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Article
Formation of Guaiacol by Spoilage Bacteria from Vanillic Acid, a Product of Rice Koji Cultivation, in Japanese Sake Brewing. Toshihiko Ito, Mahito Konno, Yoichiro Shimura, Seiei Watanabe, Hitoshi Takahashi, and Katsumi Hashizume J. Agric. Food Chem., Just Accepted Manuscript • DOI: 10.1021/acs.jafc.6b01031 • Publication Date (Web): 15 May 2016 Downloaded from http://pubs.acs.org on May 21, 2016
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Journal of Agricultural and Food Chemistry
RESEARCH ARTICLE
TITLE: Formation of Guaiacol by Spoilage Bacteria from Vanillic Acid, a Product of Rice Koji Cultivation, in Japanese Sake Brewing.
AUTHORS: Toshihiko Ito, # Mahito Konno, # Yoichiro Shimura, # Seiei Watanabe, § Hitoshi Takahashi, § and Katsumi Hashizume * , #
AFFILIATIONS:
#
Department of Biological Resource Sciences, Akita
Prefectural University, Nakano Shimoshinjyo, Akita 010-0195, Japan §
Akita Research Institute for Food & Brewing, 4-26 Sanuki, Araya-machi,
Akita 010-1623, Japan
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ABSTRACT
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The formation of guaiacol, a potent phenolic off-odor compound in the Japanese
3
sake brewing process, was investigated.
4
and one contained guaiacol and 4-vinylguaiacol (4-VG) at extraordinary high
5
levels: 374 and 2433 µg/kg dry mass koji, respectively. All samples contained
6
ferulic and vanillic acids at concentrations of mg/kg dry mass koji. Guaiacol
7
forming microorganisms were isolated from four rice koji samples.
8
identified as Bacillus subtilis, B. amyloliquefaciens/subtilis, and Staphylococcus
9
gallinarum using 16S rRNA gene sequence.
Eight rice koji samples were analyzed,
They were
These spoilage bacteria convert
10
vanillic acid to guaiacol and ferulic acid to 4-VG.
However, they convert very
11
little ferulic acid or 4-VG to guaiacol. Nine strains of koji fungi tested produced
12
vanillic acid at the mg/kg dry mass koji level after cultivation. These results
13
indicated that spoilage bacteria form guaiacol from vanillic acid, which is a
14
product of koji cultivation in the sake brewing process.
15 16 17
KEYWORDS: guaiacol, vanillic acid, spoilage bacteria, koji, sake brewing
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INTRODUCTION
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Phenolic acids, represented by ferulic acid, contained in the plant cell wall are
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bio-catalytically degraded by microorganisms which often produce volatile
22
phenols, for example; 4-vinyl guaiacol (4-VG) or guaiacol.1-2 In the
23
degradation process, bioconversion of vanillic acid to guaiacol has been found
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in Rhodotorula yeast, Bacillus, Pseudomonas and Streptomyces bacteria.3-6
25
Guaiacol has been recognized as a potent phenolic off-odor compound of
26
Alicyclobacillus spoilage in apple or other fruit juices, and its formation has
27
been eagerly studied.7-9
28
preparations,10-11 and has been identified in wines that have been barrel-aged
29
or aged with toasted oak chips and staves 12-13 or wines made using grapes that
30
have been affected by bushfire smoke.14
31
specific marker for torrefied malts and its levels in beer increase with age.15
32
addition to guaiacol, 4-VG, 4-vinylphenol (4-VP), 4-ethylguaiacol (4-EG), and
33
4-ethylphenol (4-EP) are known as influencing phenolic off-odor constituents in
34
wines.16-17
35
Pof+ Saccharomyces cerevisiae, lactic acid and other bacteria in the wine
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making process, while 4-EG and 4-EP are formed by Bretanomyces/Dekkera
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sp. spoilage yeast.16
38
ferulic acid by Pof+ beer yeast and it is also formed during thermal processing in
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beer production.18
40
wheat Qu, a moulded cereal used as a saccharifying enzyme source, rather
41
than from yeast.19
42
It is a representative constituent of smoke flavoring
In beer brewing, guaiacol is a In
4-VG and 4-VP are formed by various microorganisms, including
A previous report suggested that 4-VG is formed from
In Chinese rice wine production, 4-VG originates from
Japanese sake, a traditional alcoholic beverage, is made from polished
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rice, rice koji, and water.
The polished rice is steamed after soaking and used
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for moromi mash preparation or rice koji cultivation (Figure 1). Solid state
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fermentation by koji mold, Aspergillus oryze, produces a variety of enzymes
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and metabolites required for alcoholic fermentation of the moromi mash.
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Ferulic and p-coumaric acids are released from ingredient rice grains during the
48
fermentation process and they may be converted to 4-VG and 4-VP by
49
Staphylococcus and/or Bacillus species.20
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reduced to 4-EG and 4-EP by Pichia spoilage yeast.20
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that guaiacol contributes to the 4-VG-like phenolic off-odor in sake, 21 however,
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its formation in the sake brewing process has never been studied.
