Biochemistry Division, Regional Research Laboratory, Jorhat, Assam, India.
Biotechnol Bioeng. 1991 Jan 5;37(1):1-11. doi: 10.1002/bit.260370103.
The mode of n-hexadecane uptake by two organisms-Pseudomonas M 1 and Pseudomonas N 1-was studied. During the growth of Pseudomonas M 1 on n-hexadecane, no extracellular biosurfactant/bioemulsifier was produced, no significant n-hexadecane pseudosolubilization was observed, and the reduction of surface and interfacial tensions in the cell-free culture broth was negligible. EDTA, a known inhibitor of hydrocarbon pseudosolubilization, did not inhibit the growth of the organism on n-hexadecane. Normal hexadecane-grown cells showed strong surface-active properties and capacity to adhere firmly to hydrocarbon phase. It was concluded that in this organism, surface-active properties of the cells facilitate attachment of cells to the hydrocarbon-water interface generated by agitation, and promote substrate uptake and growth; no hydrocarbon pseudosolubilization or extracellular mediator is involved in the substrate uptake. Pseudomonas N 1 grew on n-hexadecane much faster than Pseudomonas M 1. Growth of this organism on n-hexadecane was associated with the extracellular production of biosurfactant-bioemulsifier and n-hexadecane pseudosolubilizing factor; the growth was strongly inhibited by 5 mM EDTA, indicating that hydrocarbon pseudosolubilization was the dominant factor in substrate uptake. The rate of n-hexadecane pseudosolubilization was high enough to account for the substrate up take rate. Hydrocarbon emulsifying and n-hexadecane pseudosolubilizing factors were isolated and tentatively characterized as lipoprotein and glycoprotein, respectively. Both factors act in a synergistic manner to provide enhanced hydrocarbon transport to cells through pseudosolubilization. It is proposed that this facility of mediated hydrocarbon transport is the basis for the relatively fast rate of growth of Pseudomonas N 1 on hydrocarbon.
两种生物——假单胞菌 M1 和假单胞菌 N1——的正十六烷摄取模式得到了研究。在假单胞菌 M1 利用正十六烷生长的过程中,没有产生细胞外生物表面活性剂/生物乳化剂,没有观察到正十六烷的明显假增溶,且无细胞培养物中表面和界面张力的显著降低。EDTA,一种已知的烃类假增溶抑制剂,没有抑制该生物对正十六烷的生长。正常正十六烷生长的细胞表现出强烈的表面活性特性和牢固地附着在烃相的能力。由此得出结论,在该生物中,细胞的表面活性特性有助于细胞附着在搅拌产生的烃-水界面上,并促进底物的摄取和生长;没有烃类的假增溶或细胞外介质参与底物的摄取。假单胞菌 N1 比假单胞菌 M1 更快地利用正十六烷生长。该生物在正十六烷上的生长与细胞外生物表面活性剂/生物乳化剂和正十六烷假增溶因子的产生有关;该生长受到 5mM EDTA 的强烈抑制,表明烃类的假增溶是底物摄取的主要因素。正十六烷的假增溶速率足以解释底物的摄取速率。烃类乳化和正十六烷假增溶因子被分离并初步鉴定为脂蛋白和糖蛋白,分别。这两种因子以协同作用的方式通过假增溶为细胞提供增强的烃类输送。因此,这种介导的烃类输送的便利设施是假单胞菌 N1 在烃类上相对快速生长的基础。