
3620757 Ellinger et al. Nov 1971
3632350 Battista Jan 1972
3642490 Hawley et al. Feb 1972
3642492 Arndt Feb 1972
3642493 Arndt Feb 1972
3644326 Pien Feb 1972
3689288 Duren Mar 1972
3708307 Lundstadt Jan 1973
3723407 Miller et al. Mar 1973
3726690 Schuppner Apr 1973
3737326 Basso et al. Jun 1973
3757005 Kautz et al. Sep 1973
3793464 Rusch Feb 1974
3798339 Peng Mar 1974
3800052 Inagami et al. Mar 1974
3829592 Bratland Aug 1974
3842062 Eastman Oct 1974
3843828 Arndt Oct 1974
3852503 Magnino et al. Dec 1974
3853839 Magnino et al. Dec 1974
3865956 Fukushima et al. Feb 1975
3873751 Arndt Mar 1975
3891777 Boyer Jun 1975
3891778 Boyer Jun 1975
3892873 Kolen et al. Jul 1975
3899605 Schaap Aug 1975
3914435 Maubois et al. Oct 1975
3922375 Dalan et al. Nov 1975
3929892 Hynes et al. Dec 1975
3930039 Kuipers Dec 1975
3930056 Feminella et al. Dec 1975
3935323 Feminella et al. Jan 1976
3969534 Pavey et al. Jul 1976
3978243 Pedersen Aug 1976
3982039 Scibelli et al. Sep 1976
4018752 Buhler et al. Apr 1977
4029825 Chang Jun 1977
4031261 Durst Jun 1977
4031267 Berry et al. Jun 1977
4057655 Okada et al. Nov 1977
4058510 Concilio-Nolan et al. Nov 1977
4072670 Goodnight, Jr. et al. Feb 1978
4079154 Yasumatsu Mar 1978
4089987 Chang et al. May 1978
4091116 Edwards et al. May 1978
4103037 Bodor et al. Jul 1978
4103038 Roberts Jul 1978
4104413 Wynn et al. Aug 1978
4107334 Jolly Aug 1978
4113716 Gomi et al. Sep 1978
4125630 Orthoefer Nov 1978
4137339 Kudo et al. Jan 1979
4140808 Jonson Feb 1979
4143174 Shah et al. Mar 1979
4147810 Kellor Apr 1979
4169160 Wingerd et al. Sep 1979
4183970 May et al. Jan 1980
4186218 Gomi et al. Jan 1980
4188411 Kuipers et al. Feb 1980
4192901 Yasumatsu et al. Mar 1980
4194018 Hodel et al. Mar 1980
4194019 Yasumatsu et al. Mar 1980
4205094 Baird et al. May 1980
4209503 Shah et al. May 1980
4212893 Takahata Jul 1980
4217370 Rawlings et al. Sep 1980
4218490 Phillips et al. Sep 1980
4230738 Shemer et al. Oct 1980
4234620 Howard et al. Nov 1980
4244983 Baker Jan 1981
4247566 Inagami et al. Jan 1981
4248895 Stroz et al. Feb 1981
4251562 LeGrand et al. Feb 1981
4252835 Maerker et al. Feb 1981
4259361 Procter Mar 1981
4260636 Yasumatsu et al. Apr 1981
4265924 Buhler et al. May 1981
4267100 Chang et al. May 1981
4271201 Stenne Jun 1981
4275084 Ohyabu et al. Jun 1981
4278597 Cho et al. Jul 1981
4279939 Cho Jul 1981
4291067 Buhler et al. Sep 1981
4293571 Olofsson et al. Oct 1981
4305964 Moran et al. Dec 1981
4305970 Moran et al. Dec 1981
4307118 Kajs Dec 1981
4308294 Rispoli et al. Dec 1981
4325937 Spence et al. Apr 1982
4325977 Remer Apr 1982
4333958 Egnell Jun 1982
4340612 Askman et al. Jul 1982
4352832 Wood et al. Oct 1982
4360537 Tan et al. Nov 1982
4362761 Chang et al. Dec 1982
4379175 Baker Apr 1983
4438148 O'Rourke et al. Mar 1984
4486345 Callewaert Dec 1984
4497834 Barta Feb 1985
4497836 Marquardt et al. Feb 1985
4500454 Chang Feb 1985
4515825 Moran et al. May 1985
4572837 Poole et al. Feb 1986
4675194 Gaffney Jun 1987
4734287 Singer et al. Mar 1988
4762726 Soucie et al. Aug 1988
4885179 Soucie et al. Dec 1989
4975287 Zibell et al. Dec 1990
Foreign Referenced Citations (7)
Number Date Country
0008242 Feb 1980 EPX
0076549 Apr 1983 EPX
7505092 Sep 1976 FRX
8022390 Jul 1982 FRX
236449A1 Jun 1986 DDX
1363783 Aug 1974 GBX
2063273 Jun 1981 GBX
Non-Patent Literature Citations (2)
Entry
Holsinger et al., Food Technology, pp. 59, 60, 64 and 65 (Feb. 1973).
Whitaker et al., Food Proteins, pp. 173-189 (1977).
Continuations (1)
Number Date Country
Parent 127955 Dec 1987
Continuation in Parts (2)
Number Date Country
Parent 367261 Jun 1989
Parent 606959 May 1984