Investigating Synthesis of the MalS Malic Enzyme during Bacillus subtilis Spore Germination and Outgrowth and the Influence of Spore Maturation and Sporulation Conditions

被引:3
|
作者
Swarge, Bhagyashree [1 ,2 ]
Nafid, Chahida [1 ]
Vischer, Norbert [1 ]
Kramer, Gertjan [2 ]
Setlow, Peter [3 ]
Brul, Stanley [1 ]
机构
[1] Univ Amsterdam, Dept Mol Biol & Microbial Food Safety, Amsterdam, Netherlands
[2] Univ Amsterdam, Swammerdam Inst Life Sci, Dept Mass Spectrometry Biomol, Amsterdam, Netherlands
[3] UConn Hlth, Dept Mol Biol & Biophys, Farmington, CT USA
关键词
spore maturation; B; subtilis; MalS; protein synthesis; spore germination; GREEN FLUORESCENT PROTEIN; MEGATERIUM; METABOLISM;
D O I
10.1128/mSphere.00464-20
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Spore-forming bacteria of the orders Bacillales and Clostridiales play a major role in food spoilage and foodborne diseases. When environmental conditions become favorable, these spores can germinate as the germinant receptors located on the spore's inner membrane are activated via germinant binding. This leads to the formation of vegetative cells via germination and subsequent outgrowth and potential deleterious effects on foods. The present report focuses on analysis of the synthesis of the MalS (malic enzyme) protein during Bacillus subtilis spore germina-tion by investigating the dynamics of the presence and fluorescence level of a MalS-GFP (MalS-green fluorescent protein) fusion protein using time-lapse fluorescence microscopy. Our results show an initial increase in MalS-GFP fluorescence intensity within the first 15 min of germination, followed by a discernible drop and stabilization of the fluorescence throughout spore outgrowth as reported previously (L. Si-nai, A. Rosenberg, Y. Smith, E. Segev, and S. Ben-Yehuda, Mol Cell 57:695-707, 2015, https://doi.org/10.1016/j.molcel.2014.12.019). However, in contrast to the earlier report, both Western blotting and SILAC (stable isotopic labeling of amino acids in cell culture) analysis showed there was no increase in MalS-GFP levels during the 15 min after the addition of germinants and that MalS synthesis did not begin until more than 90 min after germinant addition. Thus, the increase in MalS-GFP fluorescence early in germi-nation is not due to new protein synthesis but is perhaps due to a change in the physical environment of the spore cores. Our findings also show that different sporu-lation conditions and spore maturation times affect expression of MalS-GFP and the germination behavior of the spores, albeit to a minor extent, but still result in no changes in MalS-GFP levels early in spore germination. IMPORTANCE The spores formed by Bacillus subtilis remain in a quiescent state for extended periods due to their dormancy and resistance features. Dormancy is linked to a very low level of core water content and a phase-bright state of spores. The present report, focusing on proteins MalS and PdhD (pyruvate dehydrogenase sub-unit D) and complementary to our companion report published in this issue, aims to shed light on a major dilemma in the field, i.e., whether protein synthesis, in particu-lar that of MalS, takes place in phase-bright spores. Clustered MalS-GFP in dormant spores diffuses throughout the spore as germination proceeds. However, fluores-cence intensity measurements, supported by Western blot analysis and SILAC pro-teomics, confirm that there is no new MalS protein synthesis in bright-phase dor-mant spores.
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页数:11
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