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Program Book - Master Brewers Association of the Americas

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Poster Session: Premature Yeast Flocculation<br />

Moderator: Fateh Sodha, Molson-Coors Brewing Company, Golden,<br />

CO<br />

Fateh Sodha is <strong>the</strong> process manager in <strong>the</strong> Brewing Department<br />

at Coors Brewing Company. In his 10 years at Coors Brewing<br />

Company, he has worked in <strong>the</strong> chemistry and microbiology labs,<br />

quality control, and as <strong>the</strong> fermentation and yeast manager. Fateh<br />

has a B.S. degree in anthropology, with an emphasis in biology,<br />

and a M.S. degree in medical anthropology from <strong>the</strong> University <strong>of</strong><br />

Colorado, and he recently sat for his diploma in brewing exam. He is<br />

a member <strong>of</strong> IBD and ASBC.<br />

P-183<br />

Investigation <strong>of</strong> <strong>the</strong> causes <strong>of</strong> PYF malt using a modified<br />

analytical method for <strong>the</strong> PYF potential<br />

KATSUYA SASAKI (1), Hiroshi Yamashita (1), Katsunori Kono (1),<br />

Yasushi Kitagawa (1)<br />

(1) Asahi Breweries Ltd., Moriya-shi, Japan<br />

Premature yeast flocculation (PYF) is a serious problem in <strong>the</strong><br />

brewing industry because it causes low attenuation and results in<br />

an undesirable flavor in beer. The PYF phenomenon is induced<br />

by certain malts, which we call “PYF malts.” To overcome <strong>the</strong><br />

PYF malt issue, it is important to study in detail <strong>the</strong> relationship<br />

between <strong>the</strong> actual malting conditions and <strong>the</strong> PYF potential <strong>of</strong><br />

<strong>the</strong> malt using reliable analytical methods. Our approach to <strong>the</strong><br />

PYF issue is presented here in three stages. 1) Development <strong>of</strong> a<br />

reliable analytical method for PYF potential: <strong>the</strong>re have been several<br />

analytical methods for estimating PYF potential. However, <strong>the</strong>y<br />

frequently have problems with repeatability because <strong>of</strong> unstable<br />

fermentation. We found that putting in a boiling stone or similar<br />

object to release <strong>the</strong> CO 2 dissolved in <strong>the</strong> fermentation wort made<br />

small-scale fermentations stable. High repeatability was obtained<br />

on a 50-ml scale fermentation, and this allowed us to carry out a<br />

quantitative analysis. In addition, we succeeded in developing a 3-ml<br />

scale fermentation test in a spectrophotometer cuvette. This has<br />

advantages for research in which many samples need to be analyzed<br />

at <strong>the</strong> same time. 2) Investigation <strong>of</strong> <strong>the</strong> causes <strong>of</strong> PYF malt: our<br />

studies on <strong>the</strong> localization <strong>of</strong> PYF factors and micromalting tests<br />

using infected barley suggest that one <strong>of</strong> <strong>the</strong> causes might be<br />

infections from microorganisms on <strong>the</strong> barley. We screened more<br />

than thirty kinds <strong>of</strong> fungi from <strong>the</strong> PYF malt and investigated<br />

which <strong>of</strong> <strong>the</strong>m caused PYF in <strong>the</strong> malt. Malts made from barleys<br />

infected with five strains <strong>of</strong> fungi were shown to be PYF positive,<br />

and <strong>the</strong> fungi were identified. In parallel with this, <strong>the</strong> influence<br />

<strong>of</strong> steeping conditions on PYF were investigated in a micromalting<br />

facility. Steeping with no aeration increased <strong>the</strong> PYF potential<br />

compared with aeration. 3) Monitoring <strong>of</strong> <strong>the</strong> PYF potential <strong>of</strong><br />

all <strong>the</strong> malt samples shipped in 2006–2007: <strong>the</strong> PYF potential <strong>of</strong><br />

every malt sample shipped was routinely analyzed using a 50-ml<br />

scale fermentation test. We will report <strong>the</strong> frequency <strong>of</strong> PYF malt<br />

found among <strong>the</strong>m. We observed that PYF malts were produced<br />

continuously from certain malting plants, even when no PYF malt<br />

was found in o<strong>the</strong>r malting plants using barley from <strong>the</strong> same area.<br />

