Path: news.eternal-september.org!eternal-september.org!feeder3.eternal-september.org!nntp-feed.chiark.greenend.org.uk!ewrotcd!news.eyrie.org!beagle.ediacara.org!.POSTED.beagle.ediacara.org!not-for-mail From: j.nobel.daggett@gmail.com (LDagget) Newsgroups: talk.origins Subject: Re: What is legitimate about the ID bait and switch scam at this =?UTF-8?B?dGltZT8=?= Date: Tue, 17 Jun 2025 18:30:42 +0000 Organization: novaBBS Sender: to%beagle.ediacara.org Approved: moderator@beagle.ediacara.org Message-ID: References: <102kqi6$edbo$1@dont-email.me> <102nmm2$16t4n$1@dont-email.me> <102pfdu$1ntga$1@dont-email.me> <20f638a655d24cf60fc28e80b5dd4819@www.novabbs.com> <102q6fc$1tt7l$1@dont-email.me> <102q91g$1u8t3$1@dont-email.me> <102s87g$2h9el$1@dont-email.me> MIME-Version: 1.0 Content-Type: text/plain; charset=utf-8; format=flowed Content-Transfer-Encoding: 8bit Injection-Info: beagle.ediacara.org; posting-host="beagle.ediacara.org:3.132.105.89"; logging-data="10351"; mail-complaints-to="usenet@beagle.ediacara.org" User-Agent: Rocksolid Light To: talk-origins@moderators.isc.org Return-Path: X-Original-To: talk-origins@ediacara.org Delivered-To: talk-origins@ediacara.org id 18C4B22978C; Tue, 17 Jun 2025 14:36:27 -0400 (EDT) by beagle.ediacara.org (Postfix) with ESMTPS id D75BF229783 for ; Tue, 17 Jun 2025 14:36:24 -0400 (EDT) by moderators.individual.net (Exim 4.98) for talk-origins@moderators.isc.org with esmtp (envelope-from ) id 1uRbAW-000000018Ui-3A0w; Tue, 17 Jun 2025 20:36:24 +0200 id BE9A259803B; Tue, 17 Jun 2025 18:36:21 +0000 (UTC) X-Injection-Info: ; posting-account="fegc7bsF1eMdQ+K4/V59MDLZ0W7qYnKpXoBXaiJNWpk"; X-Rslight-Posting-User: e316cd0a5543fde25fc288f0018b16e943af38c6 X-Rslight-Site: $2y$10$SSu6kLRKQkiNftxZI1XsF.0.ykU.r/wOcvdORmcq/6vz1Yu76Ni8C On Tue, 17 Jun 2025 17:21:50 +0000, RonO wrote: > On 6/17/2025 10:07 AM, LDagget wrote: >> On Mon, 16 Jun 2025 23:23:28 +0000, RonO wrote: >> snippage > What I have always gone by was that when D and L charged tRNAs were in > the mix, translation still proceeded, but more slowly and L amino acids > were still used in making the peptide. I did not recall any type of > controversy involved, but the paper that I linked to noted that it has > never been understood why the D amino acids were not incorporated. As with so much biochemistry, it's complicated when you get into the weeds. Then again, from some perspectives, it's rather simple. The perspective I was weened on is one of kinetics. An aminoacyle tRNA synthetase is an enzyme that, in our modern world, catalyzes the joining of an L-amino acid of the right sort, to a tRNA of the right sort. For example, Metionine aminoacyl tRNA synthetase catalyzes the reaction L-Methionine + tRNA^(Met)(CAU) ==> Met-tRNA^Met(CAU) The ^ indicates the (Met) should be Met written as superscript. (CAU) identifies the anticodon of the tRNA. That's a reasonable description which is a good first order understanding of what happens. Then the fun begins. There is a variant of the amino acids Leucine and Isoleucine called norleucine. These are all amino acids whose R group is C4H9 So for the generic amino acid H2 - N - CH(R) - COOH we roll through different substitutions for R. Leucine R group is -CH(CH3)-CH2-CH3. It branches early. Isoleucine R group is -CH2-C(CH3)2. It branches late. Norleucine R groupis -CH2-CH2-CH2-CH3 It does not branch. Note: Methionine has the R group CH2-CH2-S-CH3 It "looks" just like Norleucine if you swap out the last CH2 for an S. And gosh darn, but Met tRNA synthetase also catalyzes the reaction L-Norleucine + tRNA^(Met)(CAU) ==> Nle-tRNA^Met(CAU) The damned thing apparently didn't read the textbook or attend the lectures. Our understanding is that this happens because the aminoacyl synthetase discriminates according to the shape of the amino acid but methionine and norleucine have very similar shapes. The biotech industry has witnessed significant levels of norleu incorporation in place of met in fermentation products. It's one of those things that repeats in cycles because a new generation comes along who read the textbooks and attended the lectures but didn't listen to old geezers who work for a living. It's always happening at some level. A proper biochemist will think of it this way. The rate at which it happens will depend upon the concentration of L-Met and L-Nle inside the cell synthesizing the protein. If the cells are being fed cheap Purina Cell Chow that has relatively high concentrations of non standard amino acids like Norleucine, it will happen more often. The enzyme Met aminoacyl transferase may even have a 5 or 10 fold preference for Met over Nle, but as synthesis progresses, and the concentration of Met in solution is reduced by incorporation into proteins, the ration of Nle to Met in the cell will increase. Other metabolic pathways will be at work to detect and synthesize more of amino acids whose concentrations dip, and some salvage pathways will consume other amino acids to make more Methionine, including consuming Norleucine, but not instantaneously. Not to belabor it (too late, I know) but similar competition exists with every amino acid tRNA aminoacyl tRNA transferase. The textbook reaction will be 100 fold, or 1000 fold faster for the "right" reaction for equal competing concentration. This will be true for L vs D forms of the same amino acid, or 'similar' amino acids. The specifics of the relative preferences vary. But here the punchline. It's always a competition. There are always side reactions. Enzymes don't read textbooks or attend lectures. They don't know a CORRECT reaction from an INCORRECT reaction. It's the same for DNA synthesis and so mutations happen. If anyone read this far, you're entitled to tell me to shut up. Apologies for being so pedantic.