Genomics and Ecophysiology of Heterotrophic Nitrogen-Fixing Bacteria Isolated from Estuarine Surface Water

Author:

Bentzon-Tilia Mikkel1ORCID,Severin Ina1,Hansen Lars H.2,Riemann Lasse1

Affiliation:

1. Marine Biological Section, Department of Biology, University of Copenhagen, Helsingør, Denmark

2. Section for Environmental Microbiology and Biotechnology, Department of Environmental Science, Aarhus University, Roskilde, Denmark

Abstract

ABSTRACT The ability to reduce atmospheric nitrogen (N 2 ) to ammonia, known as N 2 fixation, is a widely distributed trait among prokaryotes that accounts for an essential input of new N to a multitude of environments. Nitrogenase reductase gene ( nifH ) composition suggests that putative N 2 -fixing heterotrophic organisms are widespread in marine bacterioplankton, but their autecology and ecological significance are unknown. Here, we report genomic and ecophysiology data in relation to N 2 fixation by three environmentally relevant heterotrophic bacteria isolated from Baltic Sea surface water: Pseudomonas stutzeri strain BAL361 and Raoultella ornithinolytica strain BAL286, which are gammaproteobacteria, and Rhodopseudomonas palustris strain BAL398, an alphaproteobacterium. Genome sequencing revealed that all were metabolically versatile and that the gene clusters encoding the N 2 fixation complex varied in length and complexity between isolates. All three isolates could sustain growth by N 2 fixation in the absence of reactive N, and this fixation was stimulated by low concentrations of oxygen in all three organisms (≈4 to 40 µmol O 2 liter −1 ). P. stutzeri BAL361 did, however, fix N at up to 165 µmol O 2 liter −1 , presumably accommodated through aggregate formation. Glucose stimulated N 2 fixation in general, and reactive N repressed N 2 fixation, except that ammonium (NH 4 + ) stimulated N 2 fixation in R. palustris BAL398, indicating the use of nitrogenase as an electron sink. The lack of correlations between nitrogenase reductase gene expression and ethylene (C 2 H 4 ) production indicated tight posttranscriptional-level control. The N 2 fixation rates obtained suggested that, given the right conditions, these heterotrophic diazotrophs could contribute significantly to in situ rates. IMPORTANCE The biological process of importing atmospheric N 2 is of paramount importance in terrestrial and aquatic ecosystems. In the oceans, a diverse array of prokaryotes seemingly carry the genetic capacity to perform this process, but lack of knowledge about their autecology and the factors that constrain their N 2 fixation hamper an understanding of their ecological importance in marine waters. The present study documents a high variability of genomic and ecophysiological properties related to N 2 fixation in three heterotrophic isolates obtained from estuarine surface waters and shows that these organisms fix N 2 under a surprisingly broad range of conditions and at significant rates. The observed intricate regulation of N 2 fixation for the isolates indicates that indigenous populations of heterotrophic diazotrophs have discrete strategies to cope with environmental controls of N 2 fixation. Hence, community-level generalizations about the regulation of N 2 fixation in marine heterotrophic bacterioplankton may be problematic.

Publisher

American Society for Microbiology

Subject

Virology,Microbiology

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3