Upload
phamthu
View
213
Download
0
Embed Size (px)
Citation preview
')I58151 km. si 19 alI%/ 1 squ1uw 2539
Drying of Shiitake Mushroom : Effect of Drying on
Lenthionine Content
Charoenkwan Vanabordeenimit’, Sakarindr Bhumiratana2,
Tipaporn Yoovidhya3 and Naphaporn Rattanasomboon4
King Mongkut’s Institute of Technology Thonburi
Abstract
The objective of this research was to study the drying rate and the effect of
drying on the quality with consideration on lenthionine; the specific flavor of shiitake
mushroom. The result indicated that the rate of drying was significantly affected by
temperature and the experimental model used for prediction the drying rate fit reasonable
well with the experimental data. For the analysis of lenthionine, the method was modified
as follows, :- dried shiitake mushroom was left in distilled water at 60°C for 30 min.
and then extracted with hexanes using soxhlet method. The quantity of lenthionine in
the extracted solvent was determined by gas chromatography. The amount of lenthionine
foundinfreshanddriedshiitakemushroomwere2.78x10-5and3.84-8.92x10-5g/gdb.
mushroom, respectively. This indicated that the drying process affected the quantity of
lenthionine. The result of drying at various conditions showed that the quantity of
lenthionine decreased with the increase in the temperature and time. For the step change
in temperature during drying process, 40°C for 6 hours and then 60°C for another 6
hours, the amount of mushroom flavor was higher than that was developed by the
constant drying condition.
’ Graduate Student, Department of Food Engineering
’ Associate Professor, Department of Food Engineering
3 Assistant Professor, Department of Food Engineering
’ Lecturer, Department of Food Engineering
3151157 mix an" 19 au'd1 i%pmJu 2539
4. Ltdba Soxtec d& Tecator system HT2, Extraction unit $J 1045, Service
unit =@ 1044 Lla:: Cool-Ace d&l EYELA iU CA-101
5. dadkh+.n~~ft51~ &k Shimudzu Model 9A tLi% Integrator d&l
Shimudzu Model CR-3A ~GIU%? FID (Flame Ionization Detectors) %tWl&hJltU
~ls~a~auZ~uaJal5a=al~ nait%.diIAwnl53~n5lzti tbu~aihhYa itXuchp~ff
fWWlU1~ 3 NJ. FWn.JEll1 1.6 LUFl5 U55yhEl OV-17 UU Chromasorb WAW/DCMS
80/100 mesh
8 0
Tl5115-l R95. ad 19 mkd 1 ikp1EJu 2539
GI’IYI& 3. ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ Exponential
qaw-$, oswwzfat?_&i MR = exp (-k,t) r2
(awlt~aSu)k2
40 (313.15) 0.463 0.992
50 (323.15) 0.585 0.989
60 (333.15) 0.848 0.998
70 (343.15) 1.137 0.998
85
375a15-l m5. ad 19 QlG 1 ijfyElu 2539
:
:.g 0.6 :5E! :3.$ 0.4 ;;
:::
0.2 I ii‘.
*.4
‘WO-
-*._r _ _ _ _ _ _
0.8
.g 0 . 6E
3 0 . 4zz
0.2
l Data60C
:
i.
n Data 70 C
a7
7158751 i=FJ5. ai 19 inki 1 ihy1uu 2539
sena73s795il1. Morita, K. Kobayashi, S., 1966, “Isolation and Synthesis of Lenthionine and Odorous
Su$stance of Shiitake, an Edible Mushroom,” Tetrahedron Letters, No.6, pp.5 7 3- 5 77.
2. Ito, Y., Toyoda, M., Sezuki, H. andIwaida, M., 1978, “Gas-Liquid Chromatography
of Lenthionine in Shiitake Mushroom (Lentinus edodes) with Special Reference to
the Relation between Carbondisulfide and Lentionine,” Journal of Food Science,
Vo1.43, No.4, pp.1287-1289.
3. Yasumoto, K., Iwami, K. and Mitsuda, H., 1971, “A New Sulfur Containing
Peptide from Lentinus edodes Acting as Precursor for Lenthionine,” Agricultural and
Biological Chemistry, Vol.35, No.13, pp. 2059-2069.
4. Yasumoto, K. and Mitsuda, H., 197 1, “Enzyme-Catalized Evolution of
Lenthionine from Lentinic Acid,” Agricultural and Biological Chemistry,
Vo1.35, No.13, pp. 2072-2080.
88