农业环境科学学报
農業環境科學學報
농업배경과학학보
Journal of Agro-Environment Science
2015年
7期
1384-1391
,共8页
刘晓梅%邹亚杰%胡清秀%杨小红%沈德龙
劉曉梅%鄒亞傑%鬍清秀%楊小紅%瀋德龍
류효매%추아걸%호청수%양소홍%침덕룡
菌渣%纤维素降解菌%筛选%16S rDNA序列%酶活力%复合菌剂%堆肥
菌渣%纖維素降解菌%篩選%16S rDNA序列%酶活力%複閤菌劑%堆肥
균사%섬유소강해균%사선%16S rDNA서렬%매활력%복합균제%퇴비
spent substrate%cellulose degrading microorganisms%screening%16S rDNA sequence%enzymatic activity%complex bacteria%compost
为了寻找高效纤维素降解菌,提高菌渣堆肥微生物发酵效果,促进菌渣高效循环利用,从不同地点堆放的杏鲍菇菌渣中采集样品,利用羧甲基纤维素钠培养基分离纤维素降解菌,结合纤维素刚果红水解圈测定、滤纸条降解试验和纤维素酶(滤纸酶FPA、内切葡聚糖酶CMCase、外切葡聚糖酶C1、葡萄糖苷酶β-Gase)活性测定,筛选到4株(FB7、CB1、BC11、BC12)具有高效纤维素降解能力的细菌,经16S rDNA序列分析,鉴定FB7、CB1为枯草芽孢杆菌,BC11为链霉菌属Streptomyces albus,BC12是丛毛单胞菌属的Comamonas jiangduensis,其中FB7降解能力强,可将滤纸条降解成糊状(10d),纤维素酶活力很高,摇瓶发酵4d后FPA、CMCase、C1酶、β-Gase的酶活分别为22.81、314.50、2.78、188.09 U·g-1。复合菌剂CB1+BC11+FB7的FPA、CMCase、C1酶、β-Gase的酶活高于其他各组合,为31.56、133.63、2.31、217.21 U·g-1,与FB7相比分别提高了38.4%、11.2%、178%、70.3%,将复合菌CB1+BC11+FB7接种到菌渣堆肥中,与对照相比,能快速提高堆体温度,且在翻堆后能更好地维持堆温。
為瞭尋找高效纖維素降解菌,提高菌渣堆肥微生物髮酵效果,促進菌渣高效循環利用,從不同地點堆放的杏鮑菇菌渣中採集樣品,利用羧甲基纖維素鈉培養基分離纖維素降解菌,結閤纖維素剛果紅水解圈測定、濾紙條降解試驗和纖維素酶(濾紙酶FPA、內切葡聚糖酶CMCase、外切葡聚糖酶C1、葡萄糖苷酶β-Gase)活性測定,篩選到4株(FB7、CB1、BC11、BC12)具有高效纖維素降解能力的細菌,經16S rDNA序列分析,鑒定FB7、CB1為枯草芽孢桿菌,BC11為鏈黴菌屬Streptomyces albus,BC12是叢毛單胞菌屬的Comamonas jiangduensis,其中FB7降解能力彊,可將濾紙條降解成糊狀(10d),纖維素酶活力很高,搖瓶髮酵4d後FPA、CMCase、C1酶、β-Gase的酶活分彆為22.81、314.50、2.78、188.09 U·g-1。複閤菌劑CB1+BC11+FB7的FPA、CMCase、C1酶、β-Gase的酶活高于其他各組閤,為31.56、133.63、2.31、217.21 U·g-1,與FB7相比分彆提高瞭38.4%、11.2%、178%、70.3%,將複閤菌CB1+BC11+FB7接種到菌渣堆肥中,與對照相比,能快速提高堆體溫度,且在翻堆後能更好地維持堆溫。
위료심조고효섬유소강해균,제고균사퇴비미생물발효효과,촉진균사고효순배이용,종불동지점퇴방적행포고균사중채집양품,이용최갑기섬유소납배양기분리섬유소강해균,결합섬유소강과홍수해권측정、려지조강해시험화섬유소매(려지매FPA、내절포취당매CMCase、외절포취당매C1、포도당감매β-Gase)활성측정,사선도4주(FB7、CB1、BC11、BC12)구유고효섬유소강해능력적세균,경16S rDNA서렬분석,감정FB7、CB1위고초아포간균,BC11위련매균속Streptomyces albus,BC12시총모단포균속적Comamonas jiangduensis,기중FB7강해능력강,가장려지조강해성호상(10d),섬유소매활력흔고,요병발효4d후FPA、CMCase、C1매、β-Gase적매활분별위22.81、314.50、2.78、188.09 U·g-1。복합균제CB1+BC11+FB7적FPA、CMCase、C1매、β-Gase적매활고우기타각조합,위31.56、133.63、2.31、217.21 U·g-1,여FB7상비분별제고료38.4%、11.2%、178%、70.3%,장복합균CB1+BC11+FB7접충도균사퇴비중,여대조상비,능쾌속제고퇴체온도,차재번퇴후능경호지유지퇴온。
The cellulose in spent substrate of edible mushroom is often a limiting factor of the spent substrate decomposition. This study was performed to isolate highly effective cellulose-degrading bacteria from spent substrate in order to improve the fermentation of spent substrate of edible mushroom. Samples were collected from spent substrates of Pleurotus eryngii at different stacking places. Four strains(FB7, CB1, BC11 and BC12)with high cellulose-degrading efficiencies were obtained based on the results of Congo red cellulose hydrolytic hole mea-surement, filter paper degradation test and cellulose activity assays(filter paper enzyme FPA, endoglucanase CMCase, exoglucanase C1 and glucosidaseβ-Gase), using CMC-Na as sole carbon source. 16S rDNA sequencing showed that the trains FB7 and CB1 were Bacillus sub-tilis,thestrainBC11wasStreptomycesalbus,andthestrainBC12wasComamonas jiangduensis.ThestrainFB7withhighfilterpaperde-grading ability had high cellulose activities and degraded filter paper into paste within 10 days. The activities of four enzymes(FPA, CM-Case, C1 andβ-Gase)produced by the stain FB7 cultured for 4 days on a shaking incubator were 22.81 U·g-1, 314.50 U·g-1, 2.78 U·g-1 and 188.09 U·g-1, respectively. The FPA, CMCase, C1, andβ-Gase activities of bacterial combination(CB1+BC11+FB7)were 31.56 U·g-1, 133.61 U·g-1, 2.31 U·g-1, and 217.21 U·g-1, increased by 38.4%, 11.2%, 178%, and 70.3%, respectively, compared with the strain FB7 alone. Inoculation of bacterial combination(CB1+BC11+FB7)to spent substrate compost increased the temperature of the compost quickly, with higher and lesser fluctuations than in the control.