|
|

Link:
Pharm/Biotech Resources
Title: Method for preparing nicotianamine or
nicotianamine-containing product
United States Patent: 6,949,263
Issued: September 27, 2005
Inventors: Asai; Shouji (Chiba, JP); Obata; Akio (Chiba,
JP); Yamazaki; Emiko (Chiba, JP); Kinoshita; Emiko (Chiba, JP); Kikuchi;
Mamoru (Chiba, JP)
Assignee: Kikkoman Corporation (Chiba, JP)
Appl. No.: 011490
Filed: December 11, 2001
Abstract
Precipitation fractionation of an aqueous extract of soybeans by addition
of an organic solvent such as ethanol or molecular weight fractionation of
the extract by ultrafiltration or size exclusion chromatography is
appropriately combined with activated carbon filtration, cation- or
anion-exchange resin treatment or other adsorbent (e.g., polyamide or
octadecylsilica) treatment to provide a nicotianamine product of desired
purity. The product is added to food and drink to provide health foods.
SUMMARY OF THE INVENTION
The inventors studied seeking a method of efficiently preparing
nicotianamine from soybeans or soybean materials. As a result they have
found that addition of an organic solvent to an aqueous extract of soybeans
results in formation of a precipitate, which contains nicotianamine in a
high concentration and that a fraction collected from an aqueous extract of
soybeans which has a molecular weight of 1,000 or less contains
nicotianamine in a high concentration. They have also found that
nicotianamine can be obtained with an economic advantage by utilizing, as an
aqueous extract, soybean whey which is by-produced in the production of
soybean protein isolate.
Based on these findings, the present invention provides a method of
preparing nicotianamine comprising adding an organic solvent to an aqueous
extract of soybeans and purifying the resulting precipitate and a method of
preparing a nicotianamine-containing product comprising adding an organic
solvent to an aqueous extract of soybeans and collecting the resulting
precipitate as a crude product. The present invention also provides a method
of preparing nicotianamine or a nicotianamine-containing product comprising
subjecting an aqueous extract of soybeans to ultrafiltration or size
exclusion chromatography to collect a fraction having a molecular weight of
1,000 or less. The present invention further provides a method for preparing
a nicotianamine-containing product having a nicotianamine content of 0.3% by
weight or more which comprises subjecting an aqueous extract of soybeans to
ultrafiltration or size exclusion chromatography, collecting a fraction
having a molecular weight of 1,000 or less, adding an organic solvent to the
fraction, and collecting the resulting precipitate. The present invention
furthermore provides a health food containing the nicotianamine-containing
product as a functional ingredient.
According to the methods of the present invention, nicotianamine or a
nicotianamine-containing product having ACE inhibitory activity is prepared
efficiently from an aqueous extract of soybeans, particularly soybean whey.
The resulting nicotianamine or nicotianamine-containing product can be taken
as such as a health food or be added to foods to provide health foods for
treating or preventing symptoms of hypertension.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
Soybeans which can be used in the present invention include whole
soybeans, skinned soybeans, ground soybeans, and defatted soybeans used as a
raw material of soy sauce. The aqueous soybean extract includes an extract
of soybeans with water or hot water, a waste liquid used for soaking
soybeans, a waste liquid used for boiling soybeans in the soybean processing
industry, soybean whey by-produced in the manufacture of soybean protein
isolate, and soybean whey by-produced in the manufacture of tofu (soybean
curd).
The aqueous soybean extract may be used as such, but it is advisable to
previously remove dissolved proteins because the proteins may cause
reduction in purity or ACE inhibitory activity of nicotianamine. The
proteins can be removed in a conventional manner, for example, by adjusting
the pH of the extract to about 4.5 to cause them to precipitate.
A suitable aqueous extract of soybeans is prepared by soaking soybeans in 1
to 20 times their weight of water or hot water for at least 5 minutes,
preferably 1 to 20 hours. The extraction is preferably conducted at pH 7 to
9 for extraction efficiency.
An acid is added to the resulting aqueous extract to adjust the pH value to
about 4.5, and the extract is centrifuged to remove the precipitate. The
supernatant is a preferred material. It is particularly advantageous from
the standpoint of utilization of resources to use soybean whey which is
by-produced in the production of soybean protein isolate and has mostly been
discarded.
