【目的】筛选一株可以将琼胶转化为新琼寡糖的菌株,并对该菌株进行鉴定。【方法】从紫菜生长区域采集紫菜和该区域海水,用含1‰琼胶的培养基富集培养,逐级稀释涂布、平板划线进行初筛,液体培养进行复筛,DNS法测定琼胶降解产物中还原糖...【目的】筛选一株可以将琼胶转化为新琼寡糖的菌株,并对该菌株进行鉴定。【方法】从紫菜生长区域采集紫菜和该区域海水,用含1‰琼胶的培养基富集培养,逐级稀释涂布、平板划线进行初筛,液体培养进行复筛,DNS法测定琼胶降解产物中还原糖的含量。通过16S r DNA序列分析,结合菌体形态、菌落特征及生理生化特性,确立该菌的系统发育学地位。【结果】从紫菜振荡液中筛选出一株可以产琼胶酶的菌株HJPHYXJ-1,该菌属于革兰氏阴性菌,16S r DNA序列同源性与需钠弧菌(Vibrio natriegens)的达到了99%,结合形态特征和生理生化实验结果鉴定该菌为需钠弧菌。HPLC法测定酶解产物为新琼寡糖。【结论】HJPHYXJ-1被筛选用于转化琼胶,酶解产物的聚合度在2-12之间,是以二糖为单位的新琼寡糖,该菌产生的酶为β-琼胶酶。展开更多
Bacteria growth depends crucially on protein synthesis,which is limited by ribosome synthesis.Ribosomal RNA(rRNA)transcription is the rate-limiting step of ribosome synthesis.It is generally proposed that the transcri...Bacteria growth depends crucially on protein synthesis,which is limited by ribosome synthesis.Ribosomal RNA(rRNA)transcription is the rate-limiting step of ribosome synthesis.It is generally proposed that the transcriptional initiation rate of rRNA operon is the primary factor that controls the r RNA synthesis.In this study,we established a convenient GFP-based reporter approach for measuring the bacterial rRNA chain elongation rate.We showed that the rRNA chain elongation rate of Escherichia coli remains constant under nutrient limitation and chloramphenicol inhibition.In contrast,rRNA chain elongation rate decreases dramatically under low temperatures.Strikingly,we found that Vibrio natriegens,the fastest growing bacteria known,has a 50%higher rRNA chain elongation rate than E.coli,which contributes to its rapid ribosome synthesis.Our study demonstrates that r RNA chain elongation rate is another important factor that affects the bacterial ribosome synthesis capacity.展开更多
文摘【目的】筛选一株可以将琼胶转化为新琼寡糖的菌株,并对该菌株进行鉴定。【方法】从紫菜生长区域采集紫菜和该区域海水,用含1‰琼胶的培养基富集培养,逐级稀释涂布、平板划线进行初筛,液体培养进行复筛,DNS法测定琼胶降解产物中还原糖的含量。通过16S r DNA序列分析,结合菌体形态、菌落特征及生理生化特性,确立该菌的系统发育学地位。【结果】从紫菜振荡液中筛选出一株可以产琼胶酶的菌株HJPHYXJ-1,该菌属于革兰氏阴性菌,16S r DNA序列同源性与需钠弧菌(Vibrio natriegens)的达到了99%,结合形态特征和生理生化实验结果鉴定该菌为需钠弧菌。HPLC法测定酶解产物为新琼寡糖。【结论】HJPHYXJ-1被筛选用于转化琼胶,酶解产物的聚合度在2-12之间,是以二糖为单位的新琼寡糖,该菌产生的酶为β-琼胶酶。
基金the National Natural Science Foundation of China(31700089,31700039,31870028 and 31970027)self-determined research funds of CCNU from the colleges’basic research and operation of MOE(CCNU18KFY01,CCNU19TS028 and CCNU20TS023)。
文摘Bacteria growth depends crucially on protein synthesis,which is limited by ribosome synthesis.Ribosomal RNA(rRNA)transcription is the rate-limiting step of ribosome synthesis.It is generally proposed that the transcriptional initiation rate of rRNA operon is the primary factor that controls the r RNA synthesis.In this study,we established a convenient GFP-based reporter approach for measuring the bacterial rRNA chain elongation rate.We showed that the rRNA chain elongation rate of Escherichia coli remains constant under nutrient limitation and chloramphenicol inhibition.In contrast,rRNA chain elongation rate decreases dramatically under low temperatures.Strikingly,we found that Vibrio natriegens,the fastest growing bacteria known,has a 50%higher rRNA chain elongation rate than E.coli,which contributes to its rapid ribosome synthesis.Our study demonstrates that r RNA chain elongation rate is another important factor that affects the bacterial ribosome synthesis capacity.