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maximum temperature reached in the sake brewing process is ca. 100 ℃ in
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the steaming rice which is far lower than the temperature in the torrefied malts
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making process (final roasting temperature reaches 225 ℃) 15 where guaiacol
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is produced by thermal reaction.
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sake brewing factories, suggesting spoilage microorganisms were involved in
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its production.
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microbiological factors affecting on guaiacol formation in the Japanese sake
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brewing process, focusing on rice koji cultivation process in which the so-called
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open fermentation style is employed, in which contamination with spoilage
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microorganisms is possible. Volatile phenols and phenolic acids in rice koji
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were quantitated and guaiacol forming microorganisms in the rice koji were
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isolated and identified.
4-VG and 4-VP are sometimes Recently, we reported
The
Guaiacol was originally detected in particular
The aim of this study was to elucidate chemical and
65 66
MATERIALS AND METHODS
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Chemicals.
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2-Methoxyphenol (guaiacol) (98%) was purchased from Tokyo Chemical
69
Industry Co. (Tokyo, Japan).
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4-ethyl-2-methoxyphenol (4-ethylguaiacol) (95%), 3-methylphenol (m-cresol)
2-Methoxy -4-vinylphenol (4-vinylguaiacol),
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(98%), 4-methyphenol (p-cresol), 4-ethylphenol (95%), 2-6-dimethoxyphenol
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(98%) , 4-hydroxybenzoic acid (95%), 4-hydroxyphenylacetic acid (98%),
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4-hydroy-3-methoxybenzoic acid (vanillic acid) (95%), 4-hydroxycinnamic acid
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(p-coumaric acid) (98%), 4-hydroxy-3-methoxycinnamic acid (ferulic acid) (98%),
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3,5-dimethoxy-4-hydroxycinnamic acid (sinapic acid) (97%),
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4-hydroxy-3,5-dimethoxybenzoic acid (syringic acid), 4-n-butylphenol, ethanol
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(95%), ethyl acetate (infinity pure grade) and methanol were obtained from Wako
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Pure Chemical Industry Co. (Osaka, Japan).
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pyridine were obtained from Sigma-Aldrich Japan Co. (Tokyo, Japan).
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Acetonitrile (LC/MS grade) and BSTF+10 % TMCS were obtained from Thermo
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Fisher Scientific Co. (Kanagawa, Japan)
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Materials. Eight rice koji samples from 4 sake brewing factories (2 samples
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from each) in the Akita prefecture were used.
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until use.
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guaiacol sake, as reported in our previous study.21 Strains of Aspergillus oryzae
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were kindly gifted by the National Research Institute of Brewing
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(Higashihiroshima, Japan)
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Analysis of Volatile Phenols in Rice Koji.
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mL of a 23.8 % (v/v) ethanol aqueous solution and stirred at 120 rpm for 3 h at
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30 °C.
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was diluted with an equal volume of distilled water. Volatile phenols in the
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diluted sample were analyzed by GC-MS after its preparation as an ethyl acetate
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extract (Figure S1), according to our previously reported method for sake
94
samples.21
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limits for guaiacol and 4-VG were 0.3 and 0.7 µg/L in the extract, and 1.6 and 3.7
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µg/kg dry mass koji, respectively.
4-Vinylphenol solution and
Samples were stored at -20 °C
Factories C and D (Table 1) were selected because of their high
Rice koji (4 g) were mixed with 20
The solution was then filtered using filter paper. The filtrate (10 mL)
4-n-Butylphenol was used as an internal standard. The detection
The recovery rate for guaiacol spiked at 50
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µg/L was 104.5±10.1 % and 91.9 ±1.7 % for 4-VG spiked at 200µg/L.
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moisture content of rice koji samples was measured using the loss of sample
99
weight after drying at 135 °C for 3 h.
The
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Analysis of Phenolic Acid in Rice Koji. Phenolic acids in the rice koji were
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identified by GC-MS after solvent extraction, condensation, HPLC fractionation,
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and trimethylsilylation.
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ethanol aqueous solution and stirred at 120 rpm for 90 min at 30 °C. The
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extract was obtained through paper filtration. After ethanol removal by rotary
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evaporation (60 °C, 120 hPa), the pH of the aqueous solution was adjusted to
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1.4 with 1 M H2SO4 and then applied to a pre-conditioned Bond Elute C18 LRC
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500MG (Agilent Technologies, Santa Clara, CA, USA).
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washed with water and trapped constituents were eluted with 2 mL of methanol.
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The solution was concentrated to ca. 100 µL by rotary evaporation (60 °C, 40
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hPa) and then fractionated by HPLC using a Capcell Pak C18 Type MG column
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(4.5 mm x 250 mm)(Shiseido, Tokyo, Japan).
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solvent B was 0.1 % phosphoric acid / water.
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A: B=5: 95 to A: B=25: 75 over 30 min at a flow rate of 1.0 mL/min. The
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absorbance at 280 nm was monitored. Each peak fraction was collected and
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dried under vacuum and methylsilylated using a mixture of 100 µL of
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BSTF+10 % TMCS and pyridine at 70 °C for 15 min.