If desired, the aqueous soybean extract is concentrated, and an organic
solvent is added thereto. A water-soluble organic solvent, such as methanol,
ethanol, and acetone, is used. Ethanol is particularly preferred. The
organic solvent is preferably added in a concentration of 30% (by weight,
hereinafter the same) or more, particularly 50% or more, while the amount
varies depending on the degree of concentration of the extract.
Upon addition of the organic solvent, a precipitate is formed in the aqueous
extract, which is then collected by an appropriate means, such as
centrifugation. The soybean aqueous extract concentrated to a higher degree
tends to form a precipitate easier at a lower concentration of the organic
solvent. For example, where soybean whey obtained by extraction with 10
times the weight of water is used as such, a suitable organic solvent
concentration is 70 to 90%, while a 3- to 4-fold concentrate of the whey
produces a sufficient precipitate at an organic solvent concentration of 50
to 60%.
The precipitate as collected, which contains nicotianamine in a high
concentration, is dried to powder by vacuum drying, lyophilization, or spray
drying to obtain a nicotianamine crude product, which can further be
purified to provide a nicotianamine purified product.
It might be conceivable to directly dry an aqueous extract of soybeans, such
as whey, to powder, but this involves disadvantages arising from various
substances dissolved in the extract such that the resulting nicotianamine
product has nicotianamine of low purity, and the extract is difficult to dry
to powder or fails to provide satisfactory powder.
The crude nicotianamine product can be purified by, for example, the method
described in JP-A-5-246865, Example 2. The physicochemical properties of the
nicotianamine thus prepared are as described in JP-A-5-246865, paragraph
0014.
Impurities can further be reduced by treating the aqueous soybean extract by
ion-exchange resin treatment, activated carbon filtration or adsorbent
treatment or a combination thereof either before or after the organic
solvent addition.
Being ampholytic, nicotianamine can be treated with either a cation-exchange
resin or an anion-exchange resin. Since nicotianamine has high polarity and
is thereby substantially inert to activated carbon, treatment with activated
carbon removes oligosaccharides or like impurities present in soybean whey.
To remove organic matter of relatively low polarity, such as isoflavons and
saponins, the extract can be treated with octadecylsilica, polyamide,
synthetic adsorbents (e.g., Diaion HP-20, available from Mitsubishi Chemical
Corp.), etc.
Nicotianamine, the molecular weight of which is 303, is able to pass through
an ultrafiltration membrane having a molecular weight cut-off of about 1,000
even when it is in the form of a salt. When subjected to size exclusion
chromatography, it can be collected in a fraction of molecular weight 1,000
or less. Therefore, it is also possible to recover nicotianamine or a
nicotianamine-containing product from an aqueous soybean extract such as
soybean whey by ultrafiltration or size exclusion chromatography to collect
a fraction having a molecular weight of 1,000 or less.
Nicotianamine or a nicotianamine-containing product with higher purity can
be obtained by treating the aqueous soybean extract by ion-exchange resin
treatment, activated carbon filtration or adsorbent treatment or a
combination thereof either before or after ultrafiltration or size exclusion
chromatography as described above.
The nicotianamine-containing product of the present invention can be
desalted by electrodialysis or a like means. The dialyzate, which contains
nicotianamine in a high concentration, is dried to powder by vacuum drying,
lyophilization or spray drying to obtain a crude nicotianamine product,
which can further be purified by the above-mentioned purification techniques
to prepare a purified nicotianamine product. Purification can be effected to
a desired degree according to the intended use of the product.
The above-described method comprising adding an organic solvent and the
method comprising ultrafiltration or size exclusion chromatography can be
combined to provide a nicotianamine-containing product having a
nicotianamine content of 0.3% or more. In this case, also, the
above-described treatment with an ion-exchange resin, activated carbon or an
adsorbent or a combination thereof can be performed either before or after
addition of an organic solvent or either before or after ultrafiltration or
size exclusion chromatography. For example, an aqueous soybean extract,
preferably soybean whey, is treated by activated carbon filtration, and the
filtrate is subjected to ultrafiltration or size exclusion chromatography to
harvest a fraction having a molecular weight of 1,000 or smaller. An organic
solvent is then added to the fraction in a concentration of 30%, and the
precipitate thus formed is collected to give a nicotianamine-containing
product having a nicotianamine content of 0.3% or more.
