Chigaleĭchik A G, Pirieva D A, Rydkin S S
Prikl Biokhim Mikrobiol. 1976 Jul-Aug;12(4):581-6.
The chitinase biosynthesis was studied during the cultivation of the strain of Serratia marcescens BKM B-851 with a high chitinolytic activity. Under submerged cultivation of bacterial cells on the medium containing demineralized crab shell extracellular chitinase showed maximum activity on the 3rd day. Cells of S. marcescens BKM B-851 synthesized chitinase as an adaptive enzyme. Chitinase obtained from the culture liquid by ammonium sulphate precipitation was then dialyzed and liophylized. It displayed optimum hydrolysis of colloid chitin at pH 7-8 and 50 degrees C and of native chitin at 30 degrees C.
在培养具有高几丁质分解活性的粘质沙雷氏菌BKM B - 851菌株的过程中,对几丁质酶的生物合成进行了研究。在含有脱矿蟹壳的培养基上对细菌细胞进行深层培养时,胞外几丁质酶在第3天显示出最大活性。粘质沙雷氏菌BKM B - 851的细胞将几丁质酶合成为一种适应性酶。然后通过硫酸铵沉淀从培养液中获得几丁质酶,接着进行透析和冻干。它在pH 7 - 8和50℃时对胶体几丁质具有最佳水解作用,在30℃时对天然几丁质具有最佳水解作用。