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analyzed using 7890A GC/5975C inert XL MSD (Agilent Technologies)
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apparatus and a fused silica column (30 m x 0.25 mm i.d., coated with a 0.25 µm
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film of DB-5MS; Agilent Technologies) using splitless injection mode.
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column temperature was held at 80 °C for 8 min and then raised from 80 °C to
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220 °C at a rate of 6 °C/min and held for 10 min at 220 °C.
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temperature was 220 °C, and the flow rate of the helium carrier gas was 1.5
Rice koji (4 g) was mixed with 20 mL of a 38 % (v/v)
The column was
Solvent A was acetonitrile, and
A linear gradient was used from
The sample (2 µL) was
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The injector
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mL/min. The mass spectrometer was used with an ionization voltage of 70 eV
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(EI) and an ion source temperature of 230 °C.
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comparison with the retention time and mass spectrum of the trimethylsilylated
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authentic phenolic acid and the NIST library.
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conducted by HPLC without trimethylsilylation, applying 20 µL of the same
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extract solution used for the volatile phenol analysis (Figure S2). HPLC
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conditions were the same as the fractionation experiment. Quantitation was
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performed using an external calibration method. Calibration curves were
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constructed using 23.8% ethanol aqueous solutions of standard phenolic acids.
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They showed good linearity (R2=0.9994 - 1.000) and detection limits for vanillic
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and ferulic acids were 0.01 and 0.02 mg/L, and 0.07 and 0.08 mg/kg of koji
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sample, respectively.
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acids at 0.667 mg/L in the extracted solution were 97.1 ± 7.0 % and 100.5 ±
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9.3 %, respectively.
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Isolation of Microorganisms able to Convert Vanillic Acid to Guaiacol.
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YSG media (pH 3.722 and pH 6.1 without pH adjustment) were used in the
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isolation. Ten grains of rice koji were suspended in a Tween 20 aqueous
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solution (0.05 % (v/v)). After vigorous mixing, the liquid phase was diluted and
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inoculated onto an agar (3%) plate. After incubation at 30 °C for 24-48 h,
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formed colonies were picked and inoculated into the liquid media (5 mL,
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containing 10 mg/L vanillic acid) and cultivated at 30 °C for 24 h, with shaking at
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120 rpm.
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and HPLC. HPLC conditions were the same as for analysis of phenolic acid,
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with one exception; a gradient condition was changed to A: B=40: 60 to A: B=60:
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40 over 30 min. Guaiacol forming ability of the isolated microorganism was
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confirmed repeatedly by plate and liquid cultivation tests.
Components were identified by
Quantitation of phenolic acids was
The percentage recovery of spiked vanillic and ferulic
Other phenolic acids tested also showed similar results.
Phenolic compounds in the liquid media were analyzed by smelling
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Identification of Isolated Microorganism. Isolated microorganisms were
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identified with 16S rRNA gene sequence using NCBI-BLAST
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(https://blast.ncbi.nlm.nih.gov/); The gene was amplified by PCR using the 27F
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and 1492R primer pair, the amplified fragment was sequenced using 27F, 519F,
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1114F, 518R, 806R, and 1492R primers,23-27 and then merged sequence was
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applied to the BLAST program.
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Bioconversion Ability of Phenolic Compounds from the Isolated
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Microorganism. An aliquot (0.2 mL) of pre-cultivated microorganism in YSG
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liquid medium (pH 6.1) was inoculated into 5 mL of liquid media (pH 6.1)
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containing phenolic compounds at 10 mg/L.
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shaking at 120 rpm.
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After cultivation, the gas in the head space of the glass tube was inhaled to
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check for guaiacol odor. The sample was centrifuged at 14,000 × g for 10 min,
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and a 20 µL aliquot was applied to HPLC. Quantitation was performed using an
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external calibration method.
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23.8% ethanol aqueous solution of standard phenolic compounds except for
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2,6-dimethoxy-4-vinylphenol.
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0.06 and 0.03 mg/L, respectively.
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(canolol) was confirmed by its GC-MS spectrum,27 and the concentration was
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estimated by the molecular absorbance coefficient value.28 When ferulic or
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vanillic acid were tested as substrates, guaiacol was analyzed using GC-MS
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according a previously reported method.21
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Effects of Ethanol Concentration and pH on Growth and Guaiacol
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Formation in the Isolated Microorganism.
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the liquid medium containing vanillic acid at 10 mg/L was adjusted by adding a
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95 % aqueous ethanol solution and the pH was adjusted by the addition of lactic
It was cultured at 30 °C for 24 h,
Formed phenolic compounds were determined by HPLC.
Calibration curves were constructed using a
The detection limits for guaiacol and 4-VG were Formation of 2,6-dimethoxy-4-vinylphenol
The concentration of ethanol in
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acid. To test pH, ethanol was not added to the media.
Cultivation was
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conducted under the same conditions as the test for bioconversion ability. Cell
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growth was monitored by absorbance at 660 nm and guaiacol formation was
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analyzed by HPLC, as mentioned above.
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Analysis of Phenolic Acid in the Rice Koji Cultivation Process.