The present invention also provides a health food containing the
nicotianamine or nicotianamine-containing product (a crude product or a
purified product) obtained by the method of the invention as a functional
ingredient. For example, the crude nicotianamine-containing product is mixed
with common vehicles and punched into tablets or incorporated into a variety
of foods and beverages, such as bakery products (e.g., bread, cake, and
cookies), noodles (e.g., buckwheat noodle, wheat noodle, and Chinese
noodle), cooked foods (e.g., tempura or deep-fried foods), soybean foods
(e.g., tofu and natto (fermented soybeans)), juice, coffee, cocoa, woolong
tea, green tea, and health drinks, to make functional food and drink having
antihypertensive activity of nicotianamine.
The present invention will now be illustrated in greater detail with
reference to Examples. Unless otherwise noted, all the percents and parts
are by weight.
EXAMPLE 1
To 400 g of defatted soybean meal was added 5 l of water, and water was
adjusted to pH 9. After 90-minute soaking at 25° C., the soybean meal was
separated to obtain 4.7 l of the aqueous extract. The extract was adjusted
to pH 4.5 and centrifuged at 7500 G for 30 minutes to obtain 4.5 l of the
supernatant liquid (soybean whey). Ethanol was added to the whey to a
concentration of 80%, followed by centrifugation at 4° C. and at 7500 G for
30 minutes. The collected precipitate was lyophilized to give 12 g of a
crude nicotianamine product as white powder, which was found to have a
nicotianamine content of 0.5%.
EXAMPLE 2
To 4.5 l of soybean whey prepared in the same manner as in Example 1 was
added 150 g of activated carbon (Shirasagi, available from Takeda Chemical
Industries, Ltd.), and the mixture was stirred at room temperature for 3
hours to have impurities adsorbed onto the activated carbon. Into the
mixture was mixed 150 g of a diatomite filter aid (Radiolite 500), and the
mixture was filtered by suction through filter paper No. 2. The filtrate was
treated through a hollow fiber type ultrafiltration membrane module having a
molecular weight cut-off of 1,000 (Prepscale UF Cartridge, PLAC type,
available from Nihon Millipore K.K.). The ultrafiltrate was lyophilized to
give 30 g of a white powder, which was found to have a nicotianamine content
of 0.3%.
EXAMPLE 3
The powder obtained in Example 2 was re-dissolved in 200 ml of distilled
water, and ethanol was added to a concentration of 80%. The ethanol solution
was centrifuged at 4° C. and at 7500 G for 30 minutes. The collected solid
was lyophilized to obtain 5.4 g of a crude nicotianamine product as a white
powder, which contained 1.0% of nicotianamine.
EXAMPLE 4
The ultrafiltrate obtained in Example 2 was passed through a 1-l column of
an anion-exchange resin (Diaion PA318, OH- form, available from
Mitsubishi Chemical Corp.). The column was washed with 2 l of distilled
water and eluted with 2 l of 0.5N hydrochloric acid. The eluate was further
passed through a 1-l column of a cation-exchange resin (Dowex 50W×2, H+
form, available from the Dow Chemical Co.), and the column was washed with 2
l of distilled water and eluted with 0.5% aqueous ammonia. The fraction of
from 2 l up to 3 l was collected and concentrated to 10 ml on a rotary
evaporator. The concentrate was lyophilized to give 100 mg of a white
powder, which had a nicotianamine content of 40%.
Claim 1 of 3 Claims
1. A method of preparing a nicotianamine-containing product having a
nicotianamine content of 0.3% by weight or more which comprises subjecting
an aqueous extract of soybeans to ultrafiltration or size exclusion
chromatography to collect a fraction having a molecular weight of 1,000 or
less, adding an organic solvent to the fraction, and collecting the
resulting precipitate.
____________________________________________
If you want to learn more
about this patent, please go directly to the U.S.
Patent and Trademark Office Web site to access the full
patent.
|