cellulose extract 中文意思是什麼
cellulose extract
解釋
亞硫酸紙漿廢液膏-
Quantitative analysis procedure of lignocellulose solid substrate including hemicellulose, cellulose and lignin, ignition method, volumetric method and soak extract method were utilized to study the changes of chemical components in lawn - grass and weeds during hydrothermal degradation with different conditions
摘要運用木質纖維素固體基質半纖維素、纖維素和木質素定量分析程序等分析檢測了不同濕解工況下草坪草和雜草主要組分的化學變化。 -
Tree ring is a kind of natural archives, on which the isotopic analysis is important to study global climate and environmental change. the authors mainly provide a comprehensive introduction to the fractionation models of carbon, hydrogen and oxygen isotope in plants, their research techniques and the extract methods from cellulose. that results show isotopic tracer can record the message of climatic variation and has become a powerful tool for paleoclimate reconstruction and for the modern environment changing research. especially studying on pages, the cellulose isotopic analyses of imbedded old tree ring have become the mainly quantitative means of environmental evolvement. in addition, china is a typical monsoon country, research in tree ring stable isotope seasonal variation can give us a lot of important information on that. up to now, the research techniques and works on tree ring in our country are still in its earlier stage, and remain many limitations. it needs further accumulate basic research materials, intensify regional contrast and intercross studies on relative subjects
尤其是在過去全球變化pages研究中，埋藏古木纖維素中的碳氫氧同位素分析已成為環境演化研究的主要量化手段。另外，對于中國這樣典型的季風氣候國家，開展樹輪穩定同位素隨季節性變化的研究具有重要的意義。我國在樹輪研究方面起步較晚，研究方法和研究內容上也比較簡單，還存在不小差距，既要進一步積累基礎資料，又要做區域對比，加強與相關學科的交叉研究。 -
3. 2. 1. 4 ) which was prepared by precipitation of the water extract of the culture of aspergillus niger with ammonium sulfate and desalted by sephadex g - 25, and was further fractionated by two steps of deae - toyopearl 650m and one step of poros 20pi chromatography. the other was a p - glucosidase ( ec. 3. 2. 1. 21 ) which was prepared by the above g - 25 fractions and was further fractionated by two steps of deae - toyopearl 650m chromatography. the specific activity of the endoglucanase with sodium carboxymethyl cellulose was estimated to be 433. 38 hj / mg
-葡萄糖苷酶對水楊素的比活力為597 . 12iu mg ，並對其專一，不能水解棉花和羧甲基纖維素鈉；分子量為117 . 5kda ，加dtt後分子量不變；該組分最適ph和溫度分別為4 . 5和70 ，在ph5 . 0 、 50下對水楊素鈉的米氏常數km為3 . 73mg ml ，最大反應速度vm為0 . 088mg葡萄糖（ ml ? min ） ；與文獻中從黑麴黴中分離的-葡萄糖苷酶比較后發現，該組分是一個新的-葡萄糖苷酶。 -
The isolation and purification of dnaase in the earthworm the earthworm dnaase was purified from the tissue extract of earthworm by denaturing the protein with low ph buffer, high temperature, ammonium sulfate precipitation, deae - cellulose ( de52 ) chromatography and ultra - filter membrane
雙胸蚓組織中dna酶的分離純化雙胸蚓組織粗提取液經過選擇性酸變性、選擇性熱變性、硫酸按分段鹽析、 deae一纖維素（ de52 ）柱層析、超濾膜分級分離后得到一個電泳純的dna酶。 -
To isolate and purify dnaase in the earthworm first, the tissue extract of earthworm was prepared by dissolving the earthworm with sucrose and denaturing the protein with low ph buffer. then dnaase was purified by denaturing the protein with higher temperature. the following steps were ammonium sulfate precipitation, deae - cellulose ( de52 ) chromatography and filtration by ultra - filter membrane
雙胸蚓組織中dna酶的分離純化採用蔗糖溶解雙胸蚓，並選擇性酸變性制備雙胸蚓組織粗提取液，再經選擇性熱變性、硫酸銨分段鹽析、 deae ?纖維素（ de52 ）柱層析及超濾膜分級分離對雙胸蚓組織中dna酶進行分離純化。 -
The enzyme was purified from cell extract by ammonium sulfate fractionation ( 30 % - 80 % saturation ) and consecutive column chromatography using deae - cellulose and sephadex g - 100. the sod activity for purified enzyme could reach 4966 iu / mg proteins, and the molecular weight of the sod was about 20 kda which determined by sds - page electrophoresis. when the non - denaturing polyacrylamide gel stained with substrate for sod in the present of 0. 2mmol / l kcn or 0. 5 mmol / l h2o2, the active band was still showed at the same position, which indicated the sod could not be inhibited by the treatments with kcn or h2o2 and it was the mn sod
通過sds一聚丙烯酸胺凝膠電泳可知該sod酶的分子量約為20kda .在非變性聚丙烯酞胺凝膠（ pagb ）電泳后，在凝膠son顯色反應液中加入0 . 2耐01 / lkcn或0 . 5inmol / lh202 ，凝膠sod顯色反應后在原來的sod酶部位仍然含有sod活性帶，這表明利用kcn和h20 :處理並不能抑制500的活性，該sod屬于mn一sod 。
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