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of 60 % polished rice grain was soaked in water for 1 h, the water absorbance of
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the soaked rice grains was adjusted to 30 %. The rice was then steamed for 50
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min and cooled to room temperature, before it was put into a 300 mL Erlenmeyer
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flask and autoclaved at 110 °C for 15 min.
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oryzae (RIB128) spores was inoculated and mixed.
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for 22 h, the mix was transferred to two sterilized plastic plates (90 mm) and
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cultivated at 35 °C for 19 h, and then 37 °C for 7 h covered with filter paper.
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oryzae cultivation was initiated by the addition of one rice grain of the koji seed
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which contained adequate spores for the strain comparison test.
Phenolic acid
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was analyzed using the same conditions for the rice koji sample.
Production of
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phenolic acid by A. oryzae RIB128 was also examined using a Czapek-Dox agar
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plate (0.3 % NaNO3, 0.1 % K2HPO4, 0.05 % KCl, 0.05 % MgSO47H2O,
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0.001 % FeSO47H2O, 0.01 % glucose, 0.5 % starch, 3.0 % agar, 20 mg/L
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phenolic acid) by cultivating at 30 °C for 3 days.
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was sampled and mixed with an equal weight of 70 % (v/v) aqueous ethanol
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solution. After extraction at 30 °C for 90 min at 120 rpm, the supernatant
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solution was analyzed by HPLC.
After 40 g
After cooling, 1 mg of Aspergillus After cultivation at 30 °C
A.
Agar medium and fungus body
197 198
RESULTS AND DISCUSSION
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Quantitation of Phenolic Compound in Rice Koji. The concentrations of
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volatile phenols in rice koji samples are shown in Table 1.
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Guaiacol was only
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found in one sample (no. 7, factory D). It contained guaiacol and 4-VG at
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extraordinary high levels, 374 and 2433 µg/kg dry mass koji, respectively.
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There was little difference in the concentration of other volatile phenols among
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the other samples. Sample no. 7 showed the highest water content. The
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water-rich koji culture conditions may be profitable for bacterial growth. In the
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common sake brewing process, rice koji is used at 20 % of the total rice material,
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and ca. 2.15 L of jyunmai-type sake was brewed from 1 kg of rice (Figure 1) the
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volatile phenols in the koji sample are diluted about ten times. Sample no. 7
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may produce guaiacol and 4-VG in the brewed out sake at the sensory
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acceptable level (guaiacol, 14.6 µg/L: 4-VG, 141 µg/L),21 if volatile phenols in the
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rice koji are transferred to sake with no decrease in concentration.
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value in sample no. 7 may be due to vigorous bacterial activity which often
213
produces organic acids. More than 45 years ago, Nakamura et al. reported that
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rice koji used in sake brewing contained vanillic acid and several other phenolic
215
acids,29 howerver, no further studies on vanillic acid in rice koji for sake brewing
216
have been reported.
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after HPLC fractionation and trimethylsilylation: p-hydroxybenzoic,
218
p-hydroxyphenylacetic, vanillic, and syringic acids were detected. The level of
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syringic acid was far lower than the other phenolic acids. After identification,
220
phenolic acids were quantitated by HPLC without trimethylsilylation.
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p-Hydroxybenzoic, p-hydroxyphenylacetic and vanillic acids were present at
222
more than 1.0 mg/kg dry mass in all samples (Table2). The amount of ferulic
223
acid was higher than 2.7 mg/kg dry mass in all samples which was comparable
224
to that of previous report.30
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Isolation and Identification of Microorganisms Forming Guaiacol from
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Vanillic Acid in Rice Koji. An isolation trial using YSG medium (pH 3.7)22
The low pH
We analyzed phenolic acids in the sample no.1 by GC-MS
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suitable for detection of Alicyclobacillus sp. bacteria did not find any
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microorganisms in the rice koji samples. A subsequent study using YSG
229
medium without pH adjustment (pH 6.1) produced many colonies after
230
incubation at 30 °C for 24-48 h. Each colony was tested for guaiacol forming
231
ability using liquid medium containing vanillic acid at 10 mg/L.
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microorganisms were isolated from sample no. 3, 6, 7, and 8 (Table 3).
233
Samples no. 6, 7 and 8 were from high guaiacol sake producing factories,
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whereas sample no. 3 was not. Three of the microorganisms were identified as
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Bacillus sp. and the other 2 microorganisms were Staphylococcus sp.
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Kaneoke20 reported that S. gallinarum is a spoilage bacteria in the sake brewing
237
process that produces 4-VG from ferulic acid, however the Bacillus sp. bacteria
238
found in this study were different to those previously reported.20 It has been
239
reported that B. subtilis is able to form guaiacol from vanillic acid,6, 31 and it also
240
may decarboxylate p-coumaric acid and ferulic acid to form 4-VP and 4-VG.32
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Thus, the isolated spoilage bacteria have an ability to convert various phenolic
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compounds.
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Bioconversion Ability of Isolated Bacteria. Three of the bacteria isolated
244
were examined for their bioconversion ability of various phenolic compounds
245
using YSG liquid media (pH 6.1) containing phenolic compounds at 10 mg/L.
