Water Resources Division, U. S. Geological Survey, 432 National Center, Reston, Virginia 22092, and Department of Biology, George Mason University, Fairfax, Virginia 22030.
Appl Environ Microbiol. 1989 Mar;55(3):700-6. doi: 10.1128/aem.55.3.700-706.1989.
The ability of Alteromonas putrefaciens to obtain energy for growth by coupling the oxidation of various electron donors to dissimilatory Fe(III) or Mn(IV) reduction was investigated. A. putrefaciens grew with hydrogen, formate, lactate, or pyruvate as the sole electron donor and Fe(III) as the sole electron acceptor. Lactate and pyruvate were oxidized to acetate, which was not metabolized further. With Fe(III) as the electron acceptor, A. putrefaciens had a high affinity for hydrogen and formate and metabolized hydrogen at partial pressures that were 25-fold lower than those of hydrogen that can be metabolized by pure cultures of sulfate reducers or methanogens. The electron donors for Fe(III) reduction also supported Mn(IV) reduction. The electron donors for Fe(III) and Mn(IV) reduction and the inability of A. putrefaciens to completely oxidize multicarbon substrates to carbon dioxide distinguish A. putrefaciens from GS-15, the only other organism that is known to obtain energy for growth by coupling the oxidation of organic compounds to the reduction of Fe(III) or Mn(IV). The ability of A. putrefaciens to reduce large quantities of Fe(III) and to grow in a defined medium distinguishes it from a Pseudomonas sp., which is the only other known hydrogen-oxidizing, Fe(III)-reducing microorganism. Furthermore, A. putrefaciens is the first organism that is known to grow with hydrogen as the electron donor and Mn(IV) as the electron acceptor and is the first organism that is known to couple the oxidation of formate to the reduction of Fe(III) or Mn(IV). Thus, A. putrefaciens provides a much needed microbial model for key reactions in the oxidation of sediment organic matter coupled to Fe(III) and Mn(IV) reduction.
腐生极毛杆菌将各种电子供体的氧化与异化 Fe(III) 或 Mn(IV) 还原偶联,从而获得生长所需能量的能力。腐生极毛杆菌可以氢气、甲酸盐、乳酸盐或丙酮酸作为唯一电子供体,并以 Fe(III) 作为唯一电子受体生长。乳酸盐和丙酮酸被氧化为乙酸盐,而乙酸盐不再进一步代谢。当以 Fe(III) 作为电子受体时,腐生极毛杆菌对氢气和甲酸盐具有高亲和力,并且可以在比硫酸盐还原菌或产甲烷菌能够代谢的氢气分压低 25 倍的分压下代谢氢气。Fe(III) 还原的电子供体也支持 Mn(IV) 还原。Fe(III) 和 Mn(IV) 还原的电子供体以及腐生极毛杆菌无法将多碳底物完全氧化为二氧化碳,这将其与已知唯一通过将有机化合物的氧化与 Fe(III) 或 Mn(IV) 的还原偶联来获取生长能量的 GS-15 区分开来。腐生极毛杆菌能够还原大量的 Fe(III),并在确定的培养基中生长,这使其与唯一已知的氢氧化、Fe(III) 还原微生物假单胞菌区分开来。此外,腐生极毛杆菌是已知唯一能够以氢气作为电子供体和 Mn(IV) 作为电子受体生长的生物体,也是已知唯一能够将甲酸盐的氧化与 Fe(III) 或 Mn(IV) 的还原偶联的生物体。因此,腐生极毛杆菌为沉积物有机质氧化与 Fe(III) 和 Mn(IV) 还原偶联的关键反应提供了急需的微生物模型。