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鞘氨醇单胞菌属菌株TCM1中用于利用阻燃剂磷酸三(2-氯乙基)酯的碱性磷酸酶基因的鉴定。

Identification of alkaline phosphatase genes for utilizing a flame retardant, tris(2-chloroethyl) phosphate, in Sphingobium sp. strain TCM1.

作者信息

Takahashi Shouji, Katanuma Hiroshi, Abe Katsumasa, Kera Yoshio

机构信息

Department of Bioengineering, Nagaoka University of Technology, Nagaoka, Niigata, 940-2188, Japan.

出版信息

Appl Microbiol Biotechnol. 2017 Mar;101(5):2153-2162. doi: 10.1007/s00253-016-7991-9. Epub 2016 Nov 19.

DOI:10.1007/s00253-016-7991-9
PMID:27866252
Abstract

Tris(2-chloroethyl) phosphate (TCEP) is a haloalkyl phosphate flame retardant and plasticizer that has been recognized as a global environmental contaminant. Sphingobium sp. strain TCM1 can utilize TCEP as a phosphorus source. To identify the phosphomonoesterase involved in TCEP utilization, we identified four putative alkaline phosphatase (APase) genes, named SbphoA, SbphoD1, SbphoD2, and SbphoX-II, in the genome sequence. Following expression of these genes in Escherichia coli, APase activity was confirmed for the SbphoA and SbphoX-II gene products but was not clearly observed for the SbphoD1 and SbphoD2 gene products, owing to their accumulation in inclusion bodies. The single deletion of either SbphoA or SbphoX-II retarded the growth and reduced the APase activity of strain TCM1 cells on medium containing TCEP as the sole phosphorus source; these changes were more marked in cells with the SbphoX-II gene deletion. In contrast, the deletion of either SbphoD1 or SbphoD2 had no effect on cell growth or APase activity. The double deletion of SbphoA and SbphoX-II resulted in the complete loss of cell growth on TCEP. These results show that SbPhoA and SbPhoX-II are involved in the utilization of TCEP as a phosphorus source and that SbPhoX-II is the major phosphomonoesterase involved in TCEP utilization.

摘要

磷酸三(2-氯乙基)酯(TCEP)是一种卤代烷基磷酸酯类阻燃剂和增塑剂,已被认定为一种全球环境污染物。鞘氨醇单胞菌属菌株TCM1能够利用TCEP作为磷源。为了鉴定参与TCEP利用的磷酸单酯酶,我们在基因组序列中鉴定出了四个假定的碱性磷酸酶(APase)基因,分别命名为SbphoA、SbphoD1、SbphoD2和SbphoX-II。在大肠杆菌中表达这些基因后,证实SbphoA和SbphoX-II基因产物具有APase活性,但由于SbphoD1和SbphoD2基因产物在包涵体中积累,未明显观察到其APase活性。单独缺失SbphoA或SbphoX-II会阻碍菌株TCM1细胞在以TCEP作为唯一磷源的培养基上的生长,并降低其APase活性;这些变化在缺失SbphoX-II基因的细胞中更为明显。相比之下,缺失SbphoD1或SbphoD2对细胞生长或APase活性没有影响。同时缺失SbphoA和SbphoX-II会导致细胞在TCEP上完全无法生长。这些结果表明,SbPhoA和SbPhoX-II参与了TCEP作为磷源的利用,并且SbPhoX-II是参与TCEP利用的主要磷酸单酯酶。

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