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Ferulic, vanillic and p-coumaric acids were rapidly decarboxylated by the three
247
bacteria but only B. subtilis decarboxylated sinapic and syringic acids (Table 4).
248
In contrast, the three bacteria showed little ability for the bioconversion of 4-VG
249
to guaiacol. In both tests of ferulic acid and 4-VG addition, the characteristic
250
odor of guaiacol was detectable by smelling, however, it was not detected by
251
HPLC. Hence we analyzed it by GC-MS.
252
low. It was suggested that the bacterial conversion abilities were enough to
The
The determined level was extremely
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produce the level of guaiacol measured in rice koji sample no.7 from vanillic acid.
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Since the observed guaiacol forming ability of the isolated bacteria was
255
comparable, high guaiacol level in samples no.7 might be due to the high levels
256
of both bacteria in the koji culture.
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Effects of Ethanol Concentration and pH on the Growth and Guaiacol
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Formation of Isolated Bacteria.
259
pH are important factors in protecting moromi mash from bacterial spoilage: the
260
effects of these two factors on growth and guaiacol formation in isolated bacteria
261
were examined (Figure 2-A, 2-B).
262
gallinarum were suppressed at 5 % (v/v) of ethanol, while Bacillus sp. were
263
suppressed at 10 % (v/v) ethanol. In contrast, low pH, less than 4, suppressed
264
growth and guaiacol formation in all bacteria. In the common sake brewing
265
process, the pH of the fermentation starter is adjusted to below 4.0 at the starting
266
point of cultivation by lactic acid to suppress spoilage bacteria. In the early
267
stage of the kimoto starter making process, a traditional fermentation starter
268
method prepared by mixing only steamed rice, rice koji, and water, the pH is
269
greater than 5 which may permit bacterial growth, and lead to higher guaiacol
270
production. Our results showed that Bacillus sp. produced higher levels of
271
guaiacol per absorbance (growth) than S. gallinarum, indicating that Bacillus sp.
272
might cause more serious spoilage effects when they grow.
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Analysis of Phenolic Acid in the Rice Koji Cultivation Process.
274
isolated bacteria had low conversion rates for ferulic acid or 4-VG to guaiacol,
275
suggesting vanillic acid is required for high guaiacol production.
276
release ferulic and p-coumaric acids from steamed rice grains in the sake
277
brewing process,30,33 however the bioconversion ability from ferulic acid to
278
vanillic acid has never been reported.34,35 We analyzed phenolic acid
In sake brewing, ethanol concentration and
Growth and guaiacol formation of S.
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A. oryzae
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production in the rice koji culture, using steamed rice and A. oryzae RIB128.
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Phenolic acids, except ferulic acid, were not detected at the starting point of
281
cultivation, however, phenolic acids, including vanillic acid, were detected during
282
cultivation, until 41 h (Figure 3). It is suggested that the fungi produce the
283
phenolic acids from the degraded compounds of steamed rice.
284
may be converted to vanillic acid by A. oryzae RIB128 and it is possible that
285
other fungi could perform this conversion, including A. niger.36-39 We also
286
cultivated A. oryzae RIB128 on an agar plate containing ferulic acid at 20 mg/L.
287
Vanillic acid was detected on the second day, but the level was very low (< 0.1
288
mg/kg medium) and had disappeared by the third day (data not shown). The
289
difference in culture media might affect vanillic acid production in A. oryzae.
290
Previous analysis of phenolic acids in food rice, whose polishing rate was ca.
291
90 % reported that vanillic acid was found at low levels,40,41 however, we could
292
not detect it in steamed rice grains.
293
milling ratio (60 %) of used rice and the soaking and steaming procedures.
294
Differences in phenolic acid production among A. oryzae strains were also
295
examined (Table 5). All strains tested produced vanillic acid at more than 1.1
296
mg/ kg dry mass koji, indicating that vanillic acid, a precursor of guaiacol, is
297
constantly supplied in the common sake brewing process.
298
General Discussion.
299
at more than ca. 1 mg/kg dry mass koji in the common rice koji culture, and
300
spoilage bacteria, Bacillus sp. and S. gallinarum, present in the rice koji may
301
convert vanillic acid to guaiacol. The vanillic acid level in rice koji and the
302
bioconversion ability of the spoilage bacteria seems to be adequate to account
303
for the existence of guaiacol in sake at sensory significant levels when the
304
spoilage bacteria grow notably. Guiraud et al. reported that A. oryzae converts
Ferulic acid
The difference might be due to a high
This study revealed that A. oryzae produces vanillic acid
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vanillic acid to guaiacol during cultivation when vanillic acid is the sole carbon
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source, however, we did not detect guaiacol in the six rice koji samples listed in
307
Table 1 in spite of the existence of vanillic acid at mg/kg concentrations.
308
observation supported the results of Suezawa et al. who reported that A. oryzae
309
in sake brewing does not form guaiacol from vanillic acid.
310
conditions of the two experiments differed and further studies are required to
311
clarify this point. We believe this is the first report on guaiacol formation in
312
Japanese sake brewing. The results of this study suggested that thorough
313
microbial control is important in rice koji culture to prevent the occurrence of
314
phenolic off-odors in sake.