This suggests that in addition to <strong>the</strong> quality <strong>of</strong> <strong>the</strong> barley, <strong>the</strong> malting<br />

process is also an important factor.<br />

Katsuya Sasaki is a research worker at <strong>the</strong> Research Laboratories<br />

<strong>of</strong> Brewing Technology, Asahi Breweries, Ltd. in Ibaraki, Japan.<br />

He received his M.S. degree in engineering from Tokyo Institute<br />

<strong>of</strong> Technology in 1998 and joined Asahi Breweries, Ltd. He has<br />

researched malt quality and malting technology.<br />

156<br />

P-184<br />

A new method to measure yeast flocculation activity in<br />

malt using lectin (concanavalin A) coated quartz crystal<br />

microbalance (QCM)<br />

HIDEKI TSUDA (1), Masahiro Gomi (1), Takeo Imai (1), Atsushi<br />

Murakami (1), Yutaka Ogawa (1)<br />

(1) Kirin Brewery Company Limited, Research Laboratories for<br />

Brewing, Yokohama, Japan<br />

Premature yeast flocculation (PYF) is <strong>the</strong> phenomenon whereby<br />

yeast flocculates prior to depletion <strong>of</strong> nutrients in <strong>the</strong> wort.<br />

Because this interferes, PYF causes low attenuation and results<br />

in an undesirable flavor in beer. PYF is caused by a substance<br />

called premature yeast flocculation-inducing factor (PYF-factor)<br />

in malt. It has been reported that PYF-factor is a high molecular<br />

weight polysaccharide. Never<strong>the</strong>less it is very important for<br />

brewers to measure yeast flocculation activity or to detect PYF<br />

activity in malt, only a fermentation test has been applied as <strong>the</strong><br />

conventional method for a long time. A fermentation test is a test<br />

wherein <strong>the</strong> actual fermentation is performed with wort and yeast<br />

in a small scale taking into account yeast growth and gravity <strong>of</strong> <strong>the</strong><br />

wort. A fermentation test is a kind <strong>of</strong> bio-assay, results from <strong>the</strong><br />

fermentation test fluctuate and are influenced by <strong>the</strong> yeast condition<br />

and nutrients in wort. In order to dissolve this problem, many<br />

devices or protocols have been developed. However, a new method,<br />

which does not need yeast and fermentation, has never been<br />

reported. Therefore, we have developed a new method to measure<br />

yeast flocculation activity in malt without using a fermentation test.<br />

This method is very unique because yeast flocculation activity is<br />

measured using Concanavalin A coated quartz crystal microbalance.<br />

Concanavalin A is a lectin purified from Jack bean (Canavalia<br />

ensiformis). It has been reported that Concanavalin A has an affinity<br />

to PYF-factor. Quartz crystal microbalance (QCM) uses <strong>the</strong> nature<br />

<strong>of</strong> <strong>the</strong> quartz crystal which has a characteristic frequency that<br />

decreases regularly when something binds on <strong>the</strong> quartz crystal<br />

surface. We made a QCM sensor coated with Concanavalin A. Our<br />

method is composed <strong>of</strong> four steps: 1) <strong>the</strong> malt extract is prepared<br />

from <strong>the</strong> congress wort by <strong>the</strong> conventional HPLC technique,<br />

2) a Concanavalin A coated QCM sensor and <strong>the</strong> malt extraction<br />

are mixed in <strong>the</strong> acid buffer, 3) <strong>the</strong> frequency <strong>of</strong> <strong>the</strong> QCM sensor<br />

changes (decreases) responding to <strong>the</strong> amount <strong>of</strong> <strong>the</strong> PYF-factor<br />

included in <strong>the</strong> malt extraction, and 4) <strong>the</strong> frequency change<br />

during 60 seconds is defined as <strong>the</strong> yeast flocculation activity in<br />

<strong>the</strong> original malt. As a result <strong>of</strong> <strong>the</strong> test with nine malt samples, <strong>the</strong><br />

yeast flocculation activity measured by our method correlated well<br />

with that measured using a fermentation test. Using our method, we<br />

were able to measure <strong>the</strong> yeast flocculation activity or to detect PYF<br />

activity in malt without yeast and fermentation.<br />

Hideki Tsuda received a M.S. degree in agricultural chemistry from<br />

Tohoku University in Sendai, Japan. He entered Kirin Brewery<br />

Company, Ltd. in April 1993. After working in <strong>the</strong> malting and<br />

brewing area, he was assigned to <strong>the</strong> Research Laboratory for<br />

Brewing in 2004.

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