吉林农业大学学报
吉林農業大學學報
길임농업대학학보
JOURNAL OF JILIN AGRICUL TURAL UNIVERSITY
2014年
2期
171-175
,共5页
吴海燕%金荣德%范作伟%胡会军%孙甜田%赵兰坡
吳海燕%金榮德%範作偉%鬍會軍%孫甜田%趙蘭坡
오해연%금영덕%범작위%호회군%손첨전%조란파
解磷巨大芽孢杆菌%代谢产物%葡萄糖酸
解燐巨大芽孢桿菌%代謝產物%葡萄糖痠
해린거대아포간균%대사산물%포도당산
Bacillus megaterium%metabolite%gluconic acid
从松辽平原玉米带中部的公主岭市贫磷黑土中分离筛选了1株具有较强溶磷能力的菌株,并通过16S rRNA基因测序鉴定为解磷巨大芽孢杆菌(Bacillus megaterium)。测定了溶磷圈和发酵液有效磷质量分数,探讨了菌株溶磷机理。结果表明:该菌株在以磷酸钙为唯一磷源的培养基上,能够形成明显的溶磷圈;发酵培养到第4天,发酵液的有效磷质量分数达到420 mg/kg。通过粒子大小分析仪,测定了溶磷菌发酵液中的磷酸钙颗粒大小,对照处理的磷酸钙粒径为132.7~181.7 nm,溶磷菌液处理的磷酸钙粒径为77.5~124.2 nm,磷酸钙颗粒明显变小;通过高效液相色谱法(HPLC)和傅里叶变换红外光谱分析仪(FTIR),对溶磷菌发酵液代谢产物进行分析,确定了溶磷菌最终的发酵产物为葡萄糖酸。
從鬆遼平原玉米帶中部的公主嶺市貧燐黑土中分離篩選瞭1株具有較彊溶燐能力的菌株,併通過16S rRNA基因測序鑒定為解燐巨大芽孢桿菌(Bacillus megaterium)。測定瞭溶燐圈和髮酵液有效燐質量分數,探討瞭菌株溶燐機理。結果錶明:該菌株在以燐痠鈣為唯一燐源的培養基上,能夠形成明顯的溶燐圈;髮酵培養到第4天,髮酵液的有效燐質量分數達到420 mg/kg。通過粒子大小分析儀,測定瞭溶燐菌髮酵液中的燐痠鈣顆粒大小,對照處理的燐痠鈣粒徑為132.7~181.7 nm,溶燐菌液處理的燐痠鈣粒徑為77.5~124.2 nm,燐痠鈣顆粒明顯變小;通過高效液相色譜法(HPLC)和傅裏葉變換紅外光譜分析儀(FTIR),對溶燐菌髮酵液代謝產物進行分析,確定瞭溶燐菌最終的髮酵產物為葡萄糖痠。
종송료평원옥미대중부적공주령시빈린흑토중분리사선료1주구유교강용린능력적균주,병통과16S rRNA기인측서감정위해린거대아포간균(Bacillus megaterium)。측정료용린권화발효액유효린질량분수,탐토료균주용린궤리。결과표명:해균주재이린산개위유일린원적배양기상,능구형성명현적용린권;발효배양도제4천,발효액적유효린질량분수체도420 mg/kg。통과입자대소분석의,측정료용린균발효액중적린산개과립대소,대조처리적린산개립경위132.7~181.7 nm,용린균액처리적린산개립경위77.5~124.2 nm,린산개과립명현변소;통과고효액상색보법(HPLC)화부리협변환홍외광보분석의(FTIR),대용린균발효액대사산물진행분석,학정료용린균최종적발효산물위포도당산。
One strain of bacterium with strong phosphate solubilizing activity was isolated from phosphorus deficiency black soil samples in corn belt of the Songliao plain of Northeast China and identified as Bacil-lus megaterium by 1 6s rRNA gene sequencing .The soluble-P concentration continuously increased during the incubation periods and the total amount of soluble P released in culture filtrate was detected at 420 mg/kg after 4 days of inoculation .The particle size of calcium phosphorus surface was found to be destroyed and the size changed between 77.5-1 24.2 nm,while no changes in the surface and size were found in the control with the size of 1 32.7-1 81.7 nm .The metabolites of phosphate solubilizing bacteria fermentation broth were analyzed by high-performance liquid chromatograph (HPLC)and Fourier trans-form infrared spectrometer (FTIR)to determine the final fermentation products of phosphorus solubilizing bacteria for gluconic acid .