The cultivation
315 316 317
ASSOCIATED CONTENT
318
Supporting Information
319
Chromatograms used for the identification and quantitation of the volatile
320
phenols (Figure S1) and phenolic acids (Figure S2).
(PDF)
321 322 323
AUTHOR INFORMATION
324
Corresponding Author
325
*(K.H.) Fax: +81-18-872-1676; E-mail:
[email protected] 326
NOTE
327
The authors declare no competing financial interest.
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REFERENCES
14
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Our
Page 15 of 30
Journal of Agricultural and Food Chemistry
331
(1) Rosazza, J.P.N.; Huang, Z.; Dostal, L.; Volm, T.; Rousseau, B. Review:
332
Biocatalytic Transformations of Ferulic Acid: an Abundant Aromatic Natural
333
Product. J. Ind. Microbiol. 1995, 15, 457-471.
334
(2) Huang, Z.; Dostal, L.; Rosazza, P.N. Mechanism of Ferulic Acid Conversions
335
to Vanillic Acid and Guaiacol by Rhodotorula rubura. J. Biol. Chem. 1993, 268,
336
23954-23958.
337
(3)
338
Decarboxylation to Guaiacol. Appl. Environ. Micribiol. 1978, 36, 539-543.
339
(4) Vicuńa, R.; González, B.: Mozuch, M.D.; Kirk, T.K.
340
Model Compounds of the Arylglycerol-ß-Aryl Ether Type by Psedomonas
341
acidovorans D3. Appl. Environ. Micribiol. 1987, 53, 2605-2609.
342
(5) Chow, K.T.; Pope, M.K.; Davis J. Characterization of a Vanillic Acid
343
Non-Oxidative Decarboxylation Gene Cluster from Streptomyces sp. D7.
344
Microbiology 1999, 145, 2393-2403.
345
(6) Álvarez-Rodríguez, M.L.; Belloch, C.; Villa, M.; Uruburu, F.; Larriba, G.;
346
Coque, J-J.R. Degradation of Vanillic Acid and Production of Guaiacol by
347
Microorganisms Isolated from Cork Samples. FEMS Microbiol. Letter 2003, 220,
348
49-55.
349
(7) Chang, S.S.; Kang, D.H. Alicyclobacillus spp. in the Fruit Juice Industry:
350
History, Characteristics, and Current Isolation/Detection Procedures. Crit. Rev. in
351
Microliol. 2004, 30, 55-74.
352
(8) Smit, Y.; Cameron, M.; Venter, P.; Witthuhn, R.C. Alicyclobacillus Spoilage
353
and Isolation – A Review. Food Microbiol. 2011, 28, 331-349.
354
(9) Witthuhn, R.C.; van der Merwe, E.; Venter, P.; Cameron M. Guaiacol
355
Production from Ferulic Acid, Vanillin and Vanillic Acid by Alicyclobacillus
356
acidoterrestris. Int. J. Food Microbiol. 2012, 1578, 113-117.
Crawford,
R.L.;
Olson,
P.P.
Microbial
Catabolism
15
ACS Paragon Plus Environment
of
Vanillate:
Metabolism of Lignin
Journal of Agricultural and Food Chemistry
357
(10) Guillén M.D.; Manzanos, M.J. Study of the Volatile Composition of an
358
Aqueous Oak Smoke Preparation. Food Chem. 2002, 79, 283-292.
359
(11) Pino, J. A. Characterization of volatile Compounds in a Smoke Flavouring
360
from Rice Husk. Food Chem. 2014, 153, 81-86.
361
(12) Prida, A.; Chatonnet, P. Impact Oak-Derived Compounds on the Olfactory
362
Perception of Barrel-Aged Wines. Am. J. Enol. Vitic. 2010, 61, 408-413.
363
(13) de Simón, B.F.; Cadahía, E.; Muiňo, I.; Álamo, M.D.; Nevares, I. Volatile
364
Composition of Toasted Oak Chips and Staves and Red Wine Aged with Them.
365
Am. J. Enol. Vitic. 2010, 61, 157-165.
366
(14) Mayr, C.M.; Parker, M.; Baldock, G.A.; Black, C.A.; Pardon, K.H.; Williamson,
367
P.O., Herderich, M.J.; Francis, I.L. Determination of the Importance of In-Mouth
368
Release of Volatile Phenol Glycoconjugate to the Flavor of Smoke-Tainted
369
Wines. J. Agric. Food Chem. 2014, 62, 2327-2336.
370
(15) Scholtes, C.; Nizet, S.; Collin, S. Guaiacol and 4-Methylphenol as Specific
371
Marker of Torrefied Malts. Fate of Volatile Phenols in Special Beers through
372
Aging. J. Agric. Food Chem. 2014, 62, 9522-9528.
373
(16) Chatonnet, P.; Dubourdieu, D.; Boidron, J.N.; Pons, M. The origin of
374
Ethylphenols in Wine. J. Sci. Food Agric. 1992, 60,165-178.
