黑龙江农业科学
黑龍江農業科學
흑룡강농업과학
HEILONGJINAG AGRICULTURAL SCIENCE
2015年
2期
115-117
,共3页
马怀良%陈欢%弥春霞%龚振杰%姜明%孙欢%张靓
馬懷良%陳歡%瀰春霞%龔振傑%薑明%孫歡%張靚
마부량%진환%미춘하%공진걸%강명%손환%장정
高温蒸煮%碳酸钠%碳酸氢钠%破壁%黑木耳
高溫蒸煮%碳痠鈉%碳痠氫鈉%破壁%黑木耳
고온증자%탄산납%탄산경납%파벽%흑목이
stewing%sodium carbonate%sodium bicarbonate%cell disruption%A uricularia auricula Judae
为有效地提取黑木耳中的成分以利于黑木耳深层次开发,以可溶性物质含量为指标,应用均匀设计法研究了高温蒸煮(121℃)时间(20~120 min)、碳酸钠和碳酸氢钠浓度(0~0.5%)对黑木耳破壁的影响。结果表明:可溶性物质(y)与Na2 CO3浓度(x1)和时间(x3)以及NaHCO3浓度(x2)呈函数关系,即 y=-1.3921+135.8644 x1+0.1019 x2-70.2096 x12(R2=0.9928,P<0.01);y=12.9572+154.1617 x22(R2=0.9022, P<0.01)。根据方程理论计算和实际验证,Na2 CO3浓度为0.5%,时间为120 min ,破壁效果最好;NaHCO3浓度为0.5%,破壁效果最好。
為有效地提取黑木耳中的成分以利于黑木耳深層次開髮,以可溶性物質含量為指標,應用均勻設計法研究瞭高溫蒸煮(121℃)時間(20~120 min)、碳痠鈉和碳痠氫鈉濃度(0~0.5%)對黑木耳破壁的影響。結果錶明:可溶性物質(y)與Na2 CO3濃度(x1)和時間(x3)以及NaHCO3濃度(x2)呈函數關繫,即 y=-1.3921+135.8644 x1+0.1019 x2-70.2096 x12(R2=0.9928,P<0.01);y=12.9572+154.1617 x22(R2=0.9022, P<0.01)。根據方程理論計算和實際驗證,Na2 CO3濃度為0.5%,時間為120 min ,破壁效果最好;NaHCO3濃度為0.5%,破壁效果最好。
위유효지제취흑목이중적성분이리우흑목이심층차개발,이가용성물질함량위지표,응용균균설계법연구료고온증자(121℃)시간(20~120 min)、탄산납화탄산경납농도(0~0.5%)대흑목이파벽적영향。결과표명:가용성물질(y)여Na2 CO3농도(x1)화시간(x3)이급NaHCO3농도(x2)정함수관계,즉 y=-1.3921+135.8644 x1+0.1019 x2-70.2096 x12(R2=0.9928,P<0.01);y=12.9572+154.1617 x22(R2=0.9022, P<0.01)。근거방정이론계산화실제험증,Na2 CO3농도위0.5%,시간위120 min ,파벽효과최호;NaHCO3농도위0.5%,파벽효과최호。
In order to effectively extract ingredients and lay a foundation for deep development for fruit bodies of A uricularia auricula Judae ,the method of uniform design was applied to study the effects of high temperature (121℃)stewing time(20~120 min)and concentrations of sodium carbonate or sodium bicarbonate (0~0 .5% ) on cell disruption of fruit bodies indicated by solute contents .The results showed that solute contents (y) had a functional relation with time and concentrations of sodium carbonate ,and concentrations of sodium bicarbon‐ate ,y= -1 .3921+135 .864 4 x1 +0 .101 9 x2 -70 .209 6 x1 2 (R2 =0 .992 8 ,P<0 .01 ) , y=12 .957 2+154 .161 7x22 (R2 =0 .902 2 ,P<0 .01) .Based on theoretical calculations of equations and further actual verifications , the optimum conditions of cell disruption were 120 min and the sodium carbonate concentration was 0 .5% ;so‐dium bicarbonate concentration was 0 .5% ,respectively .