Production and partial characterization of polygalacturonases produced by thermophilic Monascus sp N8 and by thermotolerant Aspergillus sp N12 on solid-state fermentation

被引:23
作者
de Freitas, Paula Mendes [1 ]
Martin, Natalia [1 ]
Silva, Denis [1 ]
da Silva, Roberto [1 ]
Gomes, Eleni [1 ]
机构
[1] UNESP, IBILCE, Lab Bioquim & Microbiol Aplicada, BR-15054000 Sao Jose Do Rio Preto, SP, Brazil
关键词
Monascus sp; Aspergillus sp; thermophilic; polygalacturonase; solid-state fermentation; PECTINASES; GROWTH; NIGER;
D O I
10.1590/S1517-83822006000300019
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Polygalacturonases production by newly isolated Monascus sp N8 and Aspergillus sp N12 strains was carried out in solid-state fermentation using mixtures of wheat bran, sugar cane bagasse and orange bagasse as carbon sources. The maximal activity values of exo-polygalacturonases (exo-Pg) from Monascus sp and Aspergillus sp were obtained using wheat bran/sugar cane bagasse/orange bagasse mixture (6.6 U/mL) and wheat bran/orange bagasse mixture (10 U/mL), respectively. Enzyme production by both strains was higher at 45 degrees C after 72 h and 1.6 U/mL at 50 C after 120 h. Endo-polygalacturonase (endo-Pg) production was higher in wheat bran/orange bagasse mixture and was not affected by temperature of incubation for both fungi. Endo-Pg production by Monascus was 1.8 U/mL at 45 degrees C and 50 degrees C, after 72. Similar values were obtained in Aspergillus sp culture, 1.9 U/mL at 45 degrees C and 1.8 U/mL at 50 degrees C. Exo-Pg from both strains showed optimum activity at pH 5.5. Maximal activity was determined at 60 degrees C for enzyme from Monascus sp and 50 C for that produced by Aspergillus sp. Exo-Pg from Monascus sp was stable at pH range 4.5-6.0 whereas that from Aspergillus sp enzyme was stable at pH 4.0. Both enzymes showed stability when incubated at 50 degrees C for 1 h, in absence of substrate.
引用
收藏
页码:302 / 306
页数:5
相关论文
共 18 条
[1]  
Antranikian G., 1992, Microbial degradation of natural products., P27
[2]   STRAIN AND PROCESS FOR PRODUCTION OF POLYGALACTURONASE [J].
BAILEY, MJ ;
PESSA, E .
ENZYME AND MICROBIAL TECHNOLOGY, 1990, 12 (04) :266-271
[3]  
Da-Silva R., 1997, Boletim da Sociedade Brasileira de Ciencia e Tecnologia de Alimentos, V31, P249
[4]   Growth conditions of Aspergillus sp. ATHUM-3482 for polygalacturonase production [J].
GaliotouPanayotou, M ;
Kapantai, M ;
Kalantzi, O .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 1997, 47 (04) :425-429
[5]   ENHANCED POLYGALACTURONASE PRODUCTION BY ASPERGILLUS-NIGER NRRL-364 GROWN ON SUPPLEMENTED CITRUS PECTIN [J].
GALIOTOUPANAYOTOU, M ;
RODIS, P ;
KAPANTAI, M .
LETTERS IN APPLIED MICROBIOLOGY, 1993, 17 (04) :145-148
[6]   Purification and biochemical properties of microbial pectinases - a review [J].
Gummadi, SN ;
Panda, T .
PROCESS BIOCHEMISTRY, 2003, 38 (07) :987-996
[7]  
HANG YD, 1994, FOOD SCI TECHNOL-LEB, V27, P194
[8]   PECTIN TRANS-ELIMINASE WITH FRUIT JUICE CLARIFYING ACTIVITY [J].
ISHII, S ;
YOKOTSUKA, T .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1971, 19 (05) :958-+
[9]   Production, characterization and application of a thermostable polygalacturonase of a thermophilic mould Sporotrichum thermophile Apinis [J].
Kaur, G ;
Kumar, S ;
Satyanarayana, T .
BIORESOURCE TECHNOLOGY, 2004, 94 (03) :239-243
[10]  
Lea A.G.H., 1998, ENZYMES FOOD PROCESS, P223