375
(17) Chatonnet, P.; Dubourdieu, D.; Boidron, J.N.; Lavigne, V. Synthesis of
376
Volatile Phenols by Saccharomyces cerevisiae in Wines. J. Sci. Food Agric.
377
1993, 62, 191-202.
378
(18) Coghe, S.; Benoot, K.; Delvaux, F.; Vanderhaegen, B.; Delvaux, F.R. Ferulic
379
Acid Release and 4-Vinylguaiacol Formation during Brewing and Fermentation:
380
Indications for Feruloyl Esterase Activity in Saccharomyces cerevisiae. J. Agric.
381
Food Chem. 2004, 52, 602-608.
382
(19) Mo, X.; Xu, Y. Ferulic Acid Release and 4-Vinylguaiacol Formation during
16
ACS Paragon Plus Environment
Page 16 of 30
Page 17 of 30
Journal of Agricultural and Food Chemistry
383
Chinese Rice Wine Brewing and Fermentation. J. Inst. Brew. 2010, 116,
384
304-311.
385
(20) Kaneoke, M. 4-Vinylguaiacol Formation in Sake. J. Brew. Soc. Japan 2014,
386
109, 320-326.
387
(21) Sunao, M.; Ito, T.; Hiroshima, K.; Sato, M.; Uehara, T.; Ohno, T.; Watanabe,
388
S.; Takahashi, H.; Hashizume, K. Analysis of Volatile Phenolic Compounds
389
Responsible for 4-Vinylguaiacol-Like Odor Characteristics of Sake. Food Sci.
390
Technol. Res. 2016, 22,111- 116.
391
(22) Goto, K.; Matsubara, H.; Mochida, K.; Matsumura, T.; Hara, Y.; Niwa, M.;
392
Yamasato, K. Alicyclobacillus herbarius sp. Nov., a Novel Bacterium Containing
393
ω-Cycloheptane Fatty Acids, Isolated from Herbal Tea. Int. J. Syst. Envol.
394
Microbiol. 2002, 52, 109-113.
395
(23) Lane, D.J. In Nucleic Acid Techniques in Bacterial Systematics;
396
Stackebrandt, E. and Goodfellow, M. Eds.; John Willy and Sons Ltd. Chichester,
397
1991, pp.115-147.
398
(24) Muyzer, G.; De Wall, E.C.; Uitterlinden, A.G. Profiling of Complex Microbial
399
Populations by Denaturing Gradient Gel Electrophoresis Analysis of Polymerase
400
Chain Reaction-amplified Genes Coding for 16S rRNA. Appl. Environ. Microbiol.
401
1993, 59, 695-700.
402
(25) Paster, B.J.; Dewhirst, F.E.; Olsen, I.; Fraser, G.J.; Phylogeny of Bacteroides,
403
Prevotella, and Porphyromonas spp. and Related Bacteria. J. Bacteriol. 1994,
404
176, 725-732.
405
(26) Suzuki, M.T.; Giovannoni, S.J.; Bias Caused by Template Annealing in the
406
Amplification of Mixtures of 16S rRNA Genes by PCR. Appl. Environ. Microbiol.
407
1996, 62, 625-630.
408
(27) Kaneko, S.; Sakai, R.; Kmuzawa, K.; Usuki, M.; Nishimura, O. Key Aroma
17
ACS Paragon Plus Environment
Journal of Agricultural and Food Chemistry
409
Compounds in Roasted In-shell Peanuts.
410
77, 1467-1473.
411
(28) Wakamatsu, D.; Morimura, S.; Sawa, T.; Kida, K.; Nakai, C.; Maeda, H.
412
Isolation, Identification, and Structure of a Potent Alkyl-Peroxyl Radical
413
Scavenger in Crude Canola Oil, Canolol. Biosci. Biotechnol. Biochem. 2005, 69,
414
1568-1574.
415
(29) Nakamura, K.; Tadenuma, M.; Motegi, K.; Yoshie, T.; Sato, S. Studies on
416
Changes in Color and Flavor of Sake Caused by Exposure to Light and Storage:
417
(IV) Reducing Substances in Rice-Koji. J. Brew. Soc. Japan 1969, 64,
418
1092-1098.
419
(30) Ito, T.; Suzuki, N.; Nakayama, A.; Ito, M.; Hashizume, K. Factors Affecting
420
Phenolic Acid Liberation from Rice Grains in the Sake Brewing Process. J.
421
Biosci. Bioeng. 2014, 118, 640-645.
422
(31) Lupa, B.; Lyon, D.; Shaw, L.N.; Sieprawska-Lupa, M.; Wiegel, J. Properties
423
of the Reversible Nonoxidative Vanillate/ 4-Hydroxybezoate Decarboxylase from
424
Bacillus subtilis. Can. J. Microbiol. 2008, 54, 75-81.
425
(32) Ohta, Y.; Nishi, S.; Haga, T.; Tsubouchi, T.; Hasegawa, R.; Konishi, M.;
426
Nagano, Y.; Tsurukawa, Y.; Shimane, Y.; Mori, K.; Usui, K.; Suda, E.; Tsutui, K.,
427
Nishimoto, A.; Fujiwara, Y.; Maruyama, T.; Hatada, Y. Screening and
428
Phylogenetic Analysis of Deep-Sea Bacteria Capable of Metabolizing
429
Lignin-Derived Aromatic Compounds. Open J. Marine Sci. 2012, 2, 177-187.
