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1 rized a member of the YrbG family, MaX1 from Methanosarcina acetivorans.
2 mp loader (RFC) from the mesophilic archaeon Methanosarcina acetivorans.
3 e family from the methane-producing archaeon Methanosarcina acetivorans.
4 d in Escherichia coli expressing pylBCD from Methanosarcina acetivorans.
5 methyltransferase MtmB1, was introduced into Methanosarcina acetivorans.
6 a new form of clamp loader from the archaeon Methanosarcina acetivorans.
7 MaPgb from the strictly anaerobic methanogen Methanosarcina acetivorans.
8 ogs, RPA1, RPA2, and RPA3, from the archaeon Methanosarcina acetivorans.
9 on the naturally occurring plasmid pC2A from Methanosarcina acetivorans.
10 genic growth on methylamines in the archaeon Methanosarcina acetivorans.
11 opy (cryo-EM) structure of the ribosome from Methanosarcina acetivorans, a previously unreported high
12                                              Methanosarcina acetivorans, a strictly anaerobic methane
13 ization of an unusual flavodoxin (FldA) from Methanosarcina acetivorans, an acetate-utilizing methane
14 old/one zinc finger replication protein A in Methanosarcina acetivorans and Methanopyrus kandleri exh
15 ence of Methanosarcina barkeri with those of Methanosarcina acetivorans and Methanosarcina mazei.
16 nesis, methyl-coenzyme M reductase (MCR), in Methanosarcina acetivorans and tested whether its cellul
17 iogenesis in the model methanogenic archaeon Methanosarcina acetivorans, and have also identified sub
18 nococcus jannaschii, Archaeoglobus fulgidus, Methanosarcina acetivorans, and Methanosarcina barkeri p
19 chaeoglobus fulgidus, Methanopyrus kandleri, Methanosarcina acetivorans, and Methanosarcina mazei.
20 hlorobaculum tepidum, Magnetococcus marinus, Methanosarcina acetivorans, as well as revisiting the si
21 e isozymes of methanol methyltransferases in Methanosarcina acetivorans C2A and are among the most hi
22          The mtaA1, mtaA2, and mtbA genes of Methanosarcina acetivorans C2A encode putative methanol-
23                                              Methanosarcina acetivorans C2A encodes three putative hy
24                                              Methanosarcina acetivorans C2A is able to convert severa
25 clones were isolated after transformation of Methanosarcina acetivorans C2A with the mutagenized plas
26 en in this process, we tested the ability of Methanosarcina acetivorans C2A, a metabolically versatil
27 oson mutagenesis of a methanogenic archaeon, Methanosarcina acetivorans C2A, which because of its ind
28                The corresponding mutation in Methanosarcina acetivorans C2A, which cannot grow on H(2
29 sequence of an acetate-utilizing methanogen, Methanosarcina acetivorans C2A.
30 ere the first use of directed mutagenesis in Methanosarcina acetivorans C2A.
31 s and characterized the encoded enzymes from Methanosarcina acetivorans C2A.
32  a methanogen into an acetogen and show that Methanosarcina acetivorans can dispense with methanogene
33 lyses to study the structure/function of the Methanosarcina acetivorans clamp loader or replication f
34 rolysine, a 761 base-pair genomic segment in Methanosarcina acetivorans containing the pylT gene (enc
35 ed a markerless tRNA(Pyl) deletion strain of Methanosarcina acetivorans (DeltapylT) that cannot decod
36 bacterial Cas9 protein for genome editing in Methanosarcina acetivorans, enabling efficient gene dele
37                                The genome of Methanosarcina acetivorans encodes three homologs, initi
38              Interestingly, the euryarchaeon Methanosarcina acetivorans harbors multiple functional R
39                       Unlike most organisms, Methanosarcina acetivorans harbors multiple functional R
40                                          The Methanosarcina acetivorans hdrED1 operon is constitutive
41 on of the slow-growing methanogenic archaeon Methanosarcina acetivorans Introduction of both insertio
42 multiheme c-type cytochrome called MmcA from Methanosarcina acetivorans is important for intracellula
43 ation of McrA from the methanogenic archaeon Methanosarcina acetivorans lacking tfuA and/or ycaO reve
44 t comparison of histones from M. jannaschii, Methanosarcina acetivorans (largest Archaeal genome, 5.8
45 se 1 operons (mtaCB1, mtaCB2, and mtaCB3) in Methanosarcina acetivorans led to the suggestion that ea
46 ere identified in M. jannaschii (Mj0601) and Methanosarcina acetivorans (Ma2851), and recombinant Ma2
47 TLPs from Bacillus thuringiensis (BtTLP) and Methanosarcina acetivorans (MaTLP) display biochemical p
48 onsible for formation of S-methylcysteine in Methanosarcina acetivorans McrA.
49 n methanol-grown cells of the marine isolate Methanosarcina acetivorans metabolically labeled with 14
50                        The regulation of the Methanosarcina acetivorans mtsD, mtsF and mtsH genes, wh
51 onance analyses to establish histidine-43 of Methanosarcina acetivorans NifB (MaNifB) as the nitrogen
52 containing NifB protein upon coexpression of Methanosarcina acetivorans nifB, nifS, and nifU genes al
53  naturally "truncated" homologs of NifB from Methanosarcina acetivorans (NifB(Ma)) and Methanobacteri
54 standing of this family, a flavoredoxin from Methanosarcina acetivorans of the Archaea domain was pro
55                                       As the Methanosarcina acetivorans PFOR is comprised of multiple
56                            Here we show that Methanosarcina acetivorans possesses three operons encod
57                                              Methanosarcina acetivorans produces acetate, formate, an
58 , 3046 unique peptides covering 566 distinct Methanosarcina acetivorans proteins were identified from
59 tandem polypeptide repeats that comprise the Methanosarcina acetivorans S-layer protein and propose a
60 haea and that the polymerase from mesophilic Methanosarcina acetivorans shows identical behaviour.
61                                              Methanosarcina acetivorans strain C2A is a marine methan
62                                              Methanosarcina acetivorans strains bearing deletions of
63 ein the purification and characterization of Methanosarcina acetivorans subunit D in complex with sub
64 SH) on >14 500 archaeal and bacterial cells (Methanosarcina acetivorans, Sulfolobus acidocaldarius an
65 MacDinB-1, the homolog from the euryarchaeon Methanosarcina acetivorans that is characterized in this
66                                          The Methanosarcina acetivorans Thg1 (MaThg1) gene contains a
67 otein overproduction system was developed in Methanosarcina acetivorans to facilitate biochemical cha
68 ein 10 gene in the methane-producing archaea Methanosarcina acetivorans Using an array of approaches,
69     Here, we study the methanogenic archaeon Methanosarcina acetivorans using assays of ATP hydrolysi
70      Gene-deletion and growth experiments in Methanosarcina acetivorans, using sulfide as the sole su
71 ltisubunit sodium/proton antiporter (Mrp) of Methanosarcina acetivorans was investigated with a mutan
72 rotein MA4561 from the methanogenic archaeon Methanosarcina acetivorans was originally predicted to b
73                     In the model methanogen, Methanosarcina acetivorans, we demonstrate that the UAG
74 a representative of this new group of RPA in Methanosarcina acetivorans, we made two deletion mutants
75 ologs (TBP1, TBP2, and TBP3) in the archaeon Methanosarcina acetivorans were investigated by using ge
76  termed Hsp60-4 and Hsp60-5, in the archaeon Methanosarcina acetivorans, which also has Hsp60-1, Hsp6
77                   Here, the role of SufBC in Methanosarcina acetivorans, which contains two sufCB gen