430
(33) Hashizume, K; Ito,T.; Nakayama, A.; Okuda, M. Analysis of Ferulic and
431
p-Coumaric Acids in Japanese Rice for Sake Brewing. Cereal Chem. 2014, 91,
432
45-49.
433
(34) Yoshizawa, K.; Komatsu, S.; Takahashi, I.; Otsuka, K. Phenolic Compounds
434
in the Fermented Products Part I. Origin of Ferulic Acid in Saké. Agric. Biol.
Biosci. Biotechnol. Biochem. 2013,
18
ACS Paragon Plus Environment
Page 18 of 30
Page 19 of 30
Journal of Agricultural and Food Chemistry
435
Chem. 1970, 34, 170-180.
436
(35) Suezawa, Y.; Yoshioka, N.; Mori, H. Bioconversion of Ferulic Acid and
437
p-Coumaric Acid to Volatile Phenols by Aspergillus spp. and Bacteria Found in
438
Soy Sauce Koji and Mashies. Nippon Nōgeikagaku Kaishi 1998, 72, 43-49.
439
(36) Rahouti, M.; Seigle-Murandi, F.; Steiman, R.; Eriksoon, K.-E. Metabolism of
440
Ferulic Acid by Paecilomyces variotii and Pestalotia palmarum. Appl. Environ.
441
Micribiol. 1989, 55, 2391-2398.
442
(37) Topakas, E; Kalogeris, E.; Kekos, D.; Macris, B.J.; Christakopoulos, P.
443
Bioconversion of Ferulic Acid into Vanillic Acid by the Thermophilic Fungus
444
Sporotichum thermophile. Lebensm.-Wiss. U-Technol. 2003, 36, 561-565.
445
(38) Lesage-Meessen L.; Delattre, M.; Haon, M.; Thibault, J.F.; Deccaldi, B.C.;
446
Brunerie, P.; Asther, M. A Two-Step Bioconversion Process for Vanillin
447
Production from Ferulic Acid Combining Aspergillus niger and Pycnoporus
448
cinnabarinus. J. Biotechnol. 1996, 50, 107-113.
449
(39) Hegde, S.; Kavitha, S.; Varadaraj, M.C.; Muralikrishna, G. Degradation of
450
Cereal Bran Polysaccharide-Phenolic Acid Complex by Aspergillus niger CFR
451
1105. Food Chem. 2006, 96, 14-19.
452
(40) Tian, S.; Nakamura, K.; Kayahara, H. Analysis of Phenolic Compounds in
453
White Rice, Brown Rice, and Germinated Brown Rice. J. Agric. Food Chem.
454
2004, 52, 4808-4813.
455
(41) Zhou, Z.; Robards, K.; Helliwell, S.; Blanchard, C. The Distribution of
456
Phenolic Acids in Rice. Food Chem. 2004, 87, 401-406.
457
(42) Guiraud, P.; Steiman, R.; Seigle-Murandi, F.; Benoit-Guyod, J.L. Metabolism
458
of Vanillic Acid by Micromycetes. World J. Microbiol. Biotechnol. 1992, 8,
459
270-275.
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FIGURE CAPTIONS Figure 1. a
The junmai-type sake brewing process.
+24 and +2 indicate increases in water.
Numerical values are common and
approximate weight proportions.
Figure 2.
Effects of ethanol concentration (A) and pH (B) on growth and
guaiacol formation of isolated bacteria.
–△-; Absorbance at 660 nm, -■-; Ratio
of conversion from vanillic acid to guaiacol (%).
Data are means ± the S.D. for
triplicated experiments.
Figure 3.
Concentration of phenolic acids in the rice koji cultivation process.
-----; temperature, -●-; vanillic acid, -○-; p-hydroxybenzoic acid, -◇-; p-hydroxyphenylacetic acid, -◆-; p-coumaric acid, -■-; ferulic acid. Data are means ± the S.D. for three measurements.
Table 1. Water and Volatile Phenol Contents of Rice Koji Samples a 4-EG, 3-MP, 4-VG, 4-EP, 2,6-DMP, and 4-VP are 4-ethylguaiacol, 3-methylphenol, 4-vinylguaiacol, 4-ethylphenol, 2,6-dimethoxyphenol, and 4-vinylphnol, respectively. b Data are means ± the S.D. for three measurements.
Table 2. Phenolic Acid Content of Rice Koji Samples [mg/kg dry mass koji] a Data are means ± the S.D. for three measurements.
Table 3. Isolated and Identified Guaiacol Forming Microorganisms from Rice Koji Samples
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Table 4. Phenolic Compound Converting Ability of Identified Microorganisms a Data are means ± the S.D. for triplicated experiments.
Table 5. Effects of Aspergillus oryzae on Phenolic Acid Levels in Rice Koji [mg/kg dry mass koji] a Data are means ± the S.D. for three